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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:19:11 UTC

Update Date

2022-03-07 02:55:10 UTC

HMDB ID

HMDB0037077

Secondary Accession Numbers

HMDB37077

Metabolite Identification

Common Name

(Z)-Resveratrol 3-(6''-sulfoglucopyranoside)

Description

(Z)-Resveratrol 3-(6''-sulfoglucopyranoside) belongs to the class of organic compounds known as stilbene glycosides. Stilbene glycosides are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) has been detected, but not quantified in, green vegetables. This could make (Z)-resveratrol 3-(6''-sulfoglucopyranoside) a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on (Z)-Resveratrol 3-(6''-sulfoglucopyranoside).

Structure

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


  Mrv0541 02241209192D          

 32 34  0  0  0  0            999 V2000
   -2.4022    0.0990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6599   -0.3141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9176    0.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9176    0.8413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6599    1.1703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4022    0.9239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0633    1.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0633    2.1605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4022    2.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6599    2.2431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9176    2.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9176    3.3986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6599    3.8103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4022    3.3986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1754    1.3355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1754    3.8103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6599   -1.1391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6355    0.8677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6355   -0.0679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4448   -0.5356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2524   -0.0679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2524    0.8677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4448    1.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4448   -1.4713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0633   -0.5356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0633    1.3355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4448    2.2697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6355   -1.9390    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6355   -2.8747    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.6355   -3.8103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1754   -3.3425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4464   -3.3425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  2  0  0  0  0
  2  3  2  0  0  0  0
  2 17  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4 15  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 14  2  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 16  1  0  0  0  0
 13 14  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 23  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 24  1  0  0  0  0
 21 22  1  0  0  0  0
 21 25  1  0  0  0  0
 22 23  1  0  0  0  0
 22 26  1  0  0  0  0
 23 27  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 29 32  2  0  0  0  0
M  END

HMDB0037077
     RDKit          3D
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside)
 54 56  0  0  0  0  0  0  0  0999 V2000
    4.9253   -1.7667   -3.4082 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5229   -3.0740   -2.7736 S   0  0  0  0  0  6  0  0  0  0  0  0
    5.7719   -3.7787   -2.3601 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6397   -3.9324   -3.9107 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5279   -2.7445   -1.4358 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9225   -1.5238   -0.9450 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1610   -1.0511    0.2460 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8059   -0.9016    0.0240 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184   -0.0400    0.9993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0093    0.3063    0.8545 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6129    1.4987    0.7010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0901    2.6688    0.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5651    3.8823    0.5041 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1123    5.0878    0.4628 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9286    3.8949    0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6808    2.7173    0.4149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0905    2.8402    0.4409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9503    2.0235   -0.0699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6756    0.8381   -0.7955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6171   -0.1975   -0.7135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5499   -1.3412   -1.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5212   -1.5256   -2.3606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4004   -2.6599   -3.1456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5852   -0.5493   -2.4765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6678    0.6186   -1.6999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0024    1.5426    0.5758 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4966   -0.6193    2.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2311    0.4552    3.2784 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9115   -1.0449    2.6647 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7176    0.0519    2.8880 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3738   -1.8785    1.4825 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6870   -2.3008    1.6265 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1297   -4.0121   -4.7465 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9138   -0.7180   -1.7071 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9927   -1.6254   -0.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5515   -0.0207    0.4890 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9495    0.8672    0.9740 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1655    2.7289    0.7527 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1050    5.1967    0.5413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4465    4.8578    0.2562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5219    3.7592    0.9722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0534    2.2927    0.0801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4487   -0.0890   -0.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2881   -2.1223   -1.3803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8263   -2.7051   -4.0571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7739   -0.6772   -3.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9327    1.3699   -1.8687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5678    0.6260    0.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7620   -1.4219    2.5139 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9877    0.0400    4.1417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8932   -1.6771    3.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0012    0.1492    3.8263 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7237   -2.7547    1.4340 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3255   -1.5603    1.7506 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  2  0
  2  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 16 26  2  0
  9 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31  7  1  0
 26 11  1  0
 25 19  1  0
  4 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  9 37  1  0
 12 38  1  0
 14 39  1  0
 15 40  1  0
 17 41  1  0
 18 42  1  0
 20 43  1  0
 21 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
 26 48  1  0
 27 49  1  0
 28 50  1  0
 29 51  1  0
 30 52  1  0
 31 53  1  0
 32 54  1  0
M  END


  Mrv0541 02241209192D          

 32 34  0  0  0  0            999 V2000
   -2.4022    0.0990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6599   -0.3141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9176    0.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9176    0.8413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6599    1.1703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4022    0.9239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0633    1.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0633    2.1605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4022    2.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6599    2.2431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9176    2.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9176    3.3986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6599    3.8103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4022    3.3986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1754    1.3355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1754    3.8103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6599   -1.1391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6355    0.8677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6355   -0.0679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4448   -0.5356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2524   -0.0679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2524    0.8677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4448    1.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4448   -1.4713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0633   -0.5356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0633    1.3355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4448    2.2697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6355   -1.9390    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6355   -2.8747    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.6355   -3.8103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1754   -3.3425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4464   -3.3425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  2  0  0  0  0
  2  3  2  0  0  0  0
  2 17  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4 15  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 14  2  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 16  1  0  0  0  0
 13 14  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 23  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 24  1  0  0  0  0
 21 22  1  0  0  0  0
 21 25  1  0  0  0  0
 22 23  1  0  0  0  0
 22 26  1  0  0  0  0
 23 27  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 29 32  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037077

> <DATABASE_NAME>
hmdb

> <SMILES>
OC1C(COS(O)(=O)=O)OC(OC2=CC(\C=C/C3=CC=C(O)C=C3)=CC(O)=C2)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H22O11S/c21-13-5-3-11(4-6-13)1-2-12-7-14(22)9-15(8-12)30-20-19(25)18(24)17(23)16(31-20)10-29-32(26,27)28/h1-9,16-25H,10H2,(H,26,27,28)/b2-1-

> <INCHI_KEY>
WOXRJKNGYKAHCY-UPHRSURJSA-N

> <FORMULA>
C20H22O11S

> <MOLECULAR_WEIGHT>
470.447

> <EXACT_MASS>
470.088282236

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
44.41584416092337

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(3,4,5-trihydroxy-6-{3-hydroxy-5-[(Z)-2-(4-hydroxyphenyl)ethenyl]phenoxy}oxan-2-yl)methoxy]sulfonic acid

> <ALOGPS_LOGP>
0.14

> <JCHEM_LOGP>
-0.7109275397490373

> <ALOGPS_LOGS>
-2.32

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.10197935051096

> <JCHEM_PKA_STRONGEST_ACIDIC>
-2.06827413869616

> <JCHEM_PKA_STRONGEST_BASIC>
-3.650124788807651

> <JCHEM_POLAR_SURFACE_AREA>
183.20999999999998

> <JCHEM_REFRACTIVITY>
109.59169999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.25e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3,4,5-trihydroxy-6-{3-hydroxy-5-[(Z)-2-(4-hydroxyphenyl)ethenyl]phenoxy}oxan-2-yl)methoxysulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0037077
     RDKit          3D
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside)
 54 56  0  0  0  0  0  0  0  0999 V2000
    4.9253   -1.7667   -3.4082 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5229   -3.0740   -2.7736 S   0  0  0  0  0  6  0  0  0  0  0  0
    5.7719   -3.7787   -2.3601 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6397   -3.9324   -3.9107 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5279   -2.7445   -1.4358 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9225   -1.5238   -0.9450 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1610   -1.0511    0.2460 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8059   -0.9016    0.0240 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184   -0.0400    0.9993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0093    0.3063    0.8545 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6129    1.4987    0.7010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0901    2.6688    0.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5651    3.8823    0.5041 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1123    5.0878    0.4628 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9286    3.8949    0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6808    2.7173    0.4149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0905    2.8402    0.4409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9503    2.0235   -0.0699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6756    0.8381   -0.7955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6171   -0.1975   -0.7135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5499   -1.3412   -1.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5212   -1.5256   -2.3606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4004   -2.6599   -3.1456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5852   -0.5493   -2.4765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6678    0.6186   -1.6999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0024    1.5426    0.5758 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4966   -0.6193    2.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2311    0.4552    3.2784 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9115   -1.0449    2.6647 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7176    0.0519    2.8880 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3738   -1.8785    1.4825 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6870   -2.3008    1.6265 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1297   -4.0121   -4.7465 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9138   -0.7180   -1.7071 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9927   -1.6254   -0.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5515   -0.0207    0.4890 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9495    0.8672    0.9740 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1655    2.7289    0.7527 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1050    5.1967    0.5413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4465    4.8578    0.2562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5219    3.7592    0.9722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0534    2.2927    0.0801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4487   -0.0890   -0.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2881   -2.1223   -1.3803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8263   -2.7051   -4.0571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7739   -0.6772   -3.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9327    1.3699   -1.8687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5678    0.6260    0.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7620   -1.4219    2.5139 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9877    0.0400    4.1417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8932   -1.6771    3.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0012    0.1492    3.8263 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7237   -2.7547    1.4340 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3255   -1.5603    1.7506 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  2  0
  2  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 16 26  2  0
  9 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31  7  1  0
 26 11  1  0
 25 19  1  0
  4 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  9 37  1  0
 12 38  1  0
 14 39  1  0
 15 40  1  0
 17 41  1  0
 18 42  1  0
 20 43  1  0
 21 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
 26 48  1  0
 27 49  1  0
 28 50  1  0
 29 51  1  0
 30 52  1  0
 31 53  1  0
 32 54  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -4.484   0.185   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.098  -0.586   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.713   0.031   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.713   1.570   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.098   2.185   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.484   1.725   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.718   2.493   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.718   4.033   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.484   4.804   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.098   4.187   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.713   4.804   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.713   6.344   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.098   7.113   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.484   6.344   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -0.327   2.493   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -0.327   7.113   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -3.098  -2.126   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.186   1.620   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.186  -0.127   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.697  -1.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.204  -0.127   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.204   1.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.697   2.493   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.697  -2.746   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.718  -1.000   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       5.718   2.493   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       2.697   4.237   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       1.186  -3.619   0.000  0.00  0.00           O+0
HETATM   29  S   UNK     0       1.186  -5.366   0.000  0.00  0.00           S+0
HETATM   30  O   UNK     0       1.186  -7.113   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -0.327  -6.239   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       2.700  -6.239   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   17                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   15                                                  
CONECT    5    4    6                                                       
CONECT    6    1    5    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14    9   13                                                       
CONECT   15    4   18                                                       
CONECT   16   12                                                            
CONECT   17    2                                                            
CONECT   18   15   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22   25                                                  
CONECT   22   21   23   26                                                  
CONECT   23   18   22   27                                                  
CONECT   24   20   28                                                       
CONECT   25   21                                                            
CONECT   26   22                                                            
CONECT   27   23                                                            
CONECT   28   24   29                                                       
CONECT   29   28   30   31   32                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   29                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

COMPND    HMDB0037077
HETATM    1  O1  UNL     1       4.925  -1.767  -3.408  1.00  0.00           O  
HETATM    2  S1  UNL     1       4.523  -3.074  -2.774  1.00  0.00           S  
HETATM    3  O2  UNL     1       5.772  -3.779  -2.360  1.00  0.00           O  
HETATM    4  O3  UNL     1       3.640  -3.932  -3.911  1.00  0.00           O  
HETATM    5  O4  UNL     1       3.528  -2.744  -1.436  1.00  0.00           O  
HETATM    6  C1  UNL     1       3.923  -1.524  -0.945  1.00  0.00           C  
HETATM    7  C2  UNL     1       3.161  -1.051   0.246  1.00  0.00           C  
HETATM    8  O5  UNL     1       1.806  -0.902   0.024  1.00  0.00           O  
HETATM    9  C3  UNL     1       1.318  -0.040   0.999  1.00  0.00           C  
HETATM   10  O6  UNL     1      -0.009   0.306   0.854  1.00  0.00           O  
HETATM   11  C4  UNL     1      -0.613   1.499   0.701  1.00  0.00           C  
HETATM   12  C5  UNL     1       0.090   2.669   0.664  1.00  0.00           C  
HETATM   13  C6  UNL     1      -0.565   3.882   0.504  1.00  0.00           C  
HETATM   14  O7  UNL     1       0.112   5.088   0.463  1.00  0.00           O  
HETATM   15  C7  UNL     1      -1.929   3.895   0.383  1.00  0.00           C  
HETATM   16  C8  UNL     1      -2.681   2.717   0.415  1.00  0.00           C  
HETATM   17  C9  UNL     1      -4.090   2.840   0.441  1.00  0.00           C  
HETATM   18  C10 UNL     1      -4.950   2.024  -0.070  1.00  0.00           C  
HETATM   19  C11 UNL     1      -4.676   0.838  -0.795  1.00  0.00           C  
HETATM   20  C12 UNL     1      -5.617  -0.198  -0.713  1.00  0.00           C  
HETATM   21  C13 UNL     1      -5.550  -1.341  -1.465  1.00  0.00           C  
HETATM   22  C14 UNL     1      -4.521  -1.526  -2.361  1.00  0.00           C  
HETATM   23  O8  UNL     1      -4.400  -2.660  -3.146  1.00  0.00           O  
HETATM   24  C15 UNL     1      -3.585  -0.549  -2.477  1.00  0.00           C  
HETATM   25  C16 UNL     1      -3.668   0.619  -1.700  1.00  0.00           C  
HETATM   26  C17 UNL     1      -2.002   1.543   0.576  1.00  0.00           C  
HETATM   27  C18 UNL     1       1.497  -0.619   2.405  1.00  0.00           C  
HETATM   28  O9  UNL     1       1.231   0.455   3.278  1.00  0.00           O  
HETATM   29  C19 UNL     1       2.912  -1.045   2.665  1.00  0.00           C  
HETATM   30  O10 UNL     1       3.718   0.052   2.888  1.00  0.00           O  
HETATM   31  C20 UNL     1       3.374  -1.878   1.482  1.00  0.00           C  
HETATM   32  O11 UNL     1       4.687  -2.301   1.626  1.00  0.00           O  
HETATM   33  H1  UNL     1       4.130  -4.012  -4.746  1.00  0.00           H  
HETATM   34  H2  UNL     1       3.914  -0.718  -1.707  1.00  0.00           H  
HETATM   35  H3  UNL     1       4.993  -1.625  -0.634  1.00  0.00           H  
HETATM   36  H4  UNL     1       3.551  -0.021   0.489  1.00  0.00           H  
HETATM   37  H5  UNL     1       1.950   0.867   0.974  1.00  0.00           H  
HETATM   38  H6  UNL     1       1.166   2.729   0.753  1.00  0.00           H  
HETATM   39  H7  UNL     1       1.105   5.197   0.541  1.00  0.00           H  
HETATM   40  H8  UNL     1      -2.446   4.858   0.256  1.00  0.00           H  
HETATM   41  H9  UNL     1      -4.522   3.759   0.972  1.00  0.00           H  
HETATM   42  H10 UNL     1      -6.053   2.293   0.080  1.00  0.00           H  
HETATM   43  H11 UNL     1      -6.449  -0.089  -0.014  1.00  0.00           H  
HETATM   44  H12 UNL     1      -6.288  -2.122  -1.380  1.00  0.00           H  
HETATM   45  H13 UNL     1      -4.826  -2.705  -4.057  1.00  0.00           H  
HETATM   46  H14 UNL     1      -2.774  -0.677  -3.172  1.00  0.00           H  
HETATM   47  H15 UNL     1      -2.933   1.370  -1.869  1.00  0.00           H  
HETATM   48  H16 UNL     1      -2.568   0.626   0.659  1.00  0.00           H  
HETATM   49  H17 UNL     1       0.762  -1.422   2.514  1.00  0.00           H  
HETATM   50  H18 UNL     1       0.988   0.040   4.142  1.00  0.00           H  
HETATM   51  H19 UNL     1       2.893  -1.677   3.585  1.00  0.00           H  
HETATM   52  H20 UNL     1       4.001   0.149   3.826  1.00  0.00           H  
HETATM   53  H21 UNL     1       2.724  -2.755   1.434  1.00  0.00           H  
HETATM   54  H22 UNL     1       5.326  -1.560   1.751  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    3    4    5
CONECT    4   33
CONECT    5    6
CONECT    6    7   34   35
CONECT    7    8   31   36
CONECT    8    9
CONECT    9   10   27   37
CONECT   10   11
CONECT   11   12   12   26
CONECT   12   13   38
CONECT   13   14   15   15
CONECT   14   39
CONECT   15   16   40
CONECT   16   17   26   26
CONECT   17   18   18   41
CONECT   18   19   42
CONECT   19   20   20   25
CONECT   20   21   43
CONECT   21   22   22   44
CONECT   22   23   24
CONECT   23   45
CONECT   24   25   25   46
CONECT   25   47
CONECT   26   48
CONECT   27   28   29   49
CONECT   28   50
CONECT   29   30   31   51
CONECT   30   52
CONECT   31   32   53
CONECT   32   54
END

HMDB0037077
     RDKit          3D
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside)
 54 56  0  0  0  0  0  0  0  0999 V2000
    4.9253   -1.7667   -3.4082 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5229   -3.0740   -2.7736 S   0  0  0  0  0  6  0  0  0  0  0  0
    5.7719   -3.7787   -2.3601 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6397   -3.9324   -3.9107 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5279   -2.7445   -1.4358 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9225   -1.5238   -0.9450 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1610   -1.0511    0.2460 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8059   -0.9016    0.0240 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184   -0.0400    0.9993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0093    0.3063    0.8545 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6129    1.4987    0.7010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0901    2.6688    0.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5651    3.8823    0.5041 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1123    5.0878    0.4628 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9286    3.8949    0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6808    2.7173    0.4149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0905    2.8402    0.4409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9503    2.0235   -0.0699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6756    0.8381   -0.7955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6171   -0.1975   -0.7135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5499   -1.3412   -1.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5212   -1.5256   -2.3606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4004   -2.6599   -3.1456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5852   -0.5493   -2.4765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6678    0.6186   -1.6999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0024    1.5426    0.5758 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4966   -0.6193    2.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2311    0.4552    3.2784 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9115   -1.0449    2.6647 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7176    0.0519    2.8880 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3738   -1.8785    1.4825 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6870   -2.3008    1.6265 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1297   -4.0121   -4.7465 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9138   -0.7180   -1.7071 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9927   -1.6254   -0.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5515   -0.0207    0.4890 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9495    0.8672    0.9740 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1655    2.7289    0.7527 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1050    5.1967    0.5413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4465    4.8578    0.2562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5219    3.7592    0.9722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0534    2.2927    0.0801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4487   -0.0890   -0.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2881   -2.1223   -1.3803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8263   -2.7051   -4.0571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7739   -0.6772   -3.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9327    1.3699   -1.8687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5678    0.6260    0.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7620   -1.4219    2.5139 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9877    0.0400    4.1417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8932   -1.6771    3.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0012    0.1492    3.8263 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7237   -2.7547    1.4340 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3255   -1.5603    1.7506 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  2  0
  2  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 16 26  2  0
  9 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31  7  1  0
 26 11  1  0
 25 19  1  0
  4 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  9 37  1  0
 12 38  1  0
 14 39  1  0
 15 40  1  0
 17 41  1  0
 18 42  1  0
 20 43  1  0
 21 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
 26 48  1  0
 27 49  1  0
 28 50  1  0
 29 51  1  0
 30 52  1  0
 31 53  1  0
 32 54  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
(Z)-Resveratrol 3-(6''-sulphoglucopyranoside)	Generator
[(3,4,5-Trihydroxy-6-{3-hydroxy-5-[(Z)-2-(4-hydroxyphenyl)ethenyl]phenoxy}oxan-2-yl)methoxy]sulfonate	Generator
[(3,4,5-Trihydroxy-6-{3-hydroxy-5-[(Z)-2-(4-hydroxyphenyl)ethenyl]phenoxy}oxan-2-yl)methoxy]sulphonate	Generator
[(3,4,5-Trihydroxy-6-{3-hydroxy-5-[(Z)-2-(4-hydroxyphenyl)ethenyl]phenoxy}oxan-2-yl)methoxy]sulphonic acid	Generator
(e)-Resveratrol 3-(6''-sulphoglucoside)	Generator

Chemical Formula

C₂₀H₂₂O₁₁S

Average Molecular Weight

470.447

Monoisotopic Molecular Weight

470.088282236

IUPAC Name

[(3,4,5-trihydroxy-6-{3-hydroxy-5-[(Z)-2-(4-hydroxyphenyl)ethenyl]phenoxy}oxan-2-yl)methoxy]sulfonic acid

Traditional Name

(3,4,5-trihydroxy-6-{3-hydroxy-5-[(Z)-2-(4-hydroxyphenyl)ethenyl]phenoxy}oxan-2-yl)methoxysulfonic acid

CAS Registry Number

Not Available

SMILES

OC1C(COS(O)(=O)=O)OC(OC2=CC(\C=C/C3=CC=C(O)C=C3)=CC(O)=C2)C(O)C1O

InChI Identifier

InChI=1S/C20H22O11S/c21-13-5-3-11(4-6-13)1-2-12-7-14(22)9-15(8-12)30-20-19(25)18(24)17(23)16(31-20)10-29-32(26,27)28/h1-9,16-25H,10H2,(H,26,27,28)/b2-1-

InChI Key

WOXRJKNGYKAHCY-UPHRSURJSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbene glycosides. Stilbene glycosides are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Stilbene glycosides

Direct Parent

Stilbene glycosides

Alternative Parents

Substituents

Stilbene glycoside
Phenolic glycoside
Glycosyl compound
O-glycosyl compound
Monosaccharide sulfate
Phenoxy compound
Phenol ether
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alkyl sulfate
Sulfuric acid ester
Sulfate-ester
Sulfuric acid monoester
Benzenoid
Oxane
Monosaccharide
Monocyclic benzene moiety
Organic sulfuric acid or derivatives
Secondary alcohol
Organoheterocyclic compound
Acetal
Oxacycle
Polyol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0037077)
Cytoplasm (HMDB: HMDB0037077)

Source

Exogenous

Exogenous (HMDB: HMDB0037077)

Food

Vegetable

Leaf vegetable

Green vegetables (FooDB: FOOD00872)

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	2.25 g/L	ALOGPS
logP	0.14	ALOGPS
logP	-0.71	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	-2.1	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	183.21 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	109.59 m³·mol⁻¹	ChemAxon
Polarizability	44.42 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	217.084	30932474
DeepCCS	[M-H]-	214.689	30932474
DeepCCS	[M-2H]-	247.57	30932474
DeepCCS	[M+Na]+	222.997	30932474
AllCCS	[M+H]+	206.6	32859911
AllCCS	[M+H-H2O]+	204.5	32859911
AllCCS	[M+NH4]+	208.6	32859911
AllCCS	[M+Na]+	209.2	32859911
AllCCS	[M-H]-	199.7	32859911
AllCCS	[M+Na-2H]-	200.5	32859911
AllCCS	[M+HCOO]-	201.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside)	OC1C(COS(O)(=O)=O)OC(OC2=CC(\C=C/C3=CC=C(O)C=C3)=CC(O)=C2)C(O)C1O	8033.3	Standard polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside)	OC1C(COS(O)(=O)=O)OC(OC2=CC(\C=C/C3=CC=C(O)C=C3)=CC(O)=C2)C(O)C1O	4069.6	Standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside)	OC1C(COS(O)(=O)=O)OC(OC2=CC(\C=C/C3=CC=C(O)C=C3)=CC(O)=C2)C(O)C1O	4575.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),1TMS,isomer #1	C[Si](C)(C)OC1C(COS(=O)(=O)O)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O)C1O	4306.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),1TMS,isomer #2	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O)C(O)C3O)=C2)C=C1	4347.8	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),1TMS,isomer #3	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O)C(O)C2O)=C1	4330.9	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),1TMS,isomer #4	C[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)OC(COS(=O)(=O)O)C(O)C1O	4310.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),1TMS,isomer #5	C[Si](C)(C)OC1C(O)C(COS(=O)(=O)O)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C1O	4311.6	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),1TMS,isomer #6	C[Si](C)(C)OS(=O)(=O)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O)C(O)C1O	4342.1	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #1	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O[Si](C)(C)C)C(O)C2O)=C1	4280.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #10	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O)C(O[Si](C)(C)C)C2O)=C1	4287.4	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #11	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O)C(O)C2O[Si](C)(C)C)=C1	4288.9	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #12	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C(O)C2O)=C1	4329.9	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #13	C[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)OC(COS(=O)(=O)O)C(O)C1O[Si](C)(C)C	4307.2	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #14	C[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C1O	4322.8	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #15	C[Si](C)(C)OC1C(O)C(COS(=O)(=O)O[Si](C)(C)C)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C1O	4322.8	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #2	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1	4285.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #3	C[Si](C)(C)OC1C(COS(=O)(=O)O)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O[Si](C)(C)C)C1O	4289.9	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #4	C[Si](C)(C)OC1C(COS(=O)(=O)O)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O)C1O[Si](C)(C)C	4297.2	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #5	C[Si](C)(C)OC1C(COS(=O)(=O)O[Si](C)(C)C)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O)C1O	4314.0	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #6	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1	4312.1	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #7	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1	4286.2	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #8	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1	4298.9	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TMS,isomer #9	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C(O)C3O)=C2)C=C1	4334.3	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #1	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1	4251.9	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #10	C[Si](C)(C)OC1C(COS(=O)(=O)O[Si](C)(C)C)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O)C1O[Si](C)(C)C	4259.4	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #11	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1	4258.4	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #12	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1	4264.8	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #13	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1	4277.6	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #14	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1	4272.9	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #15	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1	4248.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #16	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1	4273.2	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #17	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	4263.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #18	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)=C1	4249.6	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #19	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)=C1	4265.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #2	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=C1	4248.4	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #20	C[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4268.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #3	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=C1	4262.6	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #4	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)=C1	4250.4	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #5	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1	4256.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #6	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1	4270.2	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #7	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1	4259.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #8	C[Si](C)(C)OC1C(COS(=O)(=O)O)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4285.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TMS,isomer #9	C[Si](C)(C)OC1C(COS(=O)(=O)O[Si](C)(C)C)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O[Si](C)(C)C)C1O	4265.3	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #1	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1	4186.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #10	C[Si](C)(C)OC1C(COS(=O)(=O)O[Si](C)(C)C)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4214.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #11	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1	4200.6	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #12	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1	4193.1	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #13	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1	4202.4	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #14	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1	4190.3	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #15	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	4178.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #2	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1	4199.0	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #3	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1	4198.3	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #4	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	4204.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #5	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=C1	4162.6	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #6	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=C1	4191.3	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #7	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1	4213.4	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #8	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1	4178.8	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),4TMS,isomer #9	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1	4199.2	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),5TMS,isomer #1	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1	4165.6	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),5TMS,isomer #2	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1	4161.1	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),5TMS,isomer #3	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1	4175.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),5TMS,isomer #4	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	4139.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),5TMS,isomer #5	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1	4162.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),5TMS,isomer #6	C[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1	4161.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1C(COS(=O)(=O)O)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O)C1O	4566.1	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O)C(O)C3O)=C2)C=C1	4619.2	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O)C(O)C2O)=C1	4590.3	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)OC(COS(=O)(=O)O)C(O)C1O	4581.9	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(O)C(COS(=O)(=O)O)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C1O	4585.6	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OS(=O)(=O)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O)C(O)C1O	4590.6	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=C1	4757.3	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=C1	4781.1	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=C1	4777.1	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)=C1	4795.2	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)OC(COS(=O)(=O)O)C(O)C1O[Si](C)(C)C(C)(C)C	4786.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)OC(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)C(O)C1O	4800.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1C(O)C(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C1O	4798.6	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1	4778.3	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1C(COS(=O)(=O)O)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O[Si](C)(C)C(C)(C)C)C1O	4772.2	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1C(COS(=O)(=O)O)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O)C1O[Si](C)(C)C(C)(C)C	4767.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O)C1O	4774.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1	4823.3	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1	4803.3	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1	4801.8	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=C2)C=C1	4816.3	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1	4937.2	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1C(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O)C1O[Si](C)(C)C(C)(C)C	4878.4	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1	4958.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1	4945.1	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1	4991.4	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1	4907.1	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1	4931.2	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1	4942.0	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)=C1	4886.0	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=C1	4902.1	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=C1	4916.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)=C1	4866.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)OC(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4898.4	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)=C1	4871.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(O)C=C2)=CC(OC2OC(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=C1	4890.1	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1	4887.2	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1	4890.7	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC=C(/C=C\C2=CC(O)=CC(OC3OC(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1	4921.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1C(COS(=O)(=O)O)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4851.5	Semi standard non polar	33892256
(Z)-Resveratrol 3-(6''-sulfoglucopyranoside),3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1C(COS(=O)(=O)O[Si](C)(C)C(C)(C)C)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(O)C=C3)=C2)C(O[Si](C)(C)C(C)(C)C)C1O	4885.2	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 - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) GC-MS (Non-derivatized) - 70eV, Positive	splash10-0h09-4971400000-bc48cd4dfdcaf6f3e46f	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) GC-MS (3 TMS) - 70eV, Positive	splash10-00di-4431019000-d850afdd91be344b3e83	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 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 - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 10V, Positive-QTOF	splash10-004i-0191500000-59926bd47307cf9caef4	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 20V, Positive-QTOF	splash10-004i-0291000000-8bbe7deb18e7de3d5f74	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 40V, Positive-QTOF	splash10-01ta-1960000000-2cba6c30703927bbf463	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 10V, Negative-QTOF	splash10-016r-1190800000-906ec518403c411ce9b0	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 20V, Negative-QTOF	splash10-004i-2190100000-2df79690d825db585101	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 40V, Negative-QTOF	splash10-004i-4490000000-e41639ddeb938cdd9298	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 10V, Negative-QTOF	splash10-004i-0090300000-a8fab171de81a8b2f181	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 20V, Negative-QTOF	splash10-004i-0290000000-bb3e15551e85d561eb3e	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 40V, Negative-QTOF	splash10-0002-9440000000-61c853c5af1e31e265da	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 10V, Positive-QTOF	splash10-00b9-0090400000-73d95dd304db3ea4bf04	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 20V, Positive-QTOF	splash10-004i-0592000000-d3401e9ebe59e7f83521	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) 40V, Positive-QTOF	splash10-0059-4790100000-9000fac5cc5e682c07c9	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

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

FDB016061

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131752142

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for (Z)-Resveratrol 3-(6''-sulfoglucopyranoside) (HMDB0037077)

MOL for HMDB0037077 ((Z)-Resveratrol 3-(6''-sulfoglucopyranoside))

3D MOL for HMDB0037077 ((Z)-Resveratrol 3-(6''-sulfoglucopyranoside))

3D SDF for HMDB0037077 ((Z)-Resveratrol 3-(6''-sulfoglucopyranoside))

3D-SDF for HMDB0037077 ((Z)-Resveratrol 3-(6''-sulfoglucopyranoside))

PDB for HMDB0037077 ((Z)-Resveratrol 3-(6''-sulfoglucopyranoside))

3D PDB for HMDB0037077 ((Z)-Resveratrol 3-(6''-sulfoglucopyranoside))

SMILES for HMDB0037077 ((Z)-Resveratrol 3-(6''-sulfoglucopyranoside))

INCHI for HMDB0037077 ((Z)-Resveratrol 3-(6''-sulfoglucopyranoside))

Structure for HMDB0037077 ((Z)-Resveratrol 3-(6''-sulfoglucopyranoside))

3D Structure for HMDB0037077 ((Z)-Resveratrol 3-(6''-sulfoglucopyranoside))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra