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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:54:09 UTC

Update Date

2022-03-07 02:56:12 UTC

HMDB ID

HMDB0039438

Secondary Accession Numbers

HMDB39438

Metabolite Identification

Common Name

2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid

Description

2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid has been detected, but not quantified in, pulses. This could make 2-hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid.

Structure

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

  Mrv0541 05061311092D          

 25 26  0  0  0  0            999 V2000
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  2  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  6  2  0  0  0  0
 11 10  2  0  0  0  0
 12  9  1  0  0  0  0
 14  1  1  0  0  0  0
 14  2  1  0  0  0  0
 14  9  2  0  0  0  0
 15  7  2  0  0  0  0
 15  8  1  0  0  0  0
 15 10  1  0  0  0  0
 16 11  1  0  0  0  0
 16 13  2  0  0  0  0
 17 12  1  0  0  0  0
 18 13  1  0  0  0  0
 18 17  2  0  0  0  0
 19 16  1  0  0  0  0
 20 17  1  0  0  0  0
 20 19  2  0  0  0  0
 21 19  1  0  0  0  0
 22 20  1  0  0  0  0
 23 21  2  0  0  0  0
 24 21  1  0  0  0  0
 25  3  1  0  0  0  0
 25 18  1  0  0  0  0
M  END

HMDB0039438
     RDKit          3D
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid
 47 48  0  0  0  0  0  0  0  0999 V2000
   -1.8554   -0.4174    2.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3269   -0.4610    1.5895 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3790   -0.3969    0.5739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0406   -0.2941    0.8509 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9286   -0.2280   -0.2050 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2929   -0.1421    0.2220 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3256    0.4713   -0.2733 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6746    0.4449    0.2915 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6692    1.1431   -0.3571 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9832    1.1992    0.0735 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3078    0.5147    1.2169 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3450   -0.1944    1.8943 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0299   -0.2302    1.4335 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4732   -0.2788   -1.4864 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3392   -0.3685   -2.6409 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5650   -0.3175   -2.7197 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7178   -0.5466   -3.9215 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9293   -0.3822   -1.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3684   -0.4240   -3.0332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8458   -0.4407   -0.7112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2621   -0.5494   -1.0169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1708   -0.7643    0.0986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1214    0.1062    0.3838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0662   -0.1169    1.5444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3255    1.3521   -0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7020   -0.4173    3.6414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2614   -1.3436    3.1655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1744    0.4260    3.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3153   -0.2602    1.8564 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5376   -0.7132    1.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1892    1.1293   -1.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4803    1.7128   -1.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7382    1.7599   -0.4635 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3182    0.5103    1.6194 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6273   -0.7265    2.7945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -0.7935    1.9911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0586   -1.2829   -4.5139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3480   -0.4959   -3.2153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3692   -1.4655   -1.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5181    0.3526   -1.6356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0762   -1.6507    0.7002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2659   -1.1902    1.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5595    0.3544    2.4091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0254    0.3827    1.3111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3133    1.8061   -0.1796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5617    2.0661   -0.1056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3667    1.1612   -1.5091 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  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  2  0
  5 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 14 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  2  3
 23 24  1  0
 23 25  1  0
 20  3  1  0
 13  8  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  6 30  1  0
  7 31  1  0
  9 32  1  0
 10 33  1  0
 11 34  1  0
 12 35  1  0
 13 36  1  0
 17 37  1  0
 19 38  1  0
 21 39  1  0
 21 40  1  0
 22 41  1  0
 24 42  1  0
 24 43  1  0
 24 44  1  0
 25 45  1  0
 25 46  1  0
 25 47  1  0
M  END

  Mrv0541 05061311092D          

 25 26  0  0  0  0            999 V2000
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  2  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  6  2  0  0  0  0
 11 10  2  0  0  0  0
 12  9  1  0  0  0  0
 14  1  1  0  0  0  0
 14  2  1  0  0  0  0
 14  9  2  0  0  0  0
 15  7  2  0  0  0  0
 15  8  1  0  0  0  0
 15 10  1  0  0  0  0
 16 11  1  0  0  0  0
 16 13  2  0  0  0  0
 17 12  1  0  0  0  0
 18 13  1  0  0  0  0
 18 17  2  0  0  0  0
 19 16  1  0  0  0  0
 20 17  1  0  0  0  0
 20 19  2  0  0  0  0
 21 19  1  0  0  0  0
 22 20  1  0  0  0  0
 23 21  2  0  0  0  0
 24 21  1  0  0  0  0
 25  3  1  0  0  0  0
 25 18  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0039438

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=C(CC=C(C)C)C(O)=C(C(O)=O)C(\C=C\C2=CC=CC=C2)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O4/c1-14(2)9-12-17-18(25-3)13-16(19(20(17)22)21(23)24)11-10-15-7-5-4-6-8-15/h4-11,13,22H,12H2,1-3H3,(H,23,24)/b11-10+

> <INCHI_KEY>
XPDYDSQPCFQSLH-ZHACJKMWSA-N

> <FORMULA>
C21H22O4

> <MOLECULAR_WEIGHT>
338.397

> <EXACT_MASS>
338.151809192

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
38.10937794664018

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-hydroxy-4-methoxy-3-(3-methylbut-2-en-1-yl)-6-[(E)-2-phenylethenyl]benzoic acid

> <ALOGPS_LOGP>
4.86

> <JCHEM_LOGP>
5.888000171333334

> <ALOGPS_LOGS>
-4.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.127860277229281

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.7788212089747244

> <JCHEM_PKA_STRONGEST_BASIC>
-4.868970018799766

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
101.45589999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.74e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-hydroxy-4-methoxy-3-(3-methylbut-2-en-1-yl)-6-[(E)-2-phenylethenyl]benzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0039438
     RDKit          3D
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid
 47 48  0  0  0  0  0  0  0  0999 V2000
   -1.8554   -0.4174    2.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3269   -0.4610    1.5895 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3790   -0.3969    0.5739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0406   -0.2941    0.8509 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9286   -0.2280   -0.2050 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2929   -0.1421    0.2220 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3256    0.4713   -0.2733 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6746    0.4449    0.2915 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6692    1.1431   -0.3571 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9832    1.1992    0.0735 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3078    0.5147    1.2169 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3450   -0.1944    1.8943 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0299   -0.2302    1.4335 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4732   -0.2788   -1.4864 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3392   -0.3685   -2.6409 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5650   -0.3175   -2.7197 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7178   -0.5466   -3.9215 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9293   -0.3822   -1.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3684   -0.4240   -3.0332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8458   -0.4407   -0.7112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2621   -0.5494   -1.0169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1708   -0.7643    0.0986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1214    0.1062    0.3838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0662   -0.1169    1.5444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3255    1.3521   -0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7020   -0.4173    3.6414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2614   -1.3436    3.1655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1744    0.4260    3.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3153   -0.2602    1.8564 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5376   -0.7132    1.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1892    1.1293   -1.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4803    1.7128   -1.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7382    1.7599   -0.4635 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3182    0.5103    1.6194 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6273   -0.7265    2.7945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -0.7935    1.9911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0586   -1.2829   -4.5139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3480   -0.4959   -3.2153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3692   -1.4655   -1.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5181    0.3526   -1.6356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0762   -1.6507    0.7002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2659   -1.1902    1.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5595    0.3544    2.4091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0254    0.3827    1.3111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3133    1.8061   -0.1796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5617    2.0661   -0.1056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3667    1.1612   -1.5091 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  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  2  0
  5 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 14 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  2  3
 23 24  1  0
 23 25  1  0
 20  3  1  0
 13  8  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  6 30  1  0
  7 31  1  0
  9 32  1  0
 10 33  1  0
 11 34  1  0
 12 35  1  0
 13 36  1  0
 17 37  1  0
 19 38  1  0
 21 39  1  0
 21 40  1  0
 22 41  1  0
 24 42  1  0
 24 43  1  0
 24 44  1  0
 25 45  1  0
 25 46  1  0
 25 47  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1   14                                                            
CONECT    2   14                                                            
CONECT    3   25                                                            
CONECT    4    5    6                                                       
CONECT    5    4    7                                                       
CONECT    6    4    8                                                       
CONECT    7    5   15                                                       
CONECT    8    6   15                                                       
CONECT    9   12   14                                                       
CONECT   10   11   15                                                       
CONECT   11   10   16                                                       
CONECT   12    9   17                                                       
CONECT   13   16   18                                                       
CONECT   14    1    2    9                                                  
CONECT   15    7    8   10                                                  
CONECT   16   11   13   19                                                  
CONECT   17   12   18   20                                                  
CONECT   18   13   17   25                                                  
CONECT   19   16   20   21                                                  
CONECT   20   17   19   22                                                  
CONECT   21   19   23   24                                                  
CONECT   22   20                                                            
CONECT   23   21                                                            
CONECT   24   21                                                            
CONECT   25    3   18                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

COMPND    HMDB0039438
HETATM    1  C1  UNL     1      -1.855  -0.417   2.922  1.00  0.00           C  
HETATM    2  O1  UNL     1      -2.327  -0.461   1.590  1.00  0.00           O  
HETATM    3  C2  UNL     1      -1.379  -0.397   0.574  1.00  0.00           C  
HETATM    4  C3  UNL     1      -0.041  -0.294   0.851  1.00  0.00           C  
HETATM    5  C4  UNL     1       0.929  -0.228  -0.205  1.00  0.00           C  
HETATM    6  C5  UNL     1       2.293  -0.142   0.222  1.00  0.00           C  
HETATM    7  C6  UNL     1       3.326   0.471  -0.273  1.00  0.00           C  
HETATM    8  C7  UNL     1       4.675   0.445   0.292  1.00  0.00           C  
HETATM    9  C8  UNL     1       5.669   1.143  -0.357  1.00  0.00           C  
HETATM   10  C9  UNL     1       6.983   1.199   0.073  1.00  0.00           C  
HETATM   11  C10 UNL     1       7.308   0.515   1.217  1.00  0.00           C  
HETATM   12  C11 UNL     1       6.345  -0.194   1.894  1.00  0.00           C  
HETATM   13  C12 UNL     1       5.030  -0.230   1.434  1.00  0.00           C  
HETATM   14  C13 UNL     1       0.473  -0.279  -1.486  1.00  0.00           C  
HETATM   15  C14 UNL     1       1.339  -0.369  -2.641  1.00  0.00           C  
HETATM   16  O2  UNL     1       2.565  -0.317  -2.720  1.00  0.00           O  
HETATM   17  O3  UNL     1       0.718  -0.547  -3.922  1.00  0.00           O  
HETATM   18  C15 UNL     1      -0.929  -0.382  -1.719  1.00  0.00           C  
HETATM   19  O4  UNL     1      -1.368  -0.424  -3.033  1.00  0.00           O  
HETATM   20  C16 UNL     1      -1.846  -0.441  -0.711  1.00  0.00           C  
HETATM   21  C17 UNL     1      -3.262  -0.549  -1.017  1.00  0.00           C  
HETATM   22  C18 UNL     1      -4.171  -0.764   0.099  1.00  0.00           C  
HETATM   23  C19 UNL     1      -5.121   0.106   0.384  1.00  0.00           C  
HETATM   24  C20 UNL     1      -6.066  -0.117   1.544  1.00  0.00           C  
HETATM   25  C21 UNL     1      -5.326   1.352  -0.412  1.00  0.00           C  
HETATM   26  H1  UNL     1      -2.702  -0.417   3.641  1.00  0.00           H  
HETATM   27  H2  UNL     1      -1.261  -1.344   3.165  1.00  0.00           H  
HETATM   28  H3  UNL     1      -1.174   0.426   3.104  1.00  0.00           H  
HETATM   29  H4  UNL     1       0.315  -0.260   1.856  1.00  0.00           H  
HETATM   30  H5  UNL     1       2.538  -0.713   1.158  1.00  0.00           H  
HETATM   31  H6  UNL     1       3.189   1.129  -1.118  1.00  0.00           H  
HETATM   32  H7  UNL     1       5.480   1.713  -1.279  1.00  0.00           H  
HETATM   33  H8  UNL     1       7.738   1.760  -0.464  1.00  0.00           H  
HETATM   34  H9  UNL     1       8.318   0.510   1.619  1.00  0.00           H  
HETATM   35  H10 UNL     1       6.627  -0.726   2.795  1.00  0.00           H  
HETATM   36  H11 UNL     1       4.316  -0.793   1.991  1.00  0.00           H  
HETATM   37  H12 UNL     1       1.059  -1.283  -4.514  1.00  0.00           H  
HETATM   38  H13 UNL     1      -2.348  -0.496  -3.215  1.00  0.00           H  
HETATM   39  H14 UNL     1      -3.369  -1.465  -1.681  1.00  0.00           H  
HETATM   40  H15 UNL     1      -3.518   0.353  -1.636  1.00  0.00           H  
HETATM   41  H16 UNL     1      -4.076  -1.651   0.700  1.00  0.00           H  
HETATM   42  H17 UNL     1      -6.266  -1.190   1.684  1.00  0.00           H  
HETATM   43  H18 UNL     1      -5.559   0.354   2.409  1.00  0.00           H  
HETATM   44  H19 UNL     1      -7.025   0.383   1.311  1.00  0.00           H  
HETATM   45  H20 UNL     1      -6.313   1.806  -0.180  1.00  0.00           H  
HETATM   46  H21 UNL     1      -4.562   2.066  -0.106  1.00  0.00           H  
HETATM   47  H22 UNL     1      -5.367   1.161  -1.509  1.00  0.00           H  
CONECT    1    2   26   27   28
CONECT    2    3
CONECT    3    4    4   20
CONECT    4    5   29
CONECT    5    6   14   14
CONECT    6    7    7   30
CONECT    7    8   31
CONECT    8    9    9   13
CONECT    9   10   32
CONECT   10   11   11   33
CONECT   11   12   34
CONECT   12   13   13   35
CONECT   13   36
CONECT   14   15   18
CONECT   15   16   16   17
CONECT   17   37
CONECT   18   19   20   20
CONECT   19   38
CONECT   20   21
CONECT   21   22   39   40
CONECT   22   23   23   41
CONECT   23   24   25
CONECT   24   42   43   44
CONECT   25   45   46   47
END

HMDB0039438
     RDKit          3D
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid
 47 48  0  0  0  0  0  0  0  0999 V2000
   -1.8554   -0.4174    2.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3269   -0.4610    1.5895 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3790   -0.3969    0.5739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0406   -0.2941    0.8509 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9286   -0.2280   -0.2050 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2929   -0.1421    0.2220 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3256    0.4713   -0.2733 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6746    0.4449    0.2915 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6692    1.1431   -0.3571 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9832    1.1992    0.0735 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3078    0.5147    1.2169 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3450   -0.1944    1.8943 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0299   -0.2302    1.4335 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4732   -0.2788   -1.4864 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3392   -0.3685   -2.6409 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5650   -0.3175   -2.7197 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7178   -0.5466   -3.9215 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9293   -0.3822   -1.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3684   -0.4240   -3.0332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8458   -0.4407   -0.7112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2621   -0.5494   -1.0169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1708   -0.7643    0.0986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1214    0.1062    0.3838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0662   -0.1169    1.5444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3255    1.3521   -0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7020   -0.4173    3.6414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2614   -1.3436    3.1655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1744    0.4260    3.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3153   -0.2602    1.8564 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5376   -0.7132    1.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1892    1.1293   -1.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4803    1.7128   -1.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7382    1.7599   -0.4635 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3182    0.5103    1.6194 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6273   -0.7265    2.7945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -0.7935    1.9911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0586   -1.2829   -4.5139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3480   -0.4959   -3.2153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3692   -1.4655   -1.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5181    0.3526   -1.6356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0762   -1.6507    0.7002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2659   -1.1902    1.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5595    0.3544    2.4091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0254    0.3827    1.3111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3133    1.8061   -0.1796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5617    2.0661   -0.1056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3667    1.1612   -1.5091 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  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  2  0
  5 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 14 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  2  3
 23 24  1  0
 23 25  1  0
 20  3  1  0
 13  8  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  6 30  1  0
  7 31  1  0
  9 32  1  0
 10 33  1  0
 11 34  1  0
 12 35  1  0
 13 36  1  0
 17 37  1  0
 19 38  1  0
 21 39  1  0
 21 40  1  0
 22 41  1  0
 24 42  1  0
 24 43  1  0
 24 44  1  0
 25 45  1  0
 25 46  1  0
 25 47  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoate	Generator
2-Hydroxy-4-methoxy-3-prenyl-6-styrylbenzoic acid	HMDB
3-Hydroxy-4-prenyl-5-methoxystilbene-2-carboxylic acid	MeSH, HMDB
2-Hydroxy-4-methoxy-3-(3-methylbut-2-en-1-yl)-6-(2-phenylethenyl)benzoate	Generator
Cajaninstilbene acid	MeSH
Cajanin stilbene acid	MeSH

Chemical Formula

C₂₁H₂₂O₄

Average Molecular Weight

338.397

Monoisotopic Molecular Weight

338.151809192

IUPAC Name

2-hydroxy-4-methoxy-3-(3-methylbut-2-en-1-yl)-6-[(E)-2-phenylethenyl]benzoic acid

Traditional Name

2-hydroxy-4-methoxy-3-(3-methylbut-2-en-1-yl)-6-[(E)-2-phenylethenyl]benzoic acid

CAS Registry Number

87402-84-4

SMILES

COC1=C(CC=C(C)C)C(O)=C(C(O)=O)C(\C=C\C2=CC=CC=C2)=C1

InChI Identifier

InChI=1S/C21H22O4/c1-14(2)9-12-17-18(25-3)13-16(19(20(17)22)21(23)24)11-10-15-7-5-4-6-8-15/h4-11,13,22H,12H2,1-3H3,(H,23,24)/b11-10+

InChI Key

XPDYDSQPCFQSLH-ZHACJKMWSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Not Available

Direct Parent

Stilbenes

Alternative Parents

Substituents

Stilbene
P-methoxybenzoic acid or derivatives
Methoxyphenol
Hydroxybenzoic acid
Salicylic acid or derivatives
Salicylic acid
Benzoic acid or derivatives
Benzoic acid
Phenoxy compound
Phenol ether
Anisole
Styrene
Benzoyl
Methoxybenzene
1-hydroxy-4-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Ether
Carboxylic acid
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Membrane (HMDB: HMDB0039438)
Cell membrane (HMDB: HMDB0039438)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0039438)

Source

Exogenous

Exogenous (HMDB: HMDB0039438)

Food

Food (HMDB: HMDB0039438)

Pulse

Pulses (FooDB: FOOD00867)

Endogenous

Plant

Plant (HMDB: HMDB0039438)
Fabaceae (HMDB: HMDB0039438)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0039438)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	150 - 165 °C	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	0.0057 g/L	ALOGPS
logP	4.86	ALOGPS
logP	5.89	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	2.78	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	101.46 m³·mol⁻¹	ChemAxon
Polarizability	38.11 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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
DeepCCS	[M+H]+	190.376	30932474
DeepCCS	[M-H]-	188.018	30932474
DeepCCS	[M-2H]-	222.097	30932474
DeepCCS	[M+Na]+	197.94	30932474
AllCCS	[M+H]+	183.6	32859911
AllCCS	[M+H-H2O]+	180.3	32859911
AllCCS	[M+NH4]+	186.7	32859911
AllCCS	[M+Na]+	187.6	32859911
AllCCS	[M-H]-	182.2	32859911
AllCCS	[M+Na-2H]-	181.9	32859911
AllCCS	[M+HCOO]-	181.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid	COC1=C(CC=C(C)C)C(O)=C(C(O)=O)C(\C=C\C2=CC=CC=C2)=C1	4482.0	Standard polar	33892256
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid	COC1=C(CC=C(C)C)C(O)=C(C(O)=O)C(\C=C\C2=CC=CC=C2)=C1	2763.4	Standard non polar	33892256
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid	COC1=C(CC=C(C)C)C(O)=C(C(O)=O)C(\C=C\C2=CC=CC=C2)=C1	3000.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid,1TMS,isomer #1	COC1=CC(/C=C/C2=CC=CC=C2)=C(C(=O)O)C(O[Si](C)(C)C)=C1CC=C(C)C	2896.8	Semi standard non polar	33892256
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid,1TMS,isomer #2	COC1=CC(/C=C/C2=CC=CC=C2)=C(C(=O)O[Si](C)(C)C)C(O)=C1CC=C(C)C	2870.7	Semi standard non polar	33892256
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid,2TMS,isomer #1	COC1=CC(/C=C/C2=CC=CC=C2)=C(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CC=C(C)C	2864.6	Semi standard non polar	33892256
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid,1TBDMS,isomer #1	COC1=CC(/C=C/C2=CC=CC=C2)=C(C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1CC=C(C)C	3133.7	Semi standard non polar	33892256
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid,1TBDMS,isomer #2	COC1=CC(/C=C/C2=CC=CC=C2)=C(C(=O)O[Si](C)(C)C(C)(C)C)C(O)=C1CC=C(C)C	3131.6	Semi standard non polar	33892256
2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid,2TBDMS,isomer #1	COC1=CC(/C=C/C2=CC=CC=C2)=C(C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CC=C(C)C	3311.5	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 - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-00di-4098000000-3ac92ad0aab178b2b473	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid GC-MS (2 TMS) - 70eV, Positive	splash10-014i-3003900000-6d20ee4b1e3aaf61258e	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 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 - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 10V, Positive-QTOF	splash10-000i-1069000000-0b403f54da111688db60	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 20V, Positive-QTOF	splash10-00ko-2092000000-46d91f6b7cd2c211893d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 40V, Positive-QTOF	splash10-00n3-6590000000-72c6b57e3b7e52e9a105	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 10V, Negative-QTOF	splash10-000l-0069000000-b6f91b20a299d63e0774	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 20V, Negative-QTOF	splash10-002f-0092000000-fdc0f5b4629ae345d4a9	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 40V, Negative-QTOF	splash10-004i-2290000000-40c4bd75b055a512e072	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 10V, Positive-QTOF	splash10-000i-0069000000-e0b2806799ee568cbc40	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 20V, Positive-QTOF	splash10-000i-0091000000-bd957e8e412a2fd490fe	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 40V, Positive-QTOF	splash10-0019-2190000000-1c8af0de348179cbd003	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 10V, Negative-QTOF	splash10-00ku-0069000000-9911b81ad7f8ccae2a2f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 20V, Negative-QTOF	splash10-01pc-0095000000-dbca26ac2cc8af27acfd	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid 40V, Negative-QTOF	splash10-01rl-3293000000-5623447a0a35466ce830	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane

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

FDB019034

KNApSAcK ID

C00054331

Chemspider ID

7994974

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9819225

PDB ID

Not Available

ChEBI ID

174548

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 2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid (HMDB0039438)

MOL for HMDB0039438 (2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid)

3D MOL for HMDB0039438 (2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid)

3D SDF for HMDB0039438 (2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid)

3D-SDF for HMDB0039438 (2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid)

PDB for HMDB0039438 (2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid)

3D PDB for HMDB0039438 (2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid)

SMILES for HMDB0039438 (2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid)

INCHI for HMDB0039438 (2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid)

Structure for HMDB0039438 (2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid)

3D Structure for HMDB0039438 (2-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-6-(2-phenylethenyl)benzoic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra