Hmdb loader

Showing metabocard for 5-(Galactosylhydroxy)-L-Lysine (HMDB0242167)

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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-08-27 19:59:31 UTC
Update Date2022-09-22 18:34:34 UTC
HMDB IDHMDB0242167
Secondary Accession NumbersNone
Metabolite Identification
Common Name5-(Galactosylhydroxy)-L-Lysine
Description5-(Galactosylhydroxy)-L-Lysine, also known as hydroxylysine-galactose or beta-1-galactosyl-O-hydroxylysine, belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. Based on a literature review very few articles have been published on 5-(Galactosylhydroxy)-L-Lysine.
Structure
Thumb
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)


  Mrv1652308272122092D          

 29 29  0  0  1  0            999 V2000
    3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1447    4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1447    5.7750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4302    6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158    5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    6.6000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    6.6000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  5  1  1  0  0  0  0
  5  3  1  0  0  0  0
  6  2  1  0  0  0  0
  7  4  1  1  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11  6  1  0  0  0  0
 12 10  1  0  0  0  0
 13  3  1  0  0  0  0
  6 14  1  1  0  0  0
 15  4  1  0  0  0  0
  8 16  1  1  0  0  0
  9 17  1  6  0  0  0
 10 18  1  6  0  0  0
 19 11  2  0  0  0  0
 20 11  1  0  0  0  0
 21  5  1  0  0  0  0
 21 12  1  0  0  0  0
 22  7  1  0  0  0  0
 22 12  1  0  0  0  0
 23  5  1  0  0  0  0
  6 24  1  1  0  0  0
  7 25  1  6  0  0  0
  8 26  1  6  0  0  0
  9 27  1  6  0  0  0
 10 28  1  1  0  0  0
 29 12  1  0  0  0  0
M  END
Download

3D MOL for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

HMDB0242167
     RDKit          3D
5-(Galactosylhydroxy)-L-Lysine
 46 46  0  0  0  0  0  0  0  0999 V2000
    1.4462    0.2654    2.9011 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2068    1.3298    1.9782 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0654    0.9062    0.5522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3272    0.4064   -0.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9385   -0.7925    0.5780 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2041   -1.2420   -0.1251 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2097   -0.2034   -0.1331 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9363   -1.6206   -1.5291 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0840   -2.5204   -1.7921 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754   -1.0391   -2.6186 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0002    0.0250    0.4659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0628    0.4898   -0.2545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2527    0.5660    0.4571 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2721    0.7699   -0.4610 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5120    1.3546    0.1756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2700    2.5851    0.7725 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6450   -0.5627   -1.0597 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4699   -1.2058   -0.1187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3685   -1.3626   -1.2067 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1346   -2.0182   -0.0146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2398   -0.4072   -1.4631 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3999    0.3256   -2.6311 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7986   -0.5266    2.8463 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6103    0.6495    3.8359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2585    1.8320    2.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0490    2.0484    2.0594 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8065    1.8539   -0.0172 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1077    0.2026   -1.1498 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0624    1.2420   -0.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2223   -1.6381    0.5243 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2041   -0.6389    1.6225 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6039   -2.1226    0.4055 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1503    0.4153    0.7121 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1350   -0.6609   -0.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6442   -0.0387   -2.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8848    1.5270   -0.6602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9143    1.4887   -1.2259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9325    0.6787    0.9485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3044    1.4953   -0.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7526    3.3127    0.3050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1387   -0.4861   -2.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4128   -1.0394   -0.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4683   -2.0523   -2.0663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9351   -2.3975    0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3198   -1.0422   -1.6277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9557   -0.1522   -3.2998 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
  6  8  1  0
  8  9  2  0
  8 10  1  0
  3 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
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 12  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  1
  7 33  1  0
  7 34  1  0
 10 35  1  0
 12 36  1  0
 14 37  1  6
 15 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  6
 18 42  1  0
 19 43  1  6
 20 44  1  0
 21 45  1  6
 22 46  1  0
M  END
Download

3D SDF for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)


  Mrv1652308272122092D          

 29 29  0  0  1  0            999 V2000
    3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1447    4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1447    5.7750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4302    6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158    5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    6.6000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    6.6000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  5  1  1  0  0  0  0
  5  3  1  0  0  0  0
  6  2  1  0  0  0  0
  7  4  1  1  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11  6  1  0  0  0  0
 12 10  1  0  0  0  0
 13  3  1  0  0  0  0
  6 14  1  1  0  0  0
 15  4  1  0  0  0  0
  8 16  1  1  0  0  0
  9 17  1  6  0  0  0
 10 18  1  6  0  0  0
 19 11  2  0  0  0  0
 20 11  1  0  0  0  0
 21  5  1  0  0  0  0
 21 12  1  0  0  0  0
 22  7  1  0  0  0  0
 22 12  1  0  0  0  0
 23  5  1  0  0  0  0
  6 24  1  1  0  0  0
  7 25  1  6  0  0  0
  8 26  1  6  0  0  0
  9 27  1  6  0  0  0
 10 28  1  1  0  0  0
 29 12  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0242167

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@](N)(CCC([H])(CN)OC1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O)[C@@]1([H])O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H24N2O8/c13-3-5(1-2-6(14)11(19)20)21-12-10(18)9(17)8(16)7(4-15)22-12/h5-10,12,15-18H,1-4,13-14H2,(H,19,20)/t5?,6-,7+,8-,9-,10+,12?/m0/s1

> <INCHI_KEY>
OWGKYELXGFKIHH-KVUIFDSDSA-N

> <FORMULA>
C12H24N2O8

> <MOLECULAR_WEIGHT>
324.33

> <EXACT_MASS>
324.153265741

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
31.689491657831798

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2,6-diamino-5-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexanoic acid

> <ALOGPS_LOGP>
-3.70

> <JCHEM_LOGP>
-6.252708126450762

> <ALOGPS_LOGS>
-0.73

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.212034819993672

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.848324006648749

> <JCHEM_PKA_STRONGEST_BASIC>
9.801690439238888

> <JCHEM_POLAR_SURFACE_AREA>
188.71999999999997

> <JCHEM_REFRACTIVITY>
71.5843

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.04e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2,6-diamino-5-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

HMDB0242167
     RDKit          3D
5-(Galactosylhydroxy)-L-Lysine
 46 46  0  0  0  0  0  0  0  0999 V2000
    1.4462    0.2654    2.9011 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2068    1.3298    1.9782 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0654    0.9062    0.5522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3272    0.4064   -0.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9385   -0.7925    0.5780 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2041   -1.2420   -0.1251 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2097   -0.2034   -0.1331 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9363   -1.6206   -1.5291 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0840   -2.5204   -1.7921 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754   -1.0391   -2.6186 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0002    0.0250    0.4659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0628    0.4898   -0.2545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2527    0.5660    0.4571 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2721    0.7699   -0.4610 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5120    1.3546    0.1756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2700    2.5851    0.7725 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6450   -0.5627   -1.0597 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4699   -1.2058   -0.1187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3685   -1.3626   -1.2067 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1346   -2.0182   -0.0146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2398   -0.4072   -1.4631 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3999    0.3256   -2.6311 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7986   -0.5266    2.8463 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6103    0.6495    3.8359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2585    1.8320    2.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0490    2.0484    2.0594 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8065    1.8539   -0.0172 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1077    0.2026   -1.1498 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0624    1.2420   -0.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2223   -1.6381    0.5243 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2041   -0.6389    1.6225 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6039   -2.1226    0.4055 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1503    0.4153    0.7121 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1350   -0.6609   -0.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6442   -0.0387   -2.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8848    1.5270   -0.6602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9143    1.4887   -1.2259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9325    0.6787    0.9485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3044    1.4953   -0.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7526    3.3127    0.3050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1387   -0.4861   -2.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4128   -1.0394   -0.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4683   -2.0523   -2.0663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9351   -2.3975    0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3198   -1.0422   -1.6277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9557   -0.1522   -3.2998 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
  6  8  1  0
  8  9  2  0
  8 10  1  0
  3 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
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 12  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  1
  7 33  1  0
  7 34  1  0
 10 35  1  0
 12 36  1  0
 14 37  1  6
 15 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  6
 18 42  1  0
 19 43  1  6
 20 44  1  0
 21 45  1  6
 22 46  1  0
M  END
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PDB for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

HEADER    PROTEIN                                 27-AUG-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-AUG-21         0                                  
HETATM    1  C   UNK     0       6.668   8.470   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335   9.240   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002  10.780   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.670   8.470   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002   9.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001   8.470   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.337   9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.337  10.780   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.003  11.550   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669  10.780   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.669   9.240   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       6.668  11.550   0.000  0.00  0.00           N+0
HETATM   14  N   UNK     0       4.001   6.930   0.000  0.00  0.00           N+0
HETATM   15  O   UNK     0      16.004   9.240   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      14.670  11.550   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      12.003  13.090   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       9.336  11.550   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       1.334   8.470   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       2.667  10.780   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       9.336   8.470   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      12.003   8.470   0.000  0.00  0.00           O+0
HETATM   23  H   UNK     0       6.668  10.010   0.000  0.00  0.00           H+0
HETATM   24  H   UNK     0       4.001  10.010   0.000  0.00  0.00           H+0
HETATM   25  H   UNK     0      14.670  10.010   0.000  0.00  0.00           H+0
HETATM   26  H   UNK     0      13.337  12.320   0.000  0.00  0.00           H+0
HETATM   27  H   UNK     0      12.003  10.010   0.000  0.00  0.00           H+0
HETATM   28  H   UNK     0      10.669  12.320   0.000  0.00  0.00           H+0
HETATM   29  H   UNK     0       9.336  10.010   0.000  0.00  0.00           H+0
CONECT    1    2    5                                                       
CONECT    2    1    6                                                       
CONECT    3    5   13                                                       
CONECT    4    7   15                                                       
CONECT    5    1    3   21   23                                             
CONECT    6    2   11   14   24                                             
CONECT    7    4    8   22   25                                             
CONECT    8    7    9   16   26                                             
CONECT    9    8   10   17   27                                             
CONECT   10    9   12   18   28                                             
CONECT   11    6   19   20                                                  
CONECT   12   10   21   22   29                                             
CONECT   13    3                                                            
CONECT   14    6                                                            
CONECT   15    4                                                            
CONECT   16    8                                                            
CONECT   17    9                                                            
CONECT   18   10                                                            
CONECT   19   11                                                            
CONECT   20   11                                                            
CONECT   21    5   12                                                       
CONECT   22    7   12                                                       
CONECT   23    5                                                            
CONECT   24    6                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27    9                                                            
CONECT   28   10                                                            
CONECT   29   12                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   58    0
END
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3D PDB for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

COMPND    HMDB0242167
HETATM    1  N1  UNL     1       1.446   0.265   2.901  1.00  0.00           N  
HETATM    2  C1  UNL     1       1.207   1.330   1.978  1.00  0.00           C  
HETATM    3  C2  UNL     1       1.065   0.906   0.552  1.00  0.00           C  
HETATM    4  C3  UNL     1       2.327   0.406  -0.084  1.00  0.00           C  
HETATM    5  C4  UNL     1       2.939  -0.792   0.578  1.00  0.00           C  
HETATM    6  C5  UNL     1       4.204  -1.242  -0.125  1.00  0.00           C  
HETATM    7  N2  UNL     1       5.210  -0.203  -0.133  1.00  0.00           N  
HETATM    8  C6  UNL     1       3.936  -1.621  -1.529  1.00  0.00           C  
HETATM    9  O1  UNL     1       3.084  -2.520  -1.792  1.00  0.00           O  
HETATM   10  O2  UNL     1       4.575  -1.039  -2.619  1.00  0.00           O  
HETATM   11  O3  UNL     1      -0.000   0.025   0.466  1.00  0.00           O  
HETATM   12  C7  UNL     1      -1.063   0.490  -0.254  1.00  0.00           C  
HETATM   13  O4  UNL     1      -2.253   0.566   0.457  1.00  0.00           O  
HETATM   14  C8  UNL     1      -3.272   0.770  -0.461  1.00  0.00           C  
HETATM   15  C9  UNL     1      -4.512   1.355   0.176  1.00  0.00           C  
HETATM   16  O5  UNL     1      -4.270   2.585   0.772  1.00  0.00           O  
HETATM   17  C10 UNL     1      -3.645  -0.563  -1.060  1.00  0.00           C  
HETATM   18  O6  UNL     1      -4.470  -1.206  -0.119  1.00  0.00           O  
HETATM   19  C11 UNL     1      -2.368  -1.363  -1.207  1.00  0.00           C  
HETATM   20  O7  UNL     1      -2.135  -2.018  -0.015  1.00  0.00           O  
HETATM   21  C12 UNL     1      -1.240  -0.407  -1.463  1.00  0.00           C  
HETATM   22  O8  UNL     1      -1.400   0.326  -2.631  1.00  0.00           O  
HETATM   23  H1  UNL     1       0.799  -0.527   2.846  1.00  0.00           H  
HETATM   24  H2  UNL     1       1.610   0.650   3.836  1.00  0.00           H  
HETATM   25  H3  UNL     1       0.259   1.832   2.291  1.00  0.00           H  
HETATM   26  H4  UNL     1       2.049   2.048   2.059  1.00  0.00           H  
HETATM   27  H5  UNL     1       0.807   1.854  -0.017  1.00  0.00           H  
HETATM   28  H6  UNL     1       2.108   0.203  -1.150  1.00  0.00           H  
HETATM   29  H7  UNL     1       3.062   1.242  -0.085  1.00  0.00           H  
HETATM   30  H8  UNL     1       2.222  -1.638   0.524  1.00  0.00           H  
HETATM   31  H9  UNL     1       3.204  -0.639   1.623  1.00  0.00           H  
HETATM   32  H10 UNL     1       4.604  -2.123   0.406  1.00  0.00           H  
HETATM   33  H11 UNL     1       5.150   0.415   0.712  1.00  0.00           H  
HETATM   34  H12 UNL     1       6.135  -0.661  -0.210  1.00  0.00           H  
HETATM   35  H13 UNL     1       4.644  -0.039  -2.696  1.00  0.00           H  
HETATM   36  H14 UNL     1      -0.885   1.527  -0.660  1.00  0.00           H  
HETATM   37  H15 UNL     1      -2.914   1.489  -1.226  1.00  0.00           H  
HETATM   38  H16 UNL     1      -4.933   0.679   0.948  1.00  0.00           H  
HETATM   39  H17 UNL     1      -5.304   1.495  -0.587  1.00  0.00           H  
HETATM   40  H18 UNL     1      -4.753   3.313   0.305  1.00  0.00           H  
HETATM   41  H19 UNL     1      -4.139  -0.486  -2.030  1.00  0.00           H  
HETATM   42  H20 UNL     1      -5.413  -1.039  -0.378  1.00  0.00           H  
HETATM   43  H21 UNL     1      -2.468  -2.052  -2.066  1.00  0.00           H  
HETATM   44  H22 UNL     1      -2.935  -2.398   0.398  1.00  0.00           H  
HETATM   45  H23 UNL     1      -0.320  -1.042  -1.628  1.00  0.00           H  
HETATM   46  H24 UNL     1      -1.956  -0.152  -3.300  1.00  0.00           H  
CONECT    1    2   23   24
CONECT    2    3   25   26
CONECT    3    4   11   27
CONECT    4    5   28   29
CONECT    5    6   30   31
CONECT    6    7    8   32
CONECT    7   33   34
CONECT    8    9    9   10
CONECT   10   35
CONECT   11   12
CONECT   12   13   21   36
CONECT   13   14
CONECT   14   15   17   37
CONECT   15   16   38   39
CONECT   16   40
CONECT   17   18   19   41
CONECT   18   42
CONECT   19   20   21   43
CONECT   20   44
CONECT   21   22   45
CONECT   22   46
END
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SMILES for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

[H][C@](N)(CCC([H])(CN)OC1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O)[C@@]1([H])O)C(O)=O
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INCHI for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

InChI=1S/C12H24N2O8/c13-3-5(1-2-6(14)11(19)20)21-12-10(18)9(17)8(16)7(4-15)22-12/h5-10,12,15-18H,1-4,13-14H2,(H,19,20)/t5?,6-,7+,8-,9-,10+,12?/m0/s1
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
GalactosylhydroxylysineHMDB
Hydroxylysine-galactoseHMDB
beta-1-Galactosyl-O-hydroxylysineHMDB
Chemical FormulaC12H24N2O8
Average Molecular Weight324.33
Monoisotopic Molecular Weight324.153265741
IUPAC Name(2S)-2,6-diamino-5-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexanoic acid
Traditional Name(2S)-2,6-diamino-5-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexanoic acid
CAS Registry NumberNot Available
SMILES
[H][C@](N)(CCC([H])(CN)OC1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O)[C@@]1([H])O)C(O)=O
InChI Identifier
InChI=1S/C12H24N2O8/c13-3-5(1-2-6(14)11(19)20)21-12-10(18)9(17)8(16)7(4-15)22-12/h5-10,12,15-18H,1-4,13-14H2,(H,19,20)/t5?,6-,7+,8-,9-,10+,12?/m0/s1
InChI KeyOWGKYELXGFKIHH-KVUIFDSDSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassFatty acyl glycosides
Direct ParentFatty acyl glycosides of mono- and disaccharides
Alternative Parents
Substituents
  • Fatty acyl glycoside of mono- or disaccharide
  • Hexose monosaccharide
  • Glycosyl compound
  • O-glycosyl compound
  • Alpha-amino acid
  • Alpha-amino acid or derivatives
  • L-alpha-amino acid
  • Medium-chain fatty acid
  • Amino fatty acid
  • Heterocyclic fatty acid
  • Hydroxy fatty acid
  • Sugar acid
  • Fatty acid
  • Oxane
  • Monosaccharide
  • Secondary alcohol
  • Amino acid or derivatives
  • Amino acid
  • Organoheterocyclic compound
  • Polyol
  • Acetal
  • Oxacycle
  • Monocarboxylic acid or derivatives
  • Carboxylic acid derivative
  • Carboxylic acid
  • Primary amine
  • Alcohol
  • Organic oxide
  • Organopnictogen compound
  • Primary aliphatic amine
  • Carbonyl group
  • Hydrocarbon derivative
  • Organonitrogen compound
  • Amine
  • Organic oxygen compound
  • Organic nitrogen compound
  • Organooxygen compound
  • Primary alcohol
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
DispositionNot Available
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
logP-3.7ALOGPS
logP-6.3ChemAxon
logS-0.73ALOGPS
pKa (Strongest Acidic)1.85ChemAxon
pKa (Strongest Basic)9.8ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count10ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area188.72 ŲChemAxon
Rotatable Bond Count8ChemAxon
Refractivity71.58 m³·mol⁻¹ChemAxon
Polarizability31.69 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+171.48230932474
DeepCCS[M-H]-169.58630932474
DeepCCS[M-2H]-202.82630932474
DeepCCS[M+Na]+177.64630932474

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Predicted by Siyang on May 30, 202210.1773 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20229.57 minutes32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid426.8 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid256.2 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid29.8 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid182.6 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid80.2 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid337.9 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid265.8 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)1094.9 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid575.2 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid54.6 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid676.5 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid205.7 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid309.7 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate1042.8 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA817.0 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water530.2 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
5-(Galactosylhydroxy)-L-Lysine[H][C@](N)(CCC([H])(CN)OC1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O)[C@@]1([H])O)C(O)=O3494.2Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine[H][C@](N)(CCC([H])(CN)OC1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O)[C@@]1([H])O)C(O)=O3255.6Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine[H][C@](N)(CCC([H])(CN)OC1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O)[C@@]1([H])O)C(O)=O2850.0Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #1C[Si](C)(C)NCC(CC[C@H](N)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2635.6Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #1C[Si](C)(C)NCC(CC[C@H](N)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2852.1Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #1C[Si](C)(C)NCC(CC[C@H](N)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3711.3Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #10C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2931.9Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #10C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C3018.8Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #10C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C3463.6Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #11C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2718.4Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #11C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2943.6Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #11C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O3260.9Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #12C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2838.3Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #12C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2962.3Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #12C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3770.5Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #13C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2844.3Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #13C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2955.6Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #13C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3709.3Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #14C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C2948.6Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #14C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C3025.1Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #14C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C3405.4Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #15C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2910.8Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #15C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O3013.5Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #15C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O3379.8Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #16C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)C(=O)O[Si](C)(C)C2937.6Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #16C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)C(=O)O[Si](C)(C)C3034.6Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #16C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)C(=O)O[Si](C)(C)C3467.3Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #17C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2905.8Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #17C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O3021.7Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #17C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O3443.9Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #18C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O3155.1Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #18C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O3117.4Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #18C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O3607.2Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #19C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2779.7Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #19C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2910.3Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #19C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3297.6Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #2C[Si](C)(C)N[C@@H](CCC(CN)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C2679.1Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #2C[Si](C)(C)N[C@@H](CCC(CN)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C2849.3Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #2C[Si](C)(C)N[C@@H](CCC(CN)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3661.1Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #20C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2859.3Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #20C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2925.4Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #20C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3901.7Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #21C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2856.9Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #21C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2923.1Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #21C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3723.7Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #22C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O2977.5Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #22C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O2987.3Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #22C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O3463.8Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #23C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2922.1Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #23C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2984.2Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #23C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3415.1Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #24C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O2972.5Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #24C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O3013.9Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #24C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O3505.3Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #25C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2919.6Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #25C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C3007.9Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #25C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C3458.2Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #26C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O3154.6Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #26C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O3112.5Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #26C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O3627.9Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #27C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O2966.2Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #27C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O2999.0Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #27C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O3459.1Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #28C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2900.0Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #28C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2998.5Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #28C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O3406.9Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #29C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O3143.0Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #29C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O3094.4Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #29C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O3548.5Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #3C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2721.0Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #3C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2929.9Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #3C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3266.8Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #30C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C3132.8Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #30C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C3112.1Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #30C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C3609.0Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #31C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2720.9Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #31C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2914.0Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #31C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3197.2Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #32C[Si](C)(C)OC(=O)[C@H](CCC(CN)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2856.6Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #32C[Si](C)(C)OC(=O)[C@H](CCC(CN)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2938.5Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #32C[Si](C)(C)OC(=O)[C@H](CCC(CN)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3668.6Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #33C[Si](C)(C)OC(=O)[C@@H](N)CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2851.4Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #33C[Si](C)(C)OC(=O)[C@@H](N)CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2944.0Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #33C[Si](C)(C)OC(=O)[C@@H](N)CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3735.7Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #34C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C2953.5Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #34C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C3011.1Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #34C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C3350.9Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #35C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2912.2Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #35C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O3001.8Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #35C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O3324.9Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #36C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C2967.3Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #36C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3019.3Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #36C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3408.7Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #37C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2929.8Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #37C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C3004.2Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #37C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C3387.6Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #38C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C3170.5Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #38C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C3112.5Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #38C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C3530.4Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #39C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O2983.5Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #39C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O2975.5Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #39C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O3395.7Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #4C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O2866.7Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #4C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O2956.1Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #4C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O3781.1Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #40C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2924.0Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #40C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2974.8Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #40C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3346.6Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #41C[Si](C)(C)O[C@H]1C(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O3161.1Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #41C[Si](C)(C)O[C@H]1C(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O3099.5Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #41C[Si](C)(C)O[C@H]1C(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O3544.5Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #42C[Si](C)(C)O[C@H]1[C@@H](CO)OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C3139.4Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #42C[Si](C)(C)O[C@H]1[C@@H](CO)OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C3082.0Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #42C[Si](C)(C)O[C@H]1[C@@H](CO)OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C3496.0Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #43C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C2962.3Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #43C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C2994.2Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #43C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3354.4Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #44C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2925.7Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #44C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2982.0Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #44C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3332.3Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #45C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C3182.5Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #45C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C3086.6Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #45C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C3472.9Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #46C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3157.2Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #46C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3070.6Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #46C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3501.4Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #47C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3184.5Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #47C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3107.1Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #47C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3548.8Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #5C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O2869.5Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #5C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O2946.3Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #5C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O3715.2Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #6C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2728.4Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #6C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2947.2Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #6C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C3317.9Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #7C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C2856.5Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #7C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C2980.4Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #7C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C3811.2Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #8C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C2858.9Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #8C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C2970.7Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #8C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C3745.3Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C2954.2Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3035.9Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3483.0Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #1C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2726.7Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #1C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2975.0Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #1C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3076.5Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #10C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2904.2Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #10C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O3056.4Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #10C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O3187.2Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #11C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O3174.7Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #11C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O3130.1Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #11C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O3314.8Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #12C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C3156.8Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #12C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C3137.0Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #12C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C3362.3Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #13C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O2979.8Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #13C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O3023.4Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #13C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O3240.5Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #14C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2919.6Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #14C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3028.7Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #14C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3195.5Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #15C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O3173.9Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #15C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O3098.3Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #15C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O3342.5Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #16C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C3167.4Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #16C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C3125.3Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #16C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C3371.9Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #17C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3153.9Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #17C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3111.7Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #17C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3339.2Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #18C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C2940.2Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #18C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3035.0Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #18C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3152.6Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #19C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2910.1Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #19C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3031.2Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #19C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3130.2Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #2C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2834.5Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #2C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2983.1Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #2C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3649.5Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #20C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C3163.6Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #20C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C3119.4Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #20C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C3271.0Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #21C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3191.6Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #21C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3125.4Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #21C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3312.3Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #22C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)O[C@@H]1CO3168.8Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #22C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)O[C@@H]1CO3090.9Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #22C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)O[C@@H]1CO3285.9Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #23C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3183.7Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #23C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3101.8Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #23C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3274.1Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #3C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2859.2Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #3C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2972.2Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #3C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3588.6Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #4C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C2941.3Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #4C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3045.3Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #4C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3214.7Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #5C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2916.0Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #5C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3039.9Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #5C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3191.5Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #6C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C2936.6Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #6C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3068.6Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #6C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3251.8Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #7C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2908.6Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #7C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C3062.0Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #7C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C3229.5Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #8C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O3183.0Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #8C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O3139.3Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #8C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O3374.7Standard polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C2932.4Semi standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C3060.3Standard non polar33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C3212.9Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine GC-MS (Non-derivatized) - 70eV, Positivesplash10-001i-9351000000-2b0869d6c5a1463ed7322021-09-23Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine 10V, Positive-QTOFsplash10-0a6u-0149000000-4e725e817251be240bac2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine 20V, Positive-QTOFsplash10-004i-2922000000-37a84b130e322e5241922021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine 40V, Positive-QTOFsplash10-0a4i-6900000000-eef35112d83ae805dfe12021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine 10V, Negative-QTOFsplash10-0c03-0908000000-de95cb3f8a83dd21606b2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine 20V, Negative-QTOFsplash10-01ox-2901000000-201eaa6808fc292a80dd2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine 40V, Negative-QTOFsplash10-0apl-9600000000-b55c13de022050e6e47a2021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Blood
  • Urine
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedCancer patients undergoing total body irradiation details
UrineDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedCancer patients undergoing total body irradiation details
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID65792395
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound66995551
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Kong SW, Hernandez-Ferrer C: Assessment of coverage for endogenous metabolites and exogenous chemical compounds using an untargeted metabolomics platform. Pac Symp Biocomput. 2020;25:587-598. [PubMed:31797630 ]