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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (4) Show 4 proteins XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-06 15:16:49 UTC

Update Date

2022-03-07 02:51:37 UTC

HMDB ID

HMDB0014429

Secondary Accession Numbers

HMDB14429

Metabolite Identification

Common Name

Acarbose

Description

An inhibitor of alpha glucosidase that retards the digestion and absorption of carbohydrates in the small intestine and hence reduces the increase in blood-glucose concentrations after a carbohydrate load. It is given orally to non-insulin dependent diabetes mellitus patients where diet modification or oral hypoglycemic agents do not control their condition. (From Martindale The Extra Pharmacopoeia, 31st ed)

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

ChEBI
  Mrv0541 02231214342D          

 44 47  0  0  1  0            999 V2000
   14.2149   -7.4046    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.6151   -6.6931    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.3515   -7.4157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.6299   -8.1123    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.4414   -6.6857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.1926   -5.9818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5289   -7.4231    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.4525   -8.1087    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.2223   -8.8312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8638   -7.3935    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.6076   -5.2629    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1176   -8.1383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.1064   -6.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8675   -8.8164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.6864   -7.3824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2949   -8.1458    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.5326   -8.8497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2801   -6.7228    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.5349   -7.3639    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.8799   -7.4379    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.8873   -8.8683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8577   -6.0113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9426   -6.6488    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.9463   -8.0716    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.1166   -7.4788    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   18.7652   -6.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5201   -5.9335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.7726   -8.0642    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.5461   -8.7867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2941   -7.4862    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   19.1876   -7.3491    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.9278   -5.2221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.1913   -8.7757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8753   -6.7747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8827   -8.2013    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.0102   -7.3453    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0490   -6.7821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0565   -8.2124    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.2977   -8.9127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6413   -7.5047    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6265   -6.0706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6488   -8.9275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8188   -7.4936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0305   -5.3555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  1  6  0  0  0
  1  4  1  0  0  0  0
  2  5  1  0  0  0  0
  2  6  1  1  0  0  0
  7  3  1  6  0  0  0
  4  8  1  0  0  0  0
  4  9  1  1  0  0  0
  5 10  1  0  0  0  0
  6 11  1  0  0  0  0
  7 12  1  0  0  0  0
  7 13  1  0  0  0  0
  8 14  1  6  0  0  0
 10 15  1  6  0  0  0
 12 16  1  0  0  0  0
 12 17  1  6  0  0  0
 13 18  1  0  0  0  0
 19 15  1  6  0  0  0
 16 20  1  0  0  0  0
 16 21  1  1  0  0  0
 18 22  1  1  0  0  0
 19 23  1  0  0  0  0
 19 24  1  0  0  0  0
 20 25  1  6  0  0  0
 23 26  1  0  0  0  0
 23 27  1  1  0  0  0
 24 28  1  0  0  0  0
 24 29  1  1  0  0  0
 30 25  1  6  0  0  0
 26 31  1  0  0  0  0
 27 32  1  0  0  0  0
 28 33  1  6  0  0  0
 30 34  1  0  0  0  0
 30 35  1  0  0  0  0
 31 36  1  1  0  0  0
 34 37  2  0  0  0  0
 35 38  1  0  0  0  0
 35 39  1  6  0  0  0
 37 40  1  0  0  0  0
 37 41  1  0  0  0  0
 38 42  1  1  0  0  0
 40 43  1  1  0  0  0
 41 44  1  0  0  0  0
  8 10  1  0  0  0  0
 18 20  1  0  0  0  0
 28 31  1  0  0  0  0
 38 40  1  0  0  0  0
M  END

HMDB0014429
     RDKit          3D
Acarbose
 87 90  0  0  0  0  0  0  0  0999 V2000
   -2.7428   -1.7903    2.1266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1688   -0.4878    1.4901 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0329    0.2342    1.1971 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2196   -0.3885    0.2533 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0618    0.3230    0.0058 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0987   -0.3510    0.2518 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9113    0.4510    1.2701 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0623   -0.4165    2.5029 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7164    0.2623    3.5304 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1120    0.8686    0.7584 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0002   -0.1031    0.4508 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1187    0.3992   -0.2148 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2966   -0.0348    0.2987 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1911    1.0907    0.7246 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4093    2.1409    1.4491 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4713    2.6814    0.5753 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1934    0.5950    1.5870 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6968   -0.6091    1.0994 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0706   -1.6397    1.7860 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5154   -0.8177   -0.3639 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.1576    0.1267   -1.1550 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0453   -0.9534   -0.6824 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7049   -2.2877   -0.4720 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3329   -1.0607   -0.5217 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0734   -1.2119   -1.6916 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9717   -0.5120   -0.9736 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4675   -1.4656   -1.8570 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9751   -0.4588   -1.0536 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3354    0.2492   -2.0715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4201   -0.0204   -0.9027 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0527   -0.4122   -2.1032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9762   -0.7810    0.2637 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3766   -0.6930    0.4451 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9332    0.5500    0.8248 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7596    1.6612   -0.1484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4557    1.5872   -1.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3579    2.6353   -2.3019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9077    2.1390   -3.5210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3452    0.4201   -1.4687 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.1383    0.5508   -2.6056 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2183    0.3321   -0.2365 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.1395    1.3952   -0.3153 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4415    0.3835    1.0298 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.6149   -0.8238    1.7247 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7015   -1.7395    2.5268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4283   -2.0797    2.9479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7267   -2.6043    1.3711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7467    0.0560    2.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0553   -1.4029    0.6119 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8880   -1.3742    0.6187 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3616    1.3618    1.5959 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0671   -0.7114    2.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6427   -1.3378    2.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6828    0.1052    3.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3749   -0.7339    1.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0457   -0.6436    1.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6636    1.6060   -0.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8486    1.7408    2.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0794    2.9798    1.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7874    2.6400   -0.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7869   -0.6945    1.3560 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9990   -1.4820    2.7607 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0426   -1.7908   -0.6018 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1290   -0.0447   -1.1579 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8901   -0.6508   -1.7241 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2865   -2.3292    0.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1345   -2.0304   -0.0640 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1374   -2.1777   -1.8954 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0932    0.4600   -1.5070 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5889   -1.7536   -1.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9876   -1.5139   -1.3870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8256    1.0177   -1.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4102    1.0605   -0.8141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9704    0.3516   -2.7358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7768   -1.8724    0.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8782   -1.5399    0.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5692    0.9248    1.8136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0823    2.5073    0.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3438    3.1203   -2.5122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6825    3.4545   -1.9801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8911    2.9007   -4.1548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7457   -0.5284   -1.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5986    0.5216   -3.4308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7877   -0.6214   -0.3158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9645    1.1890    0.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8554    1.1786    1.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4453   -1.2769    1.4578 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 11 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
  4 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 37 38  1  0
 36 39  1  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 41 43  1  0
 43 44  1  0
 32  2  1  0
 43 34  1  0
 26  6  1  0
 22 13  1  0
  1 45  1  0
  1 46  1  0
  1 47  1  0
  2 48  1  1
  4 49  1  1
  6 50  1  1
  7 51  1  1
  8 52  1  0
  8 53  1  0
  9 54  1  0
 11 55  1  1
 13 56  1  1
 14 57  1  6
 15 58  1  0
 15 59  1  0
 16 60  1  0
 18 61  1  6
 19 62  1  0
 20 63  1  6
 21 64  1  0
 22 65  1  6
 23 66  1  0
 24 67  1  1
 25 68  1  0
 26 69  1  6
 27 70  1  0
 28 71  1  6
 29 72  1  0
 30 73  1  1
 31 74  1  0
 32 75  1  6
 33 76  1  0
 34 77  1  1
 35 78  1  0
 37 79  1  0
 37 80  1  0
 38 81  1  0
 39 82  1  6
 40 83  1  0
 41 84  1  6
 42 85  1  0
 43 86  1  1
 44 87  1  0
M  END

ChEBI
  Mrv0541 02231214342D          

 44 47  0  0  1  0            999 V2000
   14.2149   -7.4046    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.6151   -6.6931    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.3515   -7.4157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.6299   -8.1123    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.4414   -6.6857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.1926   -5.9818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5289   -7.4231    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.4525   -8.1087    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.2223   -8.8312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8638   -7.3935    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.6076   -5.2629    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1176   -8.1383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.1064   -6.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8675   -8.8164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.6864   -7.3824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2949   -8.1458    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.5326   -8.8497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2801   -6.7228    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.5349   -7.3639    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.8799   -7.4379    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.8873   -8.8683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8577   -6.0113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9426   -6.6488    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.9463   -8.0716    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.1166   -7.4788    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   18.7652   -6.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5201   -5.9335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.7726   -8.0642    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.5461   -8.7867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2941   -7.4862    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   19.1876   -7.3491    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.9278   -5.2221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.1913   -8.7757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8753   -6.7747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8827   -8.2013    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.0102   -7.3453    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0490   -6.7821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0565   -8.2124    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.2977   -8.9127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6413   -7.5047    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6265   -6.0706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6488   -8.9275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8188   -7.4936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0305   -5.3555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  1  6  0  0  0
  1  4  1  0  0  0  0
  2  5  1  0  0  0  0
  2  6  1  1  0  0  0
  7  3  1  6  0  0  0
  4  8  1  0  0  0  0
  4  9  1  1  0  0  0
  5 10  1  0  0  0  0
  6 11  1  0  0  0  0
  7 12  1  0  0  0  0
  7 13  1  0  0  0  0
  8 14  1  6  0  0  0
 10 15  1  6  0  0  0
 12 16  1  0  0  0  0
 12 17  1  6  0  0  0
 13 18  1  0  0  0  0
 19 15  1  6  0  0  0
 16 20  1  0  0  0  0
 16 21  1  1  0  0  0
 18 22  1  1  0  0  0
 19 23  1  0  0  0  0
 19 24  1  0  0  0  0
 20 25  1  6  0  0  0
 23 26  1  0  0  0  0
 23 27  1  1  0  0  0
 24 28  1  0  0  0  0
 24 29  1  1  0  0  0
 30 25  1  6  0  0  0
 26 31  1  0  0  0  0
 27 32  1  0  0  0  0
 28 33  1  6  0  0  0
 30 34  1  0  0  0  0
 30 35  1  0  0  0  0
 31 36  1  1  0  0  0
 34 37  2  0  0  0  0
 35 38  1  0  0  0  0
 35 39  1  6  0  0  0
 37 40  1  0  0  0  0
 37 41  1  0  0  0  0
 38 42  1  1  0  0  0
 40 43  1  1  0  0  0
 41 44  1  0  0  0  0
  8 10  1  0  0  0  0
 18 20  1  0  0  0  0
 28 31  1  0  0  0  0
 38 40  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0014429

> <DATABASE_NAME>
hmdb

> <SMILES>
C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H43NO18/c1-6-11(26-8-2-7(3-27)12(30)15(33)13(8)31)14(32)19(37)24(40-6)43-22-10(5-29)42-25(20(38)17(22)35)44-21-9(4-28)41-23(39)18(36)16(21)34/h2,6,8-39H,3-5H2,1H3/t6-,8+,9-,10-,11-,12+,13+,14+,15+,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-/m1/s1

> <INCHI_KEY>
XUFXOAAUWZOOIT-JMPDRRIHSA-N

> <FORMULA>
C25H43NO18

> <MOLECULAR_WEIGHT>
645.6048

> <EXACT_MASS>
645.248013577

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_AVERAGE_POLARIZABILITY>
62.3915134292925

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
14

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4R,5S,6R)-5-{[(2R,3R,4R,5S,6R)-5-{[(2R,3R,4S,5S,6R)-3,4-dihydroxy-6-methyl-5-{[(1S,4S,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)cyclohex-2-en-1-yl]amino}oxan-2-yl]oxy}-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-(hydroxymethyl)oxane-2,3,4-triol

> <ALOGPS_LOGP>
-2.66

> <JCHEM_LOGP>
-7.614558856666667

> <ALOGPS_LOGS>
-0.64

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.005879372132581

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.225573021156594

> <JCHEM_PKA_STRONGEST_BASIC>
7.031595061345334

> <JCHEM_POLAR_SURFACE_AREA>
321.17

> <JCHEM_REFRACTIVITY>
137.60240000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.48e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
acarbose

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0014429
     RDKit          3D
Acarbose
 87 90  0  0  0  0  0  0  0  0999 V2000
   -2.7428   -1.7903    2.1266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1688   -0.4878    1.4901 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0329    0.2342    1.1971 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2196   -0.3885    0.2533 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0618    0.3230    0.0058 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0987   -0.3510    0.2518 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9113    0.4510    1.2701 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0623   -0.4165    2.5029 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7164    0.2623    3.5304 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1120    0.8686    0.7584 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0002   -0.1031    0.4508 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1187    0.3992   -0.2148 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2966   -0.0348    0.2987 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1911    1.0907    0.7246 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4093    2.1409    1.4491 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4713    2.6814    0.5753 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1934    0.5950    1.5870 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6968   -0.6091    1.0994 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0706   -1.6397    1.7860 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5154   -0.8177   -0.3639 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.1576    0.1267   -1.1550 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0453   -0.9534   -0.6824 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7049   -2.2877   -0.4720 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3329   -1.0607   -0.5217 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0734   -1.2119   -1.6916 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9717   -0.5120   -0.9736 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4675   -1.4656   -1.8570 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9751   -0.4588   -1.0536 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3354    0.2492   -2.0715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4201   -0.0204   -0.9027 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0527   -0.4122   -2.1032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9762   -0.7810    0.2637 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3766   -0.6930    0.4451 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9332    0.5500    0.8248 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7596    1.6612   -0.1484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4557    1.5872   -1.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3579    2.6353   -2.3019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9077    2.1390   -3.5210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3452    0.4201   -1.4687 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.1383    0.5508   -2.6056 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2183    0.3321   -0.2365 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.1395    1.3952   -0.3153 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4415    0.3835    1.0298 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.6149   -0.8238    1.7247 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7015   -1.7395    2.5268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4283   -2.0797    2.9479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7267   -2.6043    1.3711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7467    0.0560    2.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0553   -1.4029    0.6119 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8880   -1.3742    0.6187 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3616    1.3618    1.5959 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0671   -0.7114    2.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6427   -1.3378    2.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6828    0.1052    3.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3749   -0.7339    1.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0457   -0.6436    1.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6636    1.6060   -0.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8486    1.7408    2.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0794    2.9798    1.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7874    2.6400   -0.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7869   -0.6945    1.3560 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9990   -1.4820    2.7607 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0426   -1.7908   -0.6018 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1290   -0.0447   -1.1579 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8901   -0.6508   -1.7241 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2865   -2.3292    0.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1345   -2.0304   -0.0640 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1374   -2.1777   -1.8954 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0932    0.4600   -1.5070 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5889   -1.7536   -1.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9876   -1.5139   -1.3870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8256    1.0177   -1.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4102    1.0605   -0.8141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9704    0.3516   -2.7358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7768   -1.8724    0.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8782   -1.5399    0.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5692    0.9248    1.8136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0823    2.5073    0.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3438    3.1203   -2.5122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6825    3.4545   -1.9801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8911    2.9007   -4.1548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7457   -0.5284   -1.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5986    0.5216   -3.4308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7877   -0.6214   -0.3158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9645    1.1890    0.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8554    1.1786    1.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4453   -1.2769    1.4578 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 11 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
  4 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 37 38  1  0
 36 39  1  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 41 43  1  0
 43 44  1  0
 32  2  1  0
 43 34  1  0
 26  6  1  0
 22 13  1  0
  1 45  1  0
  1 46  1  0
  1 47  1  0
  2 48  1  1
  4 49  1  1
  6 50  1  1
  7 51  1  1
  8 52  1  0
  8 53  1  0
  9 54  1  0
 11 55  1  1
 13 56  1  1
 14 57  1  6
 15 58  1  0
 15 59  1  0
 16 60  1  0
 18 61  1  6
 19 62  1  0
 20 63  1  6
 21 64  1  0
 22 65  1  6
 23 66  1  0
 24 67  1  1
 25 68  1  0
 26 69  1  6
 27 70  1  0
 28 71  1  6
 29 72  1  0
 30 73  1  1
 31 74  1  0
 32 75  1  6
 33 76  1  0
 34 77  1  1
 35 78  1  0
 37 79  1  0
 37 80  1  0
 38 81  1  0
 39 82  1  6
 40 83  1  0
 41 84  1  6
 42 85  1  0
 43 86  1  1
 44 87  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: ChEBI                                             
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0      26.534 -13.822   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      27.282 -12.494   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      24.923 -13.843   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      27.309 -15.143   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      28.824 -12.480   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      26.493 -11.166   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      23.387 -13.856   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      28.845 -15.136   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      26.548 -16.485   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      29.612 -13.801   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      27.268  -9.824   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      22.620 -15.191   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      22.599 -12.535   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      29.619 -16.457   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      31.148 -13.780   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      21.084 -15.205   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      23.394 -16.519   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      21.056 -12.549   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      32.732 -13.746   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      20.309 -13.884   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      20.323 -16.554   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      20.268 -11.221   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      33.493 -12.411   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      33.500 -15.067   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0      18.884 -13.960   0.000  0.00  0.00           N+0
HETATM   26  O   UNK     0      35.028 -12.404   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      32.704 -11.076   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      35.042 -15.053   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      32.753 -16.402   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      17.349 -13.974   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      35.817 -13.718   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      33.465  -9.748   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      35.824 -16.381   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      16.567 -12.646   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      16.581 -15.309   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      37.352 -13.711   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      15.025 -12.660   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      15.039 -15.330   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      17.356 -16.637   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      14.264 -14.009   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      14.236 -11.332   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      14.278 -16.665   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      12.728 -13.988   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0      14.990  -9.997   0.000  0.00  0.00           O+0
CONECT    1    2    3    4                                                  
CONECT    2    1    5    6                                                  
CONECT    3    1    7                                                       
CONECT    4    1    8    9                                                  
CONECT    5    2   10                                                       
CONECT    6    2   11                                                       
CONECT    7    3   12   13                                                  
CONECT    8    4   14   10                                                  
CONECT    9    4                                                            
CONECT   10    5   15    8                                                  
CONECT   11    6                                                            
CONECT   12    7   16   17                                                  
CONECT   13    7   18                                                       
CONECT   14    8                                                            
CONECT   15   10   19                                                       
CONECT   16   12   20   21                                                  
CONECT   17   12                                                            
CONECT   18   13   22   20                                                  
CONECT   19   15   23   24                                                  
CONECT   20   16   25   18                                                  
CONECT   21   16                                                            
CONECT   22   18                                                            
CONECT   23   19   26   27                                                  
CONECT   24   19   28   29                                                  
CONECT   25   20   30                                                       
CONECT   26   23   31                                                       
CONECT   27   23   32                                                       
CONECT   28   24   33   31                                                  
CONECT   29   24                                                            
CONECT   30   25   34   35                                                  
CONECT   31   26   36   28                                                  
CONECT   32   27                                                            
CONECT   33   28                                                            
CONECT   34   30   37                                                       
CONECT   35   30   38   39                                                  
CONECT   36   31                                                            
CONECT   37   34   40   41                                                  
CONECT   38   35   42   40                                                  
CONECT   39   35                                                            
CONECT   40   37   43   38                                                  
CONECT   41   37   44                                                       
CONECT   42   38                                                            
CONECT   43   40                                                            
CONECT   44   41                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   94    0
END

COMPND    HMDB0014429
HETATM    1  C1  UNL     1      -2.743  -1.790   2.127  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.169  -0.488   1.490  1.00  0.00           C  
HETATM    3  O1  UNL     1      -2.033   0.234   1.197  1.00  0.00           O  
HETATM    4  C3  UNL     1      -1.220  -0.389   0.253  1.00  0.00           C  
HETATM    5  O2  UNL     1      -0.062   0.323   0.006  1.00  0.00           O  
HETATM    6  C4  UNL     1       1.099  -0.351   0.252  1.00  0.00           C  
HETATM    7  C5  UNL     1       1.911   0.451   1.270  1.00  0.00           C  
HETATM    8  C6  UNL     1       2.062  -0.416   2.503  1.00  0.00           C  
HETATM    9  O3  UNL     1       2.716   0.262   3.530  1.00  0.00           O  
HETATM   10  O4  UNL     1       3.112   0.869   0.758  1.00  0.00           O  
HETATM   11  C7  UNL     1       4.000  -0.103   0.451  1.00  0.00           C  
HETATM   12  O5  UNL     1       5.119   0.399  -0.215  1.00  0.00           O  
HETATM   13  C8  UNL     1       6.297  -0.035   0.299  1.00  0.00           C  
HETATM   14  C9  UNL     1       7.191   1.091   0.725  1.00  0.00           C  
HETATM   15  C10 UNL     1       6.409   2.141   1.449  1.00  0.00           C  
HETATM   16  O6  UNL     1       5.471   2.681   0.575  1.00  0.00           O  
HETATM   17  O7  UNL     1       8.193   0.595   1.587  1.00  0.00           O  
HETATM   18  C11 UNL     1       8.697  -0.609   1.099  1.00  0.00           C  
HETATM   19  O8  UNL     1       8.071  -1.640   1.786  1.00  0.00           O  
HETATM   20  C12 UNL     1       8.515  -0.818  -0.364  1.00  0.00           C  
HETATM   21  O9  UNL     1       9.158   0.127  -1.155  1.00  0.00           O  
HETATM   22  C13 UNL     1       7.045  -0.953  -0.682  1.00  0.00           C  
HETATM   23  O10 UNL     1       6.705  -2.288  -0.472  1.00  0.00           O  
HETATM   24  C14 UNL     1       3.333  -1.061  -0.522  1.00  0.00           C  
HETATM   25  O11 UNL     1       4.073  -1.212  -1.692  1.00  0.00           O  
HETATM   26  C15 UNL     1       1.972  -0.512  -0.974  1.00  0.00           C  
HETATM   27  O12 UNL     1       1.467  -1.466  -1.857  1.00  0.00           O  
HETATM   28  C16 UNL     1      -1.975  -0.459  -1.054  1.00  0.00           C  
HETATM   29  O13 UNL     1      -1.335   0.249  -2.071  1.00  0.00           O  
HETATM   30  C17 UNL     1      -3.420  -0.020  -0.903  1.00  0.00           C  
HETATM   31  O14 UNL     1      -4.053  -0.412  -2.103  1.00  0.00           O  
HETATM   32  C18 UNL     1      -3.976  -0.781   0.264  1.00  0.00           C  
HETATM   33  N1  UNL     1      -5.377  -0.693   0.445  1.00  0.00           N  
HETATM   34  C19 UNL     1      -5.933   0.550   0.825  1.00  0.00           C  
HETATM   35  C20 UNL     1      -5.760   1.661  -0.148  1.00  0.00           C  
HETATM   36  C21 UNL     1      -6.456   1.587  -1.269  1.00  0.00           C  
HETATM   37  C22 UNL     1      -6.358   2.635  -2.302  1.00  0.00           C  
HETATM   38  O15 UNL     1      -5.908   2.139  -3.521  1.00  0.00           O  
HETATM   39  C23 UNL     1      -7.345   0.420  -1.469  1.00  0.00           C  
HETATM   40  O16 UNL     1      -8.138   0.551  -2.606  1.00  0.00           O  
HETATM   41  C24 UNL     1      -8.218   0.332  -0.237  1.00  0.00           C  
HETATM   42  O17 UNL     1      -9.140   1.395  -0.315  1.00  0.00           O  
HETATM   43  C25 UNL     1      -7.441   0.383   1.030  1.00  0.00           C  
HETATM   44  O18 UNL     1      -7.615  -0.824   1.725  1.00  0.00           O  
HETATM   45  H1  UNL     1      -1.701  -1.739   2.527  1.00  0.00           H  
HETATM   46  H2  UNL     1      -3.428  -2.080   2.948  1.00  0.00           H  
HETATM   47  H3  UNL     1      -2.727  -2.604   1.371  1.00  0.00           H  
HETATM   48  H4  UNL     1      -3.747   0.056   2.269  1.00  0.00           H  
HETATM   49  H5  UNL     1      -1.055  -1.403   0.612  1.00  0.00           H  
HETATM   50  H6  UNL     1       0.888  -1.374   0.619  1.00  0.00           H  
HETATM   51  H7  UNL     1       1.362   1.362   1.596  1.00  0.00           H  
HETATM   52  H8  UNL     1       1.067  -0.711   2.888  1.00  0.00           H  
HETATM   53  H9  UNL     1       2.643  -1.338   2.314  1.00  0.00           H  
HETATM   54  H10 UNL     1       3.683   0.105   3.485  1.00  0.00           H  
HETATM   55  H11 UNL     1       4.375  -0.734   1.274  1.00  0.00           H  
HETATM   56  H12 UNL     1       6.046  -0.644   1.217  1.00  0.00           H  
HETATM   57  H13 UNL     1       7.664   1.606  -0.156  1.00  0.00           H  
HETATM   58  H14 UNL     1       5.849   1.741   2.320  1.00  0.00           H  
HETATM   59  H15 UNL     1       7.079   2.980   1.739  1.00  0.00           H  
HETATM   60  H16 UNL     1       5.787   2.640  -0.383  1.00  0.00           H  
HETATM   61  H17 UNL     1       9.787  -0.695   1.356  1.00  0.00           H  
HETATM   62  H18 UNL     1       7.999  -1.482   2.761  1.00  0.00           H  
HETATM   63  H19 UNL     1       9.043  -1.791  -0.602  1.00  0.00           H  
HETATM   64  H20 UNL     1      10.129  -0.045  -1.158  1.00  0.00           H  
HETATM   65  H21 UNL     1       6.890  -0.651  -1.724  1.00  0.00           H  
HETATM   66  H22 UNL     1       6.286  -2.329   0.440  1.00  0.00           H  
HETATM   67  H23 UNL     1       3.135  -2.030  -0.064  1.00  0.00           H  
HETATM   68  H24 UNL     1       4.137  -2.178  -1.895  1.00  0.00           H  
HETATM   69  H25 UNL     1       2.093   0.460  -1.507  1.00  0.00           H  
HETATM   70  H26 UNL     1       0.589  -1.754  -1.500  1.00  0.00           H  
HETATM   71  H27 UNL     1      -1.988  -1.514  -1.387  1.00  0.00           H  
HETATM   72  H28 UNL     1      -0.826   1.018  -1.661  1.00  0.00           H  
HETATM   73  H29 UNL     1      -3.410   1.061  -0.814  1.00  0.00           H  
HETATM   74  H30 UNL     1      -3.970   0.352  -2.736  1.00  0.00           H  
HETATM   75  H31 UNL     1      -3.777  -1.872   0.004  1.00  0.00           H  
HETATM   76  H32 UNL     1      -5.878  -1.540   0.715  1.00  0.00           H  
HETATM   77  H33 UNL     1      -5.569   0.925   1.814  1.00  0.00           H  
HETATM   78  H34 UNL     1      -5.082   2.507   0.065  1.00  0.00           H  
HETATM   79  H35 UNL     1      -7.344   3.120  -2.512  1.00  0.00           H  
HETATM   80  H36 UNL     1      -5.682   3.455  -1.980  1.00  0.00           H  
HETATM   81  H37 UNL     1      -5.891   2.901  -4.155  1.00  0.00           H  
HETATM   82  H38 UNL     1      -6.746  -0.528  -1.546  1.00  0.00           H  
HETATM   83  H39 UNL     1      -7.599   0.522  -3.431  1.00  0.00           H  
HETATM   84  H40 UNL     1      -8.788  -0.621  -0.316  1.00  0.00           H  
HETATM   85  H41 UNL     1      -9.964   1.189   0.170  1.00  0.00           H  
HETATM   86  H42 UNL     1      -7.855   1.179   1.679  1.00  0.00           H  
HETATM   87  H43 UNL     1      -8.445  -1.277   1.458  1.00  0.00           H  
CONECT    1    2   45   46   47
CONECT    2    3   32   48
CONECT    3    4
CONECT    4    5   28   49
CONECT    5    6
CONECT    6    7   26   50
CONECT    7    8   10   51
CONECT    8    9   52   53
CONECT    9   54
CONECT   10   11
CONECT   11   12   24   55
CONECT   12   13
CONECT   13   14   22   56
CONECT   14   15   17   57
CONECT   15   16   58   59
CONECT   16   60
CONECT   17   18
CONECT   18   19   20   61
CONECT   19   62
CONECT   20   21   22   63
CONECT   21   64
CONECT   22   23   65
CONECT   23   66
CONECT   24   25   26   67
CONECT   25   68
CONECT   26   27   69
CONECT   27   70
CONECT   28   29   30   71
CONECT   29   72
CONECT   30   31   32   73
CONECT   31   74
CONECT   32   33   75
CONECT   33   34   76
CONECT   34   35   43   77
CONECT   35   36   36   78
CONECT   36   37   39
CONECT   37   38   79   80
CONECT   38   81
CONECT   39   40   41   82
CONECT   40   83
CONECT   41   42   43   84
CONECT   42   85
CONECT   43   44   86
CONECT   44   87
END

HMDB0014429
     RDKit          3D
Acarbose
 87 90  0  0  0  0  0  0  0  0999 V2000
   -2.7428   -1.7903    2.1266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1688   -0.4878    1.4901 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0329    0.2342    1.1971 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2196   -0.3885    0.2533 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0618    0.3230    0.0058 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0987   -0.3510    0.2518 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9113    0.4510    1.2701 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0623   -0.4165    2.5029 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7164    0.2623    3.5304 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1120    0.8686    0.7584 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0002   -0.1031    0.4508 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1187    0.3992   -0.2148 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2966   -0.0348    0.2987 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1911    1.0907    0.7246 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4093    2.1409    1.4491 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4713    2.6814    0.5753 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1934    0.5950    1.5870 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6968   -0.6091    1.0994 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0706   -1.6397    1.7860 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5154   -0.8177   -0.3639 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.1576    0.1267   -1.1550 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0453   -0.9534   -0.6824 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7049   -2.2877   -0.4720 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3329   -1.0607   -0.5217 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0734   -1.2119   -1.6916 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9717   -0.5120   -0.9736 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4675   -1.4656   -1.8570 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9751   -0.4588   -1.0536 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3354    0.2492   -2.0715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4201   -0.0204   -0.9027 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0527   -0.4122   -2.1032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9762   -0.7810    0.2637 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3766   -0.6930    0.4451 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9332    0.5500    0.8248 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7596    1.6612   -0.1484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4557    1.5872   -1.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3579    2.6353   -2.3019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9077    2.1390   -3.5210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3452    0.4201   -1.4687 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.1383    0.5508   -2.6056 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2183    0.3321   -0.2365 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.1395    1.3952   -0.3153 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4415    0.3835    1.0298 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.6149   -0.8238    1.7247 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7015   -1.7395    2.5268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4283   -2.0797    2.9479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7267   -2.6043    1.3711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7467    0.0560    2.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0553   -1.4029    0.6119 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8880   -1.3742    0.6187 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3616    1.3618    1.5959 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0671   -0.7114    2.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6427   -1.3378    2.3142 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6828    0.1052    3.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3749   -0.7339    1.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0457   -0.6436    1.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6636    1.6060   -0.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8486    1.7408    2.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0794    2.9798    1.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7874    2.6400   -0.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7869   -0.6945    1.3560 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9990   -1.4820    2.7607 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0426   -1.7908   -0.6018 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1290   -0.0447   -1.1579 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8901   -0.6508   -1.7241 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2865   -2.3292    0.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1345   -2.0304   -0.0640 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1374   -2.1777   -1.8954 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0932    0.4600   -1.5070 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5889   -1.7536   -1.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9876   -1.5139   -1.3870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8256    1.0177   -1.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4102    1.0605   -0.8141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9704    0.3516   -2.7358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7768   -1.8724    0.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8782   -1.5399    0.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5692    0.9248    1.8136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0823    2.5073    0.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3438    3.1203   -2.5122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6825    3.4545   -1.9801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8911    2.9007   -4.1548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7457   -0.5284   -1.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5986    0.5216   -3.4308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7877   -0.6214   -0.3158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9645    1.1890    0.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8554    1.1786    1.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4453   -1.2769    1.4578 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 11 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
  4 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 37 38  1  0
 36 39  1  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 41 43  1  0
 43 44  1  0
 32  2  1  0
 43 34  1  0
 26  6  1  0
 22 13  1  0
  1 45  1  0
  1 46  1  0
  1 47  1  0
  2 48  1  1
  4 49  1  1
  6 50  1  1
  7 51  1  1
  8 52  1  0
  8 53  1  0
  9 54  1  0
 11 55  1  1
 13 56  1  1
 14 57  1  6
 15 58  1  0
 15 59  1  0
 16 60  1  0
 18 61  1  6
 19 62  1  0
 20 63  1  6
 21 64  1  0
 22 65  1  6
 23 66  1  0
 24 67  1  1
 25 68  1  0
 26 69  1  6
 27 70  1  0
 28 71  1  6
 29 72  1  0
 30 73  1  1
 31 74  1  0
 32 75  1  6
 33 76  1  0
 34 77  1  1
 35 78  1  0
 37 79  1  0
 37 80  1  0
 38 81  1  0
 39 82  1  6
 40 83  1  0
 41 84  1  6
 42 85  1  0
 43 86  1  1
 44 87  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Bay g 5421	HMDB
Glumida	HMDB
Lasa brand OF acarbose	HMDB
Precose	HMDB
Bayer brand OF acarbose	HMDB
Prandase	HMDB
Glucor	HMDB
Glucobay	HMDB
Acarbose	MeSH

Chemical Formula

C₂₅H₄₃NO₁₈

Average Molecular Weight

645.6048

Monoisotopic Molecular Weight

645.248013577

IUPAC Name

(2R,3R,4R,5S,6R)-5-{[(2R,3R,4R,5S,6R)-5-{[(2R,3R,4S,5S,6R)-3,4-dihydroxy-6-methyl-5-{[(1S,4S,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)cyclohex-2-en-1-yl]amino}oxan-2-yl]oxy}-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-(hydroxymethyl)oxane-2,3,4-triol

Traditional Name

acarbose

CAS Registry Number

56180-94-0

SMILES

C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C25H43NO18/c1-6-11(26-8-2-7(3-27)12(30)15(33)13(8)31)14(32)19(37)24(40-6)43-22-10(5-29)42-25(20(38)17(22)35)44-21-9(4-28)41-23(39)18(36)16(21)34/h2,6,8-39H,3-5H2,1H3/t6-,8+,9-,10-,11-,12+,13+,14+,15+,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-/m1/s1

InChI Key

XUFXOAAUWZOOIT-JMPDRRIHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aminocyclitol glycosides. These are organic compounds containing an amicocyclitol moiety glycosidically linked to a carbohydrate moiety. There are two major classes of aminoglycosides containing a 2-streptamine core. They are called 4,5- and 4,6-disubstituted 2-deoxystreptamines.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Aminocyclitol glycosides

Alternative Parents

Substituents

Oligosaccharide
Amino cyclitol glycoside
Glycosyl compound
O-glycosyl compound
Cyclitol or derivatives
Oxane
1,2-aminoalcohol
Hemiacetal
Secondary alcohol
Secondary amine
Organoheterocyclic compound
Acetal
Oxacycle
Secondary aliphatic amine
Polyol
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Amine
Primary alcohol
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	148 g/L	Not Available
LogP	-6.8	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	148 g/L	ALOGPS
logP	-2.7	ALOGPS
logP	-7.6	ChemAxon
logS	-0.64	ALOGPS
pKa (Strongest Acidic)	11.23	ChemAxon
pKa (Strongest Basic)	7.03	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	19	ChemAxon
Hydrogen Donor Count	14	ChemAxon
Polar Surface Area	321.17 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	137.6 m³·mol⁻¹	ChemAxon
Polarizability	62.39 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	232.63	30932474
DeepCCS	[M-H]-	230.907	30932474
DeepCCS	[M-2H]-	265.041	30932474
DeepCCS	[M+Na]+	238.88	30932474
AllCCS	[M+H]+	239.0	32859911
AllCCS	[M+H-H2O]+	238.4	32859911
AllCCS	[M+NH4]+	239.5	32859911
AllCCS	[M+Na]+	239.6	32859911
AllCCS	[M-H]-	230.2	32859911
AllCCS	[M+Na-2H]-	231.7	32859911
AllCCS	[M+HCOO]-	233.4	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	1.5 minutes	32390414
Predicted by Siyang on May 30, 2022	12.743 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	9.02 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	550.4 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	633.8 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	257.7 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	23.1 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	216.8 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	107.7 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	445.1 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	333.8 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	1140.7 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	702.4 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	79.4 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	955.1 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	284.6 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	445.0 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	898.5 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	775.2 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	625.2 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Acarbose	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4186.0	Standard polar	33892256
Acarbose	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4742.1	Standard non polar	33892256
Acarbose	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5638.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Acarbose,1TMS,isomer #1	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4914.4	Semi standard non polar	33892256
Acarbose,1TMS,isomer #10	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4918.7	Semi standard non polar	33892256
Acarbose,1TMS,isomer #11	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4891.7	Semi standard non polar	33892256
Acarbose,1TMS,isomer #12	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4888.1	Semi standard non polar	33892256
Acarbose,1TMS,isomer #13	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4898.0	Semi standard non polar	33892256
Acarbose,1TMS,isomer #14	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4929.0	Semi standard non polar	33892256
Acarbose,1TMS,isomer #2	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4910.1	Semi standard non polar	33892256
Acarbose,1TMS,isomer #3	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4888.6	Semi standard non polar	33892256
Acarbose,1TMS,isomer #4	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4901.7	Semi standard non polar	33892256
Acarbose,1TMS,isomer #5	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4885.0	Semi standard non polar	33892256
Acarbose,1TMS,isomer #6	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4905.6	Semi standard non polar	33892256
Acarbose,1TMS,isomer #7	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4895.1	Semi standard non polar	33892256
Acarbose,1TMS,isomer #8	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4889.3	Semi standard non polar	33892256
Acarbose,1TMS,isomer #9	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4880.3	Semi standard non polar	33892256
Acarbose,2TMS,isomer #1	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4817.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #10	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4802.9	Semi standard non polar	33892256
Acarbose,2TMS,isomer #11	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4787.7	Semi standard non polar	33892256
Acarbose,2TMS,isomer #12	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4788.1	Semi standard non polar	33892256
Acarbose,2TMS,isomer #13	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4860.3	Semi standard non polar	33892256
Acarbose,2TMS,isomer #14	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4774.7	Semi standard non polar	33892256
Acarbose,2TMS,isomer #15	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4797.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #16	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4787.7	Semi standard non polar	33892256
Acarbose,2TMS,isomer #17	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4790.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #18	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4782.8	Semi standard non polar	33892256
Acarbose,2TMS,isomer #19	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4785.0	Semi standard non polar	33892256
Acarbose,2TMS,isomer #2	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4784.5	Semi standard non polar	33892256
Acarbose,2TMS,isomer #20	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4776.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #21	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4817.9	Semi standard non polar	33892256
Acarbose,2TMS,isomer #22	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4800.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #23	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4786.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #24	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4785.7	Semi standard non polar	33892256
Acarbose,2TMS,isomer #25	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4860.3	Semi standard non polar	33892256
Acarbose,2TMS,isomer #26	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4786.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #27	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4765.0	Semi standard non polar	33892256
Acarbose,2TMS,isomer #28	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4770.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #29	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4763.1	Semi standard non polar	33892256
Acarbose,2TMS,isomer #3	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4793.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #30	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4766.1	Semi standard non polar	33892256
Acarbose,2TMS,isomer #31	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4760.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #32	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4796.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #33	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4787.5	Semi standard non polar	33892256
Acarbose,2TMS,isomer #34	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4779.0	Semi standard non polar	33892256
Acarbose,2TMS,isomer #35	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4771.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #36	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4838.1	Semi standard non polar	33892256
Acarbose,2TMS,isomer #37	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4790.6	Semi standard non polar	33892256
Acarbose,2TMS,isomer #38	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4776.1	Semi standard non polar	33892256
Acarbose,2TMS,isomer #39	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4769.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #4	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4784.6	Semi standard non polar	33892256
Acarbose,2TMS,isomer #40	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4770.1	Semi standard non polar	33892256
Acarbose,2TMS,isomer #41	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4763.1	Semi standard non polar	33892256
Acarbose,2TMS,isomer #42	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4805.8	Semi standard non polar	33892256
Acarbose,2TMS,isomer #43	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4792.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #44	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4781.9	Semi standard non polar	33892256
Acarbose,2TMS,isomer #45	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4773.1	Semi standard non polar	33892256
Acarbose,2TMS,isomer #46	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4850.1	Semi standard non polar	33892256
Acarbose,2TMS,isomer #47	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4770.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #48	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4764.5	Semi standard non polar	33892256
Acarbose,2TMS,isomer #49	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4765.6	Semi standard non polar	33892256
Acarbose,2TMS,isomer #5	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4797.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #50	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4757.7	Semi standard non polar	33892256
Acarbose,2TMS,isomer #51	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4798.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #52	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4785.5	Semi standard non polar	33892256
Acarbose,2TMS,isomer #53	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4773.6	Semi standard non polar	33892256
Acarbose,2TMS,isomer #54	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4769.6	Semi standard non polar	33892256
Acarbose,2TMS,isomer #55	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4833.8	Semi standard non polar	33892256
Acarbose,2TMS,isomer #56	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4790.6	Semi standard non polar	33892256
Acarbose,2TMS,isomer #57	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4770.0	Semi standard non polar	33892256
Acarbose,2TMS,isomer #58	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4760.0	Semi standard non polar	33892256
Acarbose,2TMS,isomer #59	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4804.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #6	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4787.5	Semi standard non polar	33892256
Acarbose,2TMS,isomer #60	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4791.6	Semi standard non polar	33892256
Acarbose,2TMS,isomer #61	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4773.5	Semi standard non polar	33892256
Acarbose,2TMS,isomer #62	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4770.3	Semi standard non polar	33892256
Acarbose,2TMS,isomer #63	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4847.3	Semi standard non polar	33892256
Acarbose,2TMS,isomer #64	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4761.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #65	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4751.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #66	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4795.6	Semi standard non polar	33892256
Acarbose,2TMS,isomer #67	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4783.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #68	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4765.6	Semi standard non polar	33892256
Acarbose,2TMS,isomer #69	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4762.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #7	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4789.0	Semi standard non polar	33892256
Acarbose,2TMS,isomer #70	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4841.2	Semi standard non polar	33892256
Acarbose,2TMS,isomer #71	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4773.1	Semi standard non polar	33892256
Acarbose,2TMS,isomer #72	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4798.3	Semi standard non polar	33892256
Acarbose,2TMS,isomer #73	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4783.8	Semi standard non polar	33892256
Acarbose,2TMS,isomer #74	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4764.8	Semi standard non polar	33892256
Acarbose,2TMS,isomer #75	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4767.3	Semi standard non polar	33892256
Acarbose,2TMS,isomer #76	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4836.8	Semi standard non polar	33892256
Acarbose,2TMS,isomer #77	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4791.7	Semi standard non polar	33892256
Acarbose,2TMS,isomer #78	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4775.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #79	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4756.3	Semi standard non polar	33892256
Acarbose,2TMS,isomer #8	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4780.6	Semi standard non polar	33892256
Acarbose,2TMS,isomer #80	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4760.5	Semi standard non polar	33892256
Acarbose,2TMS,isomer #81	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4826.1	Semi standard non polar	33892256
Acarbose,2TMS,isomer #82	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4815.9	Semi standard non polar	33892256
Acarbose,2TMS,isomer #83	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4798.5	Semi standard non polar	33892256
Acarbose,2TMS,isomer #84	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4808.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #85	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4858.3	Semi standard non polar	33892256
Acarbose,2TMS,isomer #86	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4793.9	Semi standard non polar	33892256
Acarbose,2TMS,isomer #87	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4782.4	Semi standard non polar	33892256
Acarbose,2TMS,isomer #88	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	4844.1	Semi standard non polar	33892256
Acarbose,2TMS,isomer #89	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4778.5	Semi standard non polar	33892256
Acarbose,2TMS,isomer #9	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4819.8	Semi standard non polar	33892256
Acarbose,2TMS,isomer #90	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	4835.6	Semi standard non polar	33892256
Acarbose,2TMS,isomer #91	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4835.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #1	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4561.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #10	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4574.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #100	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4556.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #101	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4562.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #102	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4566.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #103	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4558.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #104	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4625.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #105	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4595.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #106	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4564.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #107	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4551.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #108	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4743.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #109	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4591.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #11	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4564.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #110	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4561.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #111	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4551.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #112	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4617.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #113	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4587.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #114	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4557.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #115	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4542.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #116	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4739.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #117	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4558.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #118	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4552.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #119	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4617.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #12	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4778.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #120	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4589.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #121	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4559.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #122	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4542.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #123	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4736.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #124	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4583.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #125	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4627.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #126	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4596.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #127	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4562.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #128	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4551.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #129	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4731.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #13	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4574.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #130	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4612.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #131	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4581.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #132	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4553.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #133	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4541.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #134	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4724.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #135	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4663.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #136	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4620.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #137	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4624.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #138	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4798.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #139	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4600.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #14	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4558.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #140	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4575.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #141	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	4764.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #142	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4558.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #143	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	4744.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #144	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4728.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #145	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4607.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #146	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4566.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #147	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4566.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #148	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4568.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #149	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4566.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #15	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4565.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #150	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4628.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #151	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4608.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #152	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4577.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #153	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4559.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #154	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4725.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #155	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4552.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #156	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4553.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #157	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4555.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #158	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4553.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #159	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4613.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #16	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4553.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #160	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4595.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #161	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4561.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #162	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4549.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #163	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4708.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #164	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4583.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #165	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4551.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #166	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4549.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #167	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4612.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #168	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4591.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #169	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4557.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #17	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4567.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #170	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4545.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #171	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4714.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #172	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4550.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #173	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4549.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #174	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4612.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #175	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4594.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #176	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4560.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #177	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4547.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #178	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4711.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #179	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4576.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #18	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4561.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #180	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4621.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #181	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4598.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #182	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4562.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #183	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4549.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #184	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4704.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #185	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4609.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #186	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4588.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #187	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4555.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #188	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4546.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #189	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4702.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #19	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4623.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #190	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4664.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #191	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4624.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #192	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4628.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #193	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4780.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #194	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4610.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #195	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4585.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #196	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	4742.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #197	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4565.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #198	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	4722.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #199	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4708.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #2	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4592.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #20	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4599.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #200	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4576.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #201	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4577.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #202	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4578.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #203	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4577.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #204	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4635.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #205	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4611.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #206	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4582.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #207	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4569.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #208	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4727.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #209	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4586.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #21	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4567.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #210	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4551.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #211	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4549.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #212	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4607.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #213	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4585.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #214	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4555.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #215	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4542.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #216	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4710.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #217	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4555.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #218	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4553.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #219	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4608.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #22	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4550.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #220	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4590.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #221	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4560.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #222	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4548.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #223	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4711.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #224	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4579.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #225	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4616.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #226	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4592.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #227	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4560.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #228	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4551.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #229	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4701.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #23	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4741.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #230	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4605.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #231	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4584.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #232	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4559.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #233	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4549.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #234	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4696.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #235	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4650.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #236	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4615.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #237	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4621.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #238	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4777.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #239	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4602.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #24	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4585.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #240	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4580.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #241	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	4732.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #242	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4569.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #243	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	4715.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #244	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4701.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #245	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4586.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #246	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4552.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #247	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4549.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #248	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4612.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #249	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4586.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #25	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4567.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #250	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4554.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #251	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4542.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #252	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4711.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #253	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4554.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #254	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4553.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #255	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4615.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #256	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4593.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #257	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4560.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #258	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4549.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #259	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4708.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #26	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4559.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #260	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4576.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #261	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4624.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #262	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4597.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #263	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4560.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #264	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4552.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #265	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4703.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #266	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4610.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #267	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4585.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #268	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4556.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #269	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4548.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #27	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4564.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #270	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4699.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #271	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4662.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #272	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4621.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #273	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4623.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #274	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4777.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #275	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4608.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #276	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4584.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #277	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	4736.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #278	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4567.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #279	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	4716.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #28	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4561.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #280	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4704.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #281	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4579.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #282	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4575.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #283	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4636.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #284	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4613.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #285	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4585.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #286	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4567.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #287	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4726.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #288	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4568.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #289	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4609.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #29	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4624.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #290	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4580.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #291	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4547.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #292	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4540.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #293	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4699.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #294	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4594.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #295	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4570.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #296	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4542.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #297	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4533.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #298	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4694.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #299	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4644.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #3	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4581.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #30	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4593.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #300	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4603.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #301	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4606.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #302	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4776.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #303	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4588.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #304	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4567.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #305	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	4727.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #306	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4554.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #307	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	4709.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #308	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4697.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #309	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4566.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #31	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4565.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #310	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4609.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #311	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4582.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #312	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4547.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #313	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4538.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #314	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4699.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #315	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4595.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #316	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4575.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #317	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4546.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #318	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4538.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #319	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4691.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #32	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4553.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #320	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4647.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #321	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4605.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #322	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4607.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #323	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4772.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #324	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4595.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #325	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4571.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #326	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	4727.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #327	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4557.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #328	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	4706.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #329	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4696.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #33	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4738.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #330	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4630.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #331	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4599.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #332	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4567.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #333	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4559.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #334	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4704.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #335	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4651.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #336	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4612.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #337	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4614.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #338	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4768.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #339	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4595.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #34	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4567.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #340	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4571.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #341	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	4719.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #342	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4557.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #343	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	4702.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #344	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4689.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #345	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4639.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #346	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4599.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #347	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4606.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #348	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4762.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #349	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4584.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #35	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4560.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #350	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4567.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #351	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	4716.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #352	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4552.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #353	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	4694.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #354	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4679.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #355	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4664.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #356	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4642.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #357	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	4800.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #358	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4612.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #359	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	4775.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #36	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4570.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #360	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4768.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #361	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4596.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #362	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	4735.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #363	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4722.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #364	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4706.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #37	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4563.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #38	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4630.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #39	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4600.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #4	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4587.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #40	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4569.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #41	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4553.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #42	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4743.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #43	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4597.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #44	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4570.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #45	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4559.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #46	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4628.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #47	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4596.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #48	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4565.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #49	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4550.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #5	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4574.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #50	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4742.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #51	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4555.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #52	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4549.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #53	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4611.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #54	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4582.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #55	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4552.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #56	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4540.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #57	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4737.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #58	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4586.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #59	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4628.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #6	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4585.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #60	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4597.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #61	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4563.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #62	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4552.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #63	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4731.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #64	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4614.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #65	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4585.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #66	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4556.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #67	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4544.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #68	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4722.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #69	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4663.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #7	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4577.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #70	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4619.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #71	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4624.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #72	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4798.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #73	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4601.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #74	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4578.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #75	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	4764.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #76	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4560.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #77	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	4743.4	Semi standard non polar	33892256
Acarbose,3TMS,isomer #78	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	4726.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #79	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)O[C@@H]3CO[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4558.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #8	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4644.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #80	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4541.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #81	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4545.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #82	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4545.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #83	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4552.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #84	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4546.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #85	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4611.2	Semi standard non polar	33892256
Acarbose,3TMS,isomer #86	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4586.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #87	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4555.0	Semi standard non polar	33892256
Acarbose,3TMS,isomer #88	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4538.7	Semi standard non polar	33892256
Acarbose,3TMS,isomer #89	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4730.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #9	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4603.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #90	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4590.3	Semi standard non polar	33892256
Acarbose,3TMS,isomer #91	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4567.8	Semi standard non polar	33892256
Acarbose,3TMS,isomer #92	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4568.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #93	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4572.1	Semi standard non polar	33892256
Acarbose,3TMS,isomer #94	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	4566.6	Semi standard non polar	33892256
Acarbose,3TMS,isomer #95	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4634.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #96	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4602.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #97	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4574.9	Semi standard non polar	33892256
Acarbose,3TMS,isomer #98	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4561.5	Semi standard non polar	33892256
Acarbose,3TMS,isomer #99	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	4744.0	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #1	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5064.1	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #10	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5097.8	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #11	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5074.6	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #12	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5068.5	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #13	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5070.7	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #14	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	5130.7	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #2	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5061.5	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #3	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5042.8	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #4	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5065.8	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #5	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5051.5	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #6	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5065.9	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #7	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5061.0	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #8	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5052.5	Semi standard non polar	33892256
Acarbose,1TBDMS,isomer #9	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5055.6	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #1	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5097.8	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #10	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5111.2	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #11	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5090.7	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #12	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5083.8	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #13	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	5198.8	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #14	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5051.2	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #15	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5092.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #16	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5077.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #17	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5074.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #18	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5080.6	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #19	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5075.8	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #2	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5066.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #20	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5083.3	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #21	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5132.1	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #22	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5109.1	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #23	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5089.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #24	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5080.0	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #25	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	5196.0	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #26	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5066.6	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #27	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5053.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #28	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5055.7	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #29	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5057.6	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #3	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5090.6	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #30	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5053.9	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #31	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5063.5	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #32	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5103.0	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #33	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5093.0	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #34	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5074.8	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #35	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5063.3	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #36	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	5174.9	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #37	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5084.2	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #38	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5072.5	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #39	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5076.6	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #4	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5082.7	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #40	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5073.3	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #41	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5079.2	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #42	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5119.9	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #43	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5105.7	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #44	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5089.5	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #45	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5080.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #46	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)O[C@@H]3CO)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	5189.0	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #47	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5060.5	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #48	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5068.6	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #49	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5065.0	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #5	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5080.7	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #50	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5071.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #51	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5114.8	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #52	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5098.9	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #53	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5080.0	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #54	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5070.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #55	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	5177.9	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #56	C[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5086.8	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #57	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5062.2	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #58	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5066.3	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #59	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5107.8	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #6	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5080.2	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #60	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5093.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #61	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5074.1	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #62	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5066.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #63	C[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	5186.9	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #64	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5060.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #65	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5069.1	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #66	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5111.2	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #67	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5097.8	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #68	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5076.5	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #69	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5069.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #7	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5079.0	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #70	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	5182.9	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #71	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5082.2	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #72	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5107.6	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #73	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5095.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #74	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5071.5	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #75	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5067.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #76	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	5181.3	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #77	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5111.7	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #78	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5100.0	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #79	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5075.9	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #8	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O	5085.7	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #80	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5073.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #81	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	5177.8	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #82	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5136.1	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #83	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5112.9	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #84	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5124.0	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #85	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	5205.8	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #86	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5091.8	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #87	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5086.4	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #88	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	5200.6	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #89	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	5072.0	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #9	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5133.0	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #90	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	5191.7	Semi standard non polar	33892256
Acarbose,2TBDMS,isomer #91	C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N([C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5181.6	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_11) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_12) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_13) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_1_14) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Acarbose GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental LC-MS/MS	LC-MS/MS Spectrum - Acarbose 40V, Positive-QTOF	splash10-0002-3902000000-3fb018175798c9231239	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Acarbose 20V, Negative-QTOF	splash10-03k9-1947240000-4b6ee2c3a91255b06d12	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Acarbose 10V, Negative-QTOF	splash10-0229-0528971000-1af97e1b697165e4682a	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Acarbose 40V, Negative-QTOF	splash10-0hn0-8952000000-da9ae13453070c132d04	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Acarbose 40V, Positive-QTOF	splash10-0002-3902000000-44bb8cb036eb4a8ff078	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Acarbose 20V, Positive-QTOF	splash10-0udj-0109003000-32ed472fac125e9c0138	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Acarbose 10V, Positive-QTOF	splash10-0002-0002009000-cba8078fd9f0804ff57e	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Acarbose 10V, Positive-QTOF	splash10-0002-0001009000-9350edc710cb09a03433	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Acarbose 20V, Positive-QTOF	splash10-0udj-0109003000-2f99e405b1fe24dc10b9	2021-09-20	HMDB team, MONA	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Acarbose 10V, Positive-QTOF	splash10-01u0-0907008000-c4d00c74315ba7f05c71	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Acarbose 20V, Positive-QTOF	splash10-01si-0904001000-d4cd2cc4441bc3625d29	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Acarbose 40V, Positive-QTOF	splash10-01q9-0902000000-73d6e311ce87b6f6ea5e	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Acarbose 10V, Negative-QTOF	splash10-002f-0494236000-a0af07f992dc784cf4a5	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Acarbose 20V, Negative-QTOF	splash10-004i-2915114000-1ad6a7433fabad9f48fa	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Acarbose 40V, Negative-QTOF	splash10-003r-2952000000-d6682d61c53540179001	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Acarbose 10V, Positive-QTOF	splash10-0f6t-0204209000-7d57cc67074b07ccd03b	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Acarbose 20V, Positive-QTOF	splash10-0uka-0619303000-e56c980cc818f02a6709	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Acarbose 40V, Positive-QTOF	splash10-0002-0913000000-f1be4304e9aec6c82c90	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Acarbose 10V, Negative-QTOF	splash10-0006-0005029000-cd3b5270336317dd439f	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Acarbose 20V, Negative-QTOF	splash10-0udi-1109001000-8c4c7575578bfcb430f2	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Acarbose 40V, Negative-QTOF	splash10-0a4i-8911010000-02edaec0a99cada585e8	2021-09-25	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular
Membrane

Biospecimen Locations

Blood
Urine

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Available	Not Available	Taking drug identified by DrugBank entry DB00284	21059682	details
Urine	Expected but not Quantified	Not Quantified	Not Available	Not Available	Taking drug identified by DrugBank entry DB00284	21059682	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

389971

KEGG Compound ID

C06802

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Acarbose

METLIN ID

Not Available

PubChem Compound

441184

PDB ID

Not Available

ChEBI ID

2376

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Clissold SP, Edwards C: Acarbose. A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential. Drugs. 1988 Mar;35(3):214-43. [PubMed:3286212 ]
(). FDA label . .

Enzymes

Enzyme Details

1. Sucrase-isomaltase, intestinal

General function:: Involved in catalytic activity
Specific function:: Plays an important role in the final stage of carbohydrate digestion. Isomaltase activity is specific for both alpha-1,4- and alpha-1,6-oligosaccharides.
Gene Name:: SI
Uniprot ID:: P14410
Molecular weight:: Not Available

References

Juretic D, Bernik S, Cop L, Hadzija M, Petlevski R, Lukac-Bajalo J: Short-term effect of acarbose on specific intestinal disaccharidase activities and hyperglycaemia in CBA diabetic mice. J Anim Physiol Anim Nutr (Berl). 2003 Aug;87(7-8):263-8. [PubMed:12864906 ]
Meyer H, Wieczorek H, Zeiske W: K+ transport in the caterpillar intestine epithelium: role of osmolytes for the K+-secretory capacity of the tobacco hornworm midgut. J Comp Physiol B. 2004 Oct;174(7):527-39. Epub 2004 Aug 20. [PubMed:15322845 ]
Karley AJ, Ashford DA, Minto LM, Pritchard J, Douglas AE: The significance of gut sucrase activity for osmoregulation in the pea aphid, Acyrthosiphon pisum. J Insect Physiol. 2005 Dec;51(12):1313-9. Epub 2005 Sep 15. [PubMed:16169004 ]
Samulitis BK, Goda T, Lee SM, Koldovsky O: Inhibitory mechanism of acarbose and 1-deoxynojirimycin derivatives on carbohydrases in rat small intestine. Drugs Exp Clin Res. 1987;13(8):517-24. [PubMed:2962844 ]
Newbrun E, Hoover CI, Walker GJ: Inhibition by acarbose, nojirimycin and 1-deoxynojirimycin of glucosyltransferase produced by oral streptococci. Arch Oral Biol. 1983;28(6):531-6. [PubMed:6226260 ]

Enzyme Details

2. Lysosomal alpha-glucosidase

General function:: Involved in catalytic activity
Specific function:: Essential for the degradation of glygogen to glucose in lysosomes.
Gene Name:: GAA
Uniprot ID:: P10253
Molecular weight:: Not Available

References

Salehi A, Fan BG, Ekelund M, Nordin G, Lundquist I: TPN-evoked dysfunction of islet lysosomal activity mediates impairment of glucose-stimulated insulin release. Am J Physiol Endocrinol Metab. 2001 Jul;281(1):E171-9. [PubMed:11404235 ]
Li Y, Scott CR, Chamoles NA, Ghavami A, Pinto BM, Turecek F, Gelb MH: Direct multiplex assay of lysosomal enzymes in dried blood spots for newborn screening. Clin Chem. 2004 Oct;50(10):1785-96. Epub 2004 Aug 3. [PubMed:15292070 ]
Lundquist I, Panagiotidis G: The relationship of islet amyloglucosidase activity and glucose-induced insulin secretion. Pancreas. 1992;7(3):352-7. [PubMed:1594557 ]
Zhang H, Kallwass H, Young SP, Carr C, Dai J, Kishnani PS, Millington DS, Keutzer J, Chen YT, Bali D: Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease. Genet Med. 2006 May;8(5):302-6. [PubMed:16702880 ]
Gelb MH, Turecek F, Scott CR, Chamoles NA: Direct multiplex assay of enzymes in dried blood spots by tandem mass spectrometry for the newborn screening of lysosomal storage disorders. J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):397-404. [PubMed:16763908 ]
Lullmann-Rauch R, Watermann D: Fusion of storage lysosomes in experimental lipidosis and glycogenosis. Exp Mol Pathol. 1987 Feb;46(1):136-43. [PubMed:3467980 ]
Bourbon JR, Doucet E, Rieutort M: Role of alpha-glucosidase in fetal lung maturation. Biochim Biophys Acta. 1987 Jan 13;917(1):203-10. [PubMed:3539207 ]
Chen X, Ji ZL, Chen YZ: TTD: Therapeutic Target Database. Nucleic Acids Res. 2002 Jan 1;30(1):412-5. [PubMed:11752352 ]

Enzyme Details

3. Pancreatic alpha-amylase

General function:: Involved in catalytic activity
Specific function:: Not Available
Gene Name:: AMY2A
Uniprot ID:: P04746
Molecular weight:: Not Available

References

Jonas L, Mikkat U, Lehmann R, Schareck W, Walzel H, Schroder W, Lopp H, Pussa T, Toomik P: Inhibitory effects of human and porcine alpha-amylase on CCK-8-stimulated lipase secretion of isolated rat pancreatic acini. Pancreatology. 2003;3(4):342-8. [PubMed:12890998 ]

Enzyme Details

4. Maltase-glucoamylase, intestinal

General function:: Involved in catalytic activity
Specific function:: May serve as an alternate pathway for starch digestion when luminal alpha-amylase activity is reduced because of immaturity or malnutrition. May play a unique role in the digestion of malted dietary oligosaccharides used in food manufacturing.
Gene Name:: MGAM
Uniprot ID:: O43451
Molecular weight:: Not Available

References

Okumiya T, Keulemans JL, Kroos MA, Van der Beek NM, Boer MA, Takeuchi H, Van Diggelen OP, Reuser AJ: A new diagnostic assay for glycogen storage disease type II in mixed leukocytes. Mol Genet Metab. 2006 May;88(1):22-8. Epub 2005 Dec 15. [PubMed:16359900 ]
Zhang H, Kallwass H, Young SP, Carr C, Dai J, Kishnani PS, Millington DS, Keutzer J, Chen YT, Bali D: Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease. Genet Med. 2006 May;8(5):302-6. [PubMed:16702880 ]
Gelb MH, Turecek F, Scott CR, Chamoles NA: Direct multiplex assay of enzymes in dried blood spots by tandem mass spectrometry for the newborn screening of lysosomal storage disorders. J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):397-404. [PubMed:16763908 ]
Yamagishi S, Matsui T, Ueda S, Fukami K, Okuda S: Clinical utility of acarbose, an alpha-glucosidase inhibitor in cardiometabolic disorders. Curr Drug Metab. 2009 Feb;10(2):159-63. [PubMed:19275550 ]
Chen X, Ji ZL, Chen YZ: TTD: Therapeutic Target Database. Nucleic Acids Res. 2002 Jan 1;30(1):412-5. [PubMed:11752352 ]

Showing metabocard for Acarbose (HMDB0014429)

MOL for HMDB0014429 (Acarbose)

3D MOL for HMDB0014429 (Acarbose)

3D SDF for HMDB0014429 (Acarbose)

3D-SDF for HMDB0014429 (Acarbose)

PDB for HMDB0014429 (Acarbose)

3D PDB for HMDB0014429 (Acarbose)

SMILES for HMDB0014429 (Acarbose)

INCHI for HMDB0014429 (Acarbose)

Structure for HMDB0014429 (Acarbose)

3D Structure for HMDB0014429 (Acarbose)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

References

References

References

References