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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2013-05-09 20:52:52 UTC

Update Date

2022-03-07 03:17:38 UTC

HMDB ID

HMDB0060077

Secondary Accession Numbers

HMDB60077

Metabolite Identification

Common Name

cis-Melilotoside

Description

cis-Melilotoside, also known as cis-beta-D-glucosyl-2-hydroxycinnamate or cis-coumarinic acid-beta-D-glucoside, belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans and flavonoids. cis-Melilotoside is an extremely weak basic (essentially neutral) compound (based on its pKa) and is a beta-D-glucoside consisting of cis-2-coumaric acid having a beta-D-glucosyl residue attached to the phenolic hydroxy group. cis-Melilotoside has been detected, but not quantified in, several different foods, such as globe artichokes, mentha (mint), Malabar spinach, plains prickly pears, and winter savouries. This could make cis-melilotoside a potential biomarker for the consumption of these foods.

Structure

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

HMDB0060077
     RDKit          3D
cis-Melilotoside
 41 42  0  0  0  0  0  0  0  0999 V2000
    5.3135   -0.2438    0.8842 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1082    0.6908    0.0866 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1855    1.6223    0.0189 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9933    0.9719   -0.7510 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9026    0.3065   -0.9570 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5695   -0.9583   -0.3563 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4960   -1.9265   -0.1216 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1059   -3.0783    0.5729 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8295   -3.2831    1.0282 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9179   -2.2772    0.7659 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2374   -1.1430    0.1017 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3414   -0.1679   -0.1492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9981   -0.0438    0.1539 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8236    0.0292   -0.9719 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1539    0.0687   -0.5595 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0233   -0.1272   -1.7839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7687   -1.3473   -2.4008 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5075    1.4012    0.0643 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1311    1.2735    1.2898 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2118    2.1545    0.2818 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7561    2.6771   -0.9034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2504    1.2270    0.9531 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7856    0.8386    2.1789 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9873    2.5622    0.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0697    1.9495   -1.3424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1629    0.7621   -1.6632 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5259   -1.9094   -0.5087 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8520   -3.8472    0.7598 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5245   -4.1713    1.5649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1030   -2.4591    1.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3378   -0.9423    0.7039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3772   -0.7162    0.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1091   -0.0720   -1.5111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8721    0.6875   -2.5278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4552   -1.9708   -1.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1291    2.0239   -0.6163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1570    0.3538    1.6408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3974    2.9969    0.9763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7730    2.7584   -0.9567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3182    1.7740    1.1704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6842    1.5549    2.8756 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 11  6  1  0
 22 13  1  0
  3 24  1  0
  4 25  1  0
  5 26  1  0
  7 27  1  0
  8 28  1  0
  9 29  1  0
 10 30  1  0
 13 31  1  1
 15 32  1  1
 16 33  1  0
 16 34  1  0
 17 35  1  0
 18 36  1  6
 19 37  1  0
 20 38  1  1
 21 39  1  0
 22 40  1  1
 23 41  1  0
M  END


  Mrv1652309042000402D          

 23 24  0  0  0  0            999 V2000
10000.0216 9999.8039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.5923 9998.9786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.4492 9998.9786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.592310002.2791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.1610 9999.8039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.1631 9998.5652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.877710002.6917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.161010001.4539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.592310001.4538    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9997.877810001.0413    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9997.877810000.2162    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9998.5923 9999.8038    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9999.306810000.2162    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9999.306810001.0413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.449910001.4538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.735510001.0413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.735510000.2162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.4499 9999.8037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.164410000.2162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.164410001.0413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.8778 9998.9772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.8784 9999.8022    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.5920 9998.5642    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  6  2  0  0  0  0
  4  7  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 14  1  0  0  0  0
 13 14  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 15  1  0  0  0  0
  1 17  1  0  0  0  0
 18  3  1  0  0  0  0
 13  1  1  1  0  0  0
 12  2  1  6  0  0  0
  9  4  1  1  0  0  0
 11  5  1  1  0  0  0
 10  8  1  6  0  0  0
  6 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0060077

> <DATABASE_NAME>
hmdb

> <SMILES>
OC[C@H]1O[C@@H](OC2=C(\C=C/C(O)=O)C=CC=C2)[C@H](O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C15H18O8/c16-7-10-12(19)13(20)14(21)15(23-10)22-9-4-2-1-3-8(9)5-6-11(17)18/h1-6,10,12-16,19-21H,7H2,(H,17,18)/b6-5-/t10-,12-,13+,14-,15-/m1/s1

> <INCHI_KEY>
GVRIYIMNJGULCZ-QLFWQTQQSA-N

> <FORMULA>
C15H18O8

> <MOLECULAR_WEIGHT>
326.2986

> <EXACT_MASS>
326.100167552

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
31.48046575536168

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-0.70

> <JCHEM_LOGP>
-0.43554715499999985

> <ALOGPS_LOGS>
-1.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.200113282770712

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.202715684013416

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810923461838152

> <JCHEM_POLAR_SURFACE_AREA>
136.68

> <JCHEM_REFRACTIVITY>
77.18520000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.60e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
cis-melilotoside

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0060077
     RDKit          3D
cis-Melilotoside
 41 42  0  0  0  0  0  0  0  0999 V2000
    5.3135   -0.2438    0.8842 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1082    0.6908    0.0866 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1855    1.6223    0.0189 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9933    0.9719   -0.7510 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9026    0.3065   -0.9570 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5695   -0.9583   -0.3563 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4960   -1.9265   -0.1216 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1059   -3.0783    0.5729 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8295   -3.2831    1.0282 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9179   -2.2772    0.7659 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2374   -1.1430    0.1017 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3414   -0.1679   -0.1492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9981   -0.0438    0.1539 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8236    0.0292   -0.9719 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1539    0.0687   -0.5595 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0233   -0.1272   -1.7839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7687   -1.3473   -2.4008 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5075    1.4012    0.0643 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1311    1.2735    1.2898 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2118    2.1545    0.2818 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7561    2.6771   -0.9034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2504    1.2270    0.9531 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7856    0.8386    2.1789 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9873    2.5622    0.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0697    1.9495   -1.3424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1629    0.7621   -1.6632 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5259   -1.9094   -0.5087 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8520   -3.8472    0.7598 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5245   -4.1713    1.5649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1030   -2.4591    1.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3378   -0.9423    0.7039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3772   -0.7162    0.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1091   -0.0720   -1.5111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8721    0.6875   -2.5278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4552   -1.9708   -1.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1291    2.0239   -0.6163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1570    0.3538    1.6408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3974    2.9969    0.9763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7730    2.7584   -0.9567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3182    1.7740    1.1704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6842    1.5549    2.8756 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 11  6  1  0
 22 13  1  0
  3 24  1  0
  4 25  1  0
  5 26  1  0
  7 27  1  0
  8 28  1  0
  9 29  1  0
 10 30  1  0
 13 31  1  1
 15 32  1  1
 16 33  1  0
 16 34  1  0
 17 35  1  0
 18 36  1  6
 19 37  1  0
 20 38  1  1
 21 39  1  0
 22 40  1  1
 23 41  1  0
M  END

HEADER    PROTEIN                                 04-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-20         0                                  
HETATM    1  O   UNK     0    8666.7078666.301   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0    8664.0398664.760   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0    8669.3728664.760   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8664.0398670.921   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0    8661.3678666.301   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0    8670.7048663.988   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0    8662.7058671.691   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0    8661.3678669.381   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0    8664.0398669.380   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8662.7058668.610   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8662.7058667.070   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8664.0398666.300   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8665.3738667.070   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0    8665.3738668.610   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0    8669.3738669.380   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8668.0408668.610   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8668.0408667.070   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    8669.3738666.300   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8670.7078667.070   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8670.7078668.610   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8672.0398664.757   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0    8672.0408666.297   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0    8673.3728663.987   0.000  0.00  0.00           O+0
CONECT    1   17   13                                                       
CONECT    2   12                                                            
CONECT    3    6   18                                                       
CONECT    4    7    9                                                       
CONECT    5   11                                                            
CONECT    6    3   21                                                       
CONECT    7    4                                                            
CONECT    8   10                                                            
CONECT    9   10   14    4                                                  
CONECT   10    9   11    8                                                  
CONECT   11   10   12    5                                                  
CONECT   12   11   13    2                                                  
CONECT   13   12   14    1                                                  
CONECT   14    9   13                                                       
CONECT   15   16   20                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18    1                                                  
CONECT   18   17   19    3                                                  
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21    6   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

COMPND    HMDB0060077
HETATM    1  O1  UNL     1       5.314  -0.244   0.884  1.00  0.00           O  
HETATM    2  C1  UNL     1       5.108   0.691   0.087  1.00  0.00           C  
HETATM    3  O2  UNL     1       6.186   1.622   0.019  1.00  0.00           O  
HETATM    4  C2  UNL     1       3.993   0.972  -0.751  1.00  0.00           C  
HETATM    5  C3  UNL     1       2.903   0.307  -0.957  1.00  0.00           C  
HETATM    6  C4  UNL     1       2.569  -0.958  -0.356  1.00  0.00           C  
HETATM    7  C5  UNL     1       3.496  -1.926  -0.122  1.00  0.00           C  
HETATM    8  C6  UNL     1       3.106  -3.078   0.573  1.00  0.00           C  
HETATM    9  C7  UNL     1       1.830  -3.283   1.028  1.00  0.00           C  
HETATM   10  C8  UNL     1       0.918  -2.277   0.766  1.00  0.00           C  
HETATM   11  C9  UNL     1       1.237  -1.143   0.102  1.00  0.00           C  
HETATM   12  O3  UNL     1       0.341  -0.168  -0.149  1.00  0.00           O  
HETATM   13  C10 UNL     1      -0.998  -0.044   0.154  1.00  0.00           C  
HETATM   14  O4  UNL     1      -1.824   0.029  -0.972  1.00  0.00           O  
HETATM   15  C11 UNL     1      -3.154   0.069  -0.560  1.00  0.00           C  
HETATM   16  C12 UNL     1      -4.023  -0.127  -1.784  1.00  0.00           C  
HETATM   17  O5  UNL     1      -3.769  -1.347  -2.401  1.00  0.00           O  
HETATM   18  C13 UNL     1      -3.507   1.401   0.064  1.00  0.00           C  
HETATM   19  O6  UNL     1      -4.131   1.273   1.290  1.00  0.00           O  
HETATM   20  C14 UNL     1      -2.212   2.155   0.282  1.00  0.00           C  
HETATM   21  O7  UNL     1      -1.756   2.677  -0.903  1.00  0.00           O  
HETATM   22  C15 UNL     1      -1.250   1.227   0.953  1.00  0.00           C  
HETATM   23  O8  UNL     1      -1.786   0.839   2.179  1.00  0.00           O  
HETATM   24  H1  UNL     1       5.987   2.562   0.395  1.00  0.00           H  
HETATM   25  H2  UNL     1       4.070   1.950  -1.342  1.00  0.00           H  
HETATM   26  H3  UNL     1       2.163   0.762  -1.663  1.00  0.00           H  
HETATM   27  H4  UNL     1       4.526  -1.909  -0.509  1.00  0.00           H  
HETATM   28  H5  UNL     1       3.852  -3.847   0.760  1.00  0.00           H  
HETATM   29  H6  UNL     1       1.525  -4.171   1.565  1.00  0.00           H  
HETATM   30  H7  UNL     1      -0.103  -2.459   1.137  1.00  0.00           H  
HETATM   31  H8  UNL     1      -1.338  -0.942   0.704  1.00  0.00           H  
HETATM   32  H9  UNL     1      -3.377  -0.716   0.165  1.00  0.00           H  
HETATM   33  H10 UNL     1      -5.109  -0.072  -1.511  1.00  0.00           H  
HETATM   34  H11 UNL     1      -3.872   0.687  -2.528  1.00  0.00           H  
HETATM   35  H12 UNL     1      -3.455  -1.971  -1.688  1.00  0.00           H  
HETATM   36  H13 UNL     1      -4.129   2.024  -0.616  1.00  0.00           H  
HETATM   37  H14 UNL     1      -4.157   0.354   1.641  1.00  0.00           H  
HETATM   38  H15 UNL     1      -2.397   2.997   0.976  1.00  0.00           H  
HETATM   39  H16 UNL     1      -0.773   2.758  -0.957  1.00  0.00           H  
HETATM   40  H17 UNL     1      -0.318   1.774   1.170  1.00  0.00           H  
HETATM   41  H18 UNL     1      -1.684   1.555   2.876  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    4
CONECT    3   24
CONECT    4    5    5   25
CONECT    5    6   26
CONECT    6    7    7   11
CONECT    7    8   27
CONECT    8    9    9   28
CONECT    9   10   29
CONECT   10   11   11   30
CONECT   11   12
CONECT   12   13
CONECT   13   14   22   31
CONECT   14   15
CONECT   15   16   18   32
CONECT   16   17   33   34
CONECT   17   35
CONECT   18   19   20   36
CONECT   19   37
CONECT   20   21   22   38
CONECT   21   39
CONECT   22   23   40
CONECT   23   41
END

HMDB0060077
     RDKit          3D
cis-Melilotoside
 41 42  0  0  0  0  0  0  0  0999 V2000
    5.3135   -0.2438    0.8842 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1082    0.6908    0.0866 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1855    1.6223    0.0189 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9933    0.9719   -0.7510 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9026    0.3065   -0.9570 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5695   -0.9583   -0.3563 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4960   -1.9265   -0.1216 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1059   -3.0783    0.5729 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8295   -3.2831    1.0282 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9179   -2.2772    0.7659 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2374   -1.1430    0.1017 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3414   -0.1679   -0.1492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9981   -0.0438    0.1539 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8236    0.0292   -0.9719 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1539    0.0687   -0.5595 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0233   -0.1272   -1.7839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7687   -1.3473   -2.4008 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5075    1.4012    0.0643 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1311    1.2735    1.2898 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2118    2.1545    0.2818 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7561    2.6771   -0.9034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2504    1.2270    0.9531 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7856    0.8386    2.1789 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9873    2.5622    0.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0697    1.9495   -1.3424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1629    0.7621   -1.6632 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5259   -1.9094   -0.5087 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8520   -3.8472    0.7598 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5245   -4.1713    1.5649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1030   -2.4591    1.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3378   -0.9423    0.7039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3772   -0.7162    0.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1091   -0.0720   -1.5111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8721    0.6875   -2.5278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4552   -1.9708   -1.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1291    2.0239   -0.6163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1570    0.3538    1.6408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3974    2.9969    0.9763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7730    2.7584   -0.9567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3182    1.7740    1.1704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6842    1.5549    2.8756 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 11  6  1  0
 22 13  1  0
  3 24  1  0
  4 25  1  0
  5 26  1  0
  7 27  1  0
  8 28  1  0
  9 29  1  0
 10 30  1  0
 13 31  1  1
 15 32  1  1
 16 33  1  0
 16 34  1  0
 17 35  1  0
 18 36  1  6
 19 37  1  0
 20 38  1  1
 21 39  1  0
 22 40  1  1
 23 41  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
(2Z)-3-[2-(beta-D-Glucopyranosyloxy)phenyl]acrylic acid	ChEBI
beta-D-Glucosyl-2-coumarinate	ChEBI
beta-D-Glucosyl-2-coumarinic acid	ChEBI
cis-beta-D-Glucosyl-2-hydroxycinnamic acid	ChEBI
cis-Coumarinic acid-beta-D-glucoside	ChEBI
cis-Melilotoside	ChEBI
(2Z)-3-[2-(b-D-Glucopyranosyloxy)phenyl]acrylate	Generator
(2Z)-3-[2-(b-D-Glucopyranosyloxy)phenyl]acrylic acid	Generator
(2Z)-3-[2-(beta-D-Glucopyranosyloxy)phenyl]acrylate	Generator
(2Z)-3-[2-(β-D-Glucopyranosyloxy)phenyl]acrylate	Generator
(2Z)-3-[2-(β-D-Glucopyranosyloxy)phenyl]acrylic acid	Generator
cis-Coumarinate-β-D-glucoside	Generator
b-D-Glucosyl-2-coumarinate	Generator
b-D-Glucosyl-2-coumarinic acid	Generator
β-D-Glucosyl-2-coumarinate	Generator
β-D-Glucosyl-2-coumarinic acid	Generator
cis-b-D-Glucosyl-2-hydroxycinnamate	Generator
cis-b-D-Glucosyl-2-hydroxycinnamic acid	Generator
cis-beta-D-Glucosyl-2-hydroxycinnamate	Generator
cis-β-D-Glucosyl-2-hydroxycinnamate	Generator
cis-β-D-Glucosyl-2-hydroxycinnamic acid	Generator
cis-Coumarinate-b-D-glucoside	Generator
cis-Coumarinate-beta-D-glucoside	Generator
cis-Coumarinic acid-b-D-glucoside	Generator
cis-Coumarinic acid-β-D-glucoside	Generator
(2Z)-3-[2-(beta-D-Glucopyranosyloxy)phenyl]-2-propenoic acid	HMDB
(2Z)-3-[2-(β-D-Glucopyranosyloxy)phenyl]-2-propenoic acid	HMDB
2'-(beta-D-Glucopyranosyloxy)cinnamic acid	HMDB
2'-(β-D-Glucopyranosyloxy)cinnamic acid	HMDB
2’-(β-D-Glucopyranosyloxy)cinnamic acid	HMDB
3-[2-(beta-D-Glucopyranosyloxy)phenyl]-2-propenoic acid	HMDB
3-[2-(β-D-Glucopyranosyloxy)phenyl]-2-propenoic acid	HMDB
Coumarin glucoside	HMDB
Coumarinate glucoside	HMDB
Coumarinic acid glucoside	HMDB
beta-D-Glucosyl-2-coumarate	HMDB
beta-D-Glucosyl-2-coumaric acid	HMDB
cis-o-Hydroxycinnamic acid glucoside	HMDB
o-(Glucosyloxy)cinnamic acid	HMDB
o-Coumaroyl beta-D-glucopyranoside	HMDB
o-Coumaroyl β-D-glucopyranoside	HMDB
β-D-Glucosyl-2-coumarate	HMDB
β-D-Glucosyl-2-coumaric acid	HMDB

Chemical Formula

C₁₅H₁₈O₈

Average Molecular Weight

326.2986

Monoisotopic Molecular Weight

326.100167552

IUPAC Name

(2Z)-3-(2-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoic acid

Traditional Name

cis-melilotoside

CAS Registry Number

2446-60-8

SMILES

OC[C@H]1O[C@@H](OC2=C(\C=C/C(O)=O)C=CC=C2)[C@H](O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C15H18O8/c16-7-10-12(19)13(20)14(21)15(23-10)22-9-4-2-1-3-8(9)5-6-11(17)18/h1-6,10,12-16,19-21H,7H2,(H,17,18)/b6-5-/t10-,12-,13+,14-,15-/m1/s1

InChI Key

GVRIYIMNJGULCZ-QLFWQTQQSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Cinnamic acid
Cinnamic acid or derivatives
Coumaric acid
Coumaric acid or derivatives
Hexose monosaccharide
O-glycosyl compound
Styrene
Phenol ether
Phenoxy compound
Benzenoid
Monocyclic benzene moiety
Oxane
Monosaccharide
Secondary alcohol
Polyol
Carboxylic acid derivative
Carboxylic acid
Acetal
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Primary alcohol
Organic oxide
Hydrocarbon derivative
Carbonyl group
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

beta-D-glucoside (CHEBI:62251 )
Monolignols (C05839 )

Ontology

Not Available

Exogenous (HMDB: HMDB0060077)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	6.6 g/L	ALOGPS
logP	-0.7	ALOGPS
logP	-0.44	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	3.2	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.68 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	77.19 m³·mol⁻¹	ChemAxon
Polarizability	31.48 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	174.361	31661259
DarkChem	[M-H]-	169.566	31661259
DeepCCS	[M+H]+	168.336	30932474
DeepCCS	[M-H]-	165.941	30932474
DeepCCS	[M-2H]-	199.706	30932474
DeepCCS	[M+Na]+	174.528	30932474
AllCCS	[M+H]+	175.7	32859911
AllCCS	[M+H-H2O]+	172.6	32859911
AllCCS	[M+NH4]+	178.6	32859911
AllCCS	[M+Na]+	179.4	32859911
AllCCS	[M-H]-	172.3	32859911
AllCCS	[M+Na-2H]-	172.3	32859911
AllCCS	[M+HCOO]-	172.3	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.	3.08 minutes	32390414
Predicted by Siyang on May 30, 2022	10.2711 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	5.38 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1246.5 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	229.6 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	86.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	179.6 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	72.4 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	287.3 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	317.0 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	433.0 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	679.8 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	279.7 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	937.1 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	198.6 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	230.3 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	436.0 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	272.4 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	112.4 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
cis-Melilotoside	OC[C@H]1O[C@@H](OC2=C(\C=C/C(O)=O)C=CC=C2)[C@H](O)[C@@H](O)[C@@H]1O	4771.8	Standard polar	33892256
cis-Melilotoside	OC[C@H]1O[C@@H](OC2=C(\C=C/C(O)=O)C=CC=C2)[C@H](O)[C@@H](O)[C@@H]1O	3017.0	Standard non polar	33892256
cis-Melilotoside	OC[C@H]1O[C@@H](OC2=C(\C=C/C(O)=O)C=CC=C2)[C@H](O)[C@@H](O)[C@@H]1O	2921.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
cis-Melilotoside,1TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O)[C@@H](O)[C@@H]1O	2891.0	Semi standard non polar	33892256
cis-Melilotoside,1TMS,isomer #2	C[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2908.5	Semi standard non polar	33892256
cis-Melilotoside,1TMS,isomer #3	C[Si](C)(C)O[C@H]1[C@H](OC2=CC=CC=C2/C=C\C(=O)O)O[C@H](CO)[C@@H](O)[C@@H]1O	2878.9	Semi standard non polar	33892256
cis-Melilotoside,1TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC=CC=C2/C=C\C(=O)O)O[C@H](CO)[C@H]1O	2875.2	Semi standard non polar	33892256
cis-Melilotoside,1TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O)[C@H]1O	2882.5	Semi standard non polar	33892256
cis-Melilotoside,2TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2842.2	Semi standard non polar	33892256
cis-Melilotoside,2TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O)[C@H]1O[Si](C)(C)C	2834.1	Semi standard non polar	33892256
cis-Melilotoside,2TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2828.6	Semi standard non polar	33892256
cis-Melilotoside,2TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2839.9	Semi standard non polar	33892256
cis-Melilotoside,2TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2843.6	Semi standard non polar	33892256
cis-Melilotoside,2TMS,isomer #5	C[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2855.0	Semi standard non polar	33892256
cis-Melilotoside,2TMS,isomer #6	C[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2852.3	Semi standard non polar	33892256
cis-Melilotoside,2TMS,isomer #7	C[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2864.4	Semi standard non polar	33892256
cis-Melilotoside,2TMS,isomer #8	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC=CC=C2/C=C\C(=O)O)O[C@@H]1CO	2847.0	Semi standard non polar	33892256
cis-Melilotoside,2TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC=CC=C2/C=C\C(=O)O)O[C@H](CO)[C@H]1O	2834.9	Semi standard non polar	33892256
cis-Melilotoside,3TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2804.0	Semi standard non polar	33892256
cis-Melilotoside,3TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC=CC=C2/C=C\C(=O)O)O[C@H](CO)[C@H]1O[Si](C)(C)C	2830.3	Semi standard non polar	33892256
cis-Melilotoside,3TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2814.4	Semi standard non polar	33892256
cis-Melilotoside,3TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2809.1	Semi standard non polar	33892256
cis-Melilotoside,3TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2823.5	Semi standard non polar	33892256
cis-Melilotoside,3TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2848.5	Semi standard non polar	33892256
cis-Melilotoside,3TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2830.7	Semi standard non polar	33892256
cis-Melilotoside,3TMS,isomer #7	C[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2810.8	Semi standard non polar	33892256
cis-Melilotoside,3TMS,isomer #8	C[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2825.2	Semi standard non polar	33892256
cis-Melilotoside,3TMS,isomer #9	C[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2810.6	Semi standard non polar	33892256
cis-Melilotoside,4TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2804.7	Semi standard non polar	33892256
cis-Melilotoside,4TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2836.8	Semi standard non polar	33892256
cis-Melilotoside,4TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2819.1	Semi standard non polar	33892256
cis-Melilotoside,4TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2867.3	Semi standard non polar	33892256
cis-Melilotoside,4TMS,isomer #5	C[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2809.5	Semi standard non polar	33892256
cis-Melilotoside,5TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[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	2838.6	Semi standard non polar	33892256
cis-Melilotoside,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O)[C@@H](O)[C@@H]1O	3143.8	Semi standard non polar	33892256
cis-Melilotoside,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3158.1	Semi standard non polar	33892256
cis-Melilotoside,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC=CC=C2/C=C\C(=O)O)O[C@H](CO)[C@@H](O)[C@@H]1O	3144.0	Semi standard non polar	33892256
cis-Melilotoside,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC=CC=C2/C=C\C(=O)O)O[C@H](CO)[C@H]1O	3144.4	Semi standard non polar	33892256
cis-Melilotoside,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O)[C@H]1O	3147.3	Semi standard non polar	33892256
cis-Melilotoside,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3351.3	Semi standard non polar	33892256
cis-Melilotoside,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3324.6	Semi standard non polar	33892256
cis-Melilotoside,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3316.7	Semi standard non polar	33892256
cis-Melilotoside,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3330.1	Semi standard non polar	33892256
cis-Melilotoside,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3325.0	Semi standard non polar	33892256
cis-Melilotoside,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3362.5	Semi standard non polar	33892256
cis-Melilotoside,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3369.7	Semi standard non polar	33892256
cis-Melilotoside,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3377.8	Semi standard non polar	33892256
cis-Melilotoside,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC=CC=C2/C=C\C(=O)O)O[C@@H]1CO	3332.1	Semi standard non polar	33892256
cis-Melilotoside,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC=CC=C2/C=C\C(=O)O)O[C@H](CO)[C@H]1O	3325.0	Semi standard non polar	33892256
cis-Melilotoside,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3550.6	Semi standard non polar	33892256
cis-Melilotoside,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC=CC=C2/C=C\C(=O)O)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C	3485.8	Semi standard non polar	33892256
cis-Melilotoside,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3539.4	Semi standard non polar	33892256
cis-Melilotoside,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3540.5	Semi standard non polar	33892256
cis-Melilotoside,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3480.2	Semi standard non polar	33892256
cis-Melilotoside,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3526.1	Semi standard non polar	33892256
cis-Melilotoside,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3489.2	Semi standard non polar	33892256
cis-Melilotoside,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3528.2	Semi standard non polar	33892256
cis-Melilotoside,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3551.5	Semi standard non polar	33892256
cis-Melilotoside,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3535.0	Semi standard non polar	33892256
cis-Melilotoside,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3682.1	Semi standard non polar	33892256
cis-Melilotoside,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3716.3	Semi standard non polar	33892256
cis-Melilotoside,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3685.2	Semi standard non polar	33892256
cis-Melilotoside,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3702.4	Semi standard non polar	33892256
cis-Melilotoside,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)/C=C\C1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3665.5	Semi standard non polar	33892256
cis-Melilotoside,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=CC=C2/C=C\C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3878.3	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 - cis-Melilotoside GC-MS (Non-derivatized) - 70eV, Positive	splash10-0zfr-5943000000-c492ad4cea7748c10d1d	2017-09-20	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Melilotoside GC-MS (5 TMS) - 70eV, Positive	splash10-00di-1020229000-cd5e122c29a7c414bbb3	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Melilotoside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Melilotoside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Melilotoside 10V, Positive-QTOF	splash10-0aos-0937000000-443e87b5dc30d11c2254	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Melilotoside 20V, Positive-QTOF	splash10-014j-0900000000-efd45bdfdb0cc42c2cb9	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Melilotoside 40V, Positive-QTOF	splash10-066r-2900000000-be6e64ff24e527eb6506	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Melilotoside 10V, Negative-QTOF	splash10-01t9-0829000000-6df80077de9156a07096	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Melilotoside 20V, Negative-QTOF	splash10-03di-1911000000-4ab9ec4cd0e2b2cb4feb	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Melilotoside 40V, Negative-QTOF	splash10-0295-2900000000-78489653a0fdafbd5401	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Melilotoside 10V, Positive-QTOF	splash10-00mk-0904000000-3dd34e382ba43fc1764f	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Melilotoside 20V, Positive-QTOF	splash10-0arr-0596000000-829180a1d0df8715f61c	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Melilotoside 40V, Positive-QTOF	splash10-014i-2900000000-e9a87fed398fa7e220c1	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Melilotoside 10V, Negative-QTOF	splash10-07f0-0598000000-7c06dab5e1ee09a3e269	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Melilotoside 20V, Negative-QTOF	splash10-0j4i-1931000000-be23d1fceb38e06a6c84	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Melilotoside 40V, Negative-QTOF	splash10-014i-3900000000-c4aef0c58740bba64b21	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

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

FDB030731

KNApSAcK ID

Not Available

Chemspider ID

22912899

KEGG Compound ID

C05839

BioCyc ID

CPD-7417

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5316113

PDB ID

Not Available

ChEBI ID

62251

Food Biomarker Ontology

Not Available

VMH ID

BDG2HC

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Thiele I, Swainston N, Fleming RM, Hoppe A, Sahoo S, Aurich MK, Haraldsdottir H, Mo ML, Rolfsson O, Stobbe MD, Thorleifsson SG, Agren R, Bolling C, Bordel S, Chavali AK, Dobson P, Dunn WB, Endler L, Hala D, Hucka M, Hull D, Jameson D, Jamshidi N, Jonsson JJ, Juty N, Keating S, Nookaew I, Le Novere N, Malys N, Mazein A, Papin JA, Price ND, Selkov E Sr, Sigurdsson MI, Simeonidis E, Sonnenschein N, Smallbone K, Sorokin A, van Beek JH, Weichart D, Goryanin I, Nielsen J, Westerhoff HV, Kell DB, Mendes P, Palsson BO: A community-driven global reconstruction of human metabolism. Nat Biotechnol. 2013 May;31(5):419-25. doi: 10.1038/nbt.2488. Epub 2013 Mar 3. [PubMed:23455439 ]

Enzymes

Enzyme Details

1. Cytosolic beta-glucosidase

General function:: Involved in hydrolase activity, hydrolyzing O-glycosyl compounds
Specific function:: Glycosidase probably involved in the intestinal absorption and metabolism of dietary flavonoid glycosides. Able to hydrolyze a broad variety of glycosides including phytoestrogens, flavonols, flavones, flavanones and cyanogens. Possesses beta-glycosylceramidase activity and may be involved in a nonlysosomal catabolic pathway of glycosylceramide.
Gene Name:: GBA3
Uniprot ID:: Q9H227
Molecular weight:: Not Available

Reactions

cis-Melilotoside + Water → 4-Hydroxycinnamic acid + D-Glucose	details

Showing metabocard for cis-Melilotoside (HMDB0060077)

MOL for HMDB0060077 (cis-Melilotoside)

3D MOL for HMDB0060077 (cis-Melilotoside)

3D SDF for HMDB0060077 (cis-Melilotoside)

3D-SDF for HMDB0060077 (cis-Melilotoside)

PDB for HMDB0060077 (cis-Melilotoside)

3D PDB for HMDB0060077 (cis-Melilotoside)

SMILES for HMDB0060077 (cis-Melilotoside)

INCHI for HMDB0060077 (cis-Melilotoside)

Structure for HMDB0060077 (cis-Melilotoside)

3D Structure for HMDB0060077 (cis-Melilotoside)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions