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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 18:00:23 UTC

Update Date

2022-03-07 02:53:39 UTC

HMDB ID

HMDB0033292

Secondary Accession Numbers

HMDB33292

Metabolite Identification

Common Name

8-Hydroxy-3,9-dimethoxypterocarpan

Description

8-Hydroxy-3,9-dimethoxypterocarpan belongs to the class of organic compounds known as pterocarpans. These are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids. Thus, 8-hydroxy-3,9-dimethoxypterocarpan is considered to be a flavonoid lipid molecule. 8-Hydroxy-3,9-dimethoxypterocarpan is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Outside of the human body, 8-hydroxy-3,9-dimethoxypterocarpan has been detected, but not quantified in, green vegetables. This could make 8-hydroxy-3,9-dimethoxypterocarpan a potential biomarker for the consumption of these foods.

Structure

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

HMDB0033292
     RDKit          3D
8-Hydroxy-3,9-dimethoxypterocarpan
 38 41  0  0  0  0  0  0  0  0999 V2000
    6.5388    0.5971    1.5155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7499    1.0503    0.4413 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4437    0.6578    0.3466 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8902   -0.1735    1.2860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5533   -0.5644    1.1730 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7718   -0.1278    0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3377    0.7060   -0.8096 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6739    1.0986   -0.6994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5396    1.1355   -1.8536 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1787    0.8038   -2.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1564   -0.5452   -1.4017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6121   -0.5974   -1.1235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6900   -1.0638   -1.8312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9961   -1.0000   -1.3455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0641   -1.4914   -2.1092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1766   -0.4396   -0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4681   -0.3677    0.3990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7723    0.1783    1.6465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0822    0.0247    0.5987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7894   -0.0369    0.1213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5359    0.3595    0.6324 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3916   -0.5406    0.0241 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2232    1.0136    2.4865 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5095   -0.5255    1.5467 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5763    0.9307    1.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5008   -0.5122    2.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1188   -1.2279    1.9267 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0663    1.7615   -1.4740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1255    0.8425   -3.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4744    1.5580   -1.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2124   -1.3910   -1.9916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5927   -1.5165   -2.8241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9788   -1.4077   -1.6858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0352   -0.0893    2.4185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8720    1.3003    1.6145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7925   -0.1766    1.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2481    0.4684    1.5908 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1860   -1.5321    0.5101 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  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
  8  3  1  0
 22 11  1  0
 22  6  1  0
 20 12  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  5 27  1  0
  8 28  1  0
 10 29  1  0
 10 30  1  0
 11 31  1  0
 13 32  1  0
 15 33  1  0
 18 34  1  0
 18 35  1  0
 18 36  1  0
 19 37  1  0
 22 38  1  0
M  END


  Mrv0541 05061307022D          

 22 25  0  0  0  0            999 V2000
    6.8689   -1.1420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2842   -3.5534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3033   -2.6629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4796   -2.7100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2216   -1.2363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2608   -1.1491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1823   -2.7972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1217   -0.6408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6743   -1.9260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0270   -2.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9548   -1.5951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7507   -1.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5275   -1.5272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3980   -1.2834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9156   -2.4191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4883   -2.3512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2033   -2.0674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1666   -1.0812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4979   -1.8789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2450   -2.7293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9453   -0.5937    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6872   -2.7111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  2  0  0  0  0
  9  3  1  0  0  0  0
  9  5  2  0  0  0  0
 10  4  1  0  0  0  0
 11  6  2  0  0  0  0
 12  8  1  0  0  0  0
 12 11  1  0  0  0  0
 13  6  1  0  0  0  0
 14  5  1  0  0  0  0
 14 10  2  0  0  0  0
 15  7  2  0  0  0  0
 15 11  1  0  0  0  0
 16  7  1  0  0  0  0
 16 13  2  0  0  0  0
 17 10  1  0  0  0  0
 17 12  1  0  0  0  0
 18 13  1  0  0  0  0
 19  1  1  0  0  0  0
 19  9  1  0  0  0  0
 20  2  1  0  0  0  0
 20 16  1  0  0  0  0
 21  8  1  0  0  0  0
 21 14  1  0  0  0  0
 22 15  1  0  0  0  0
 22 17  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0033292

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=CC2=C(C=C1)C1OC3=CC(OC)=C(O)C=C3C1CO2

> <INCHI_IDENTIFIER>
InChI=1S/C17H16O5/c1-19-9-3-4-10-14(5-9)21-8-12-11-6-13(18)16(20-2)7-15(11)22-17(10)12/h3-7,12,17-18H,8H2,1-2H3

> <INCHI_KEY>
KIKDCPYSYOMXEJ-UHFFFAOYSA-N

> <FORMULA>
C17H16O5

> <MOLECULAR_WEIGHT>
300.3059

> <EXACT_MASS>
300.099773622

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
31.30954898561751

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,14-dimethoxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaen-13-ol

> <ALOGPS_LOGP>
2.87

> <JCHEM_LOGP>
2.3515521306666667

> <ALOGPS_LOGS>
-3.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.315411672285467

> <JCHEM_PKA_STRONGEST_BASIC>
-4.272189769425692

> <JCHEM_POLAR_SURFACE_AREA>
57.150000000000006

> <JCHEM_REFRACTIVITY>
79.52430000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.88e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,14-dimethoxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaen-13-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0033292
     RDKit          3D
8-Hydroxy-3,9-dimethoxypterocarpan
 38 41  0  0  0  0  0  0  0  0999 V2000
    6.5388    0.5971    1.5155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7499    1.0503    0.4413 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4437    0.6578    0.3466 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8902   -0.1735    1.2860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5533   -0.5644    1.1730 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7718   -0.1278    0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3377    0.7060   -0.8096 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6739    1.0986   -0.6994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5396    1.1355   -1.8536 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1787    0.8038   -2.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1564   -0.5452   -1.4017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6121   -0.5974   -1.1235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6900   -1.0638   -1.8312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9961   -1.0000   -1.3455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0641   -1.4914   -2.1092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1766   -0.4396   -0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4681   -0.3677    0.3990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7723    0.1783    1.6465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0822    0.0247    0.5987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7894   -0.0369    0.1213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5359    0.3595    0.6324 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3916   -0.5406    0.0241 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2232    1.0136    2.4865 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5095   -0.5255    1.5467 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5763    0.9307    1.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5008   -0.5122    2.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1188   -1.2279    1.9267 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0663    1.7615   -1.4740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1255    0.8425   -3.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4744    1.5580   -1.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2124   -1.3910   -1.9916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5927   -1.5165   -2.8241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9788   -1.4077   -1.6858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0352   -0.0893    2.4185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8720    1.3003    1.6145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7925   -0.1766    1.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2481    0.4684    1.5908 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1860   -1.5321    0.5101 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  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
  8  3  1  0
 22 11  1  0
 22  6  1  0
 20 12  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  5 27  1  0
  8 28  1  0
 10 29  1  0
 10 30  1  0
 11 31  1  0
 13 32  1  0
 15 33  1  0
 18 34  1  0
 18 35  1  0
 18 36  1  0
 19 37  1  0
 22 38  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      12.822  -2.132   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.531  -6.633   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.899  -4.971   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.362  -5.059   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.747  -2.308   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.353  -2.145   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.207  -5.221   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.827  -1.196   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.592  -3.595   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.517  -3.771   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.649  -2.978   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.135  -2.572   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.985  -2.851   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.210  -2.396   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.576  -4.516   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.911  -4.389   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.979  -3.859   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.311  -2.018   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      12.129  -3.507   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -0.457  -5.095   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       7.365  -1.108   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       5.016  -5.061   0.000  0.00  0.00           O+0
CONECT    1   19                                                            
CONECT    2   20                                                            
CONECT    3    4    9                                                       
CONECT    4    3   10                                                       
CONECT    5    9   14                                                       
CONECT    6   11   13                                                       
CONECT    7   15   16                                                       
CONECT    8   12   21                                                       
CONECT    9    3    5   19                                                  
CONECT   10    4   14   17                                                  
CONECT   11    6   12   15                                                  
CONECT   12    8   11   17                                                  
CONECT   13    6   16   18                                                  
CONECT   14    5   10   21                                                  
CONECT   15    7   11   22                                                  
CONECT   16    7   13   20                                                  
CONECT   17   10   12   22                                                  
CONECT   18   13                                                            
CONECT   19    1    9                                                       
CONECT   20    2   16                                                       
CONECT   21    8   14                                                       
CONECT   22   15   17                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   50    0
END

COMPND    HMDB0033292
HETATM    1  C1  UNL     1       6.539   0.597   1.516  1.00  0.00           C  
HETATM    2  O1  UNL     1       5.750   1.050   0.441  1.00  0.00           O  
HETATM    3  C2  UNL     1       4.444   0.658   0.347  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.890  -0.174   1.286  1.00  0.00           C  
HETATM    5  C4  UNL     1       2.553  -0.564   1.173  1.00  0.00           C  
HETATM    6  C5  UNL     1       1.772  -0.128   0.127  1.00  0.00           C  
HETATM    7  C6  UNL     1       2.338   0.706  -0.810  1.00  0.00           C  
HETATM    8  C7  UNL     1       3.674   1.099  -0.699  1.00  0.00           C  
HETATM    9  O2  UNL     1       1.540   1.136  -1.854  1.00  0.00           O  
HETATM   10  C8  UNL     1       0.179   0.804  -2.002  1.00  0.00           C  
HETATM   11  C9  UNL     1      -0.156  -0.545  -1.402  1.00  0.00           C  
HETATM   12  C10 UNL     1      -1.612  -0.597  -1.123  1.00  0.00           C  
HETATM   13  C11 UNL     1      -2.690  -1.064  -1.831  1.00  0.00           C  
HETATM   14  C12 UNL     1      -3.996  -1.000  -1.345  1.00  0.00           C  
HETATM   15  O3  UNL     1      -5.064  -1.491  -2.109  1.00  0.00           O  
HETATM   16  C13 UNL     1      -4.177  -0.440  -0.100  1.00  0.00           C  
HETATM   17  O4  UNL     1      -5.468  -0.368   0.399  1.00  0.00           O  
HETATM   18  C14 UNL     1      -5.772   0.178   1.647  1.00  0.00           C  
HETATM   19  C15 UNL     1      -3.082   0.025   0.599  1.00  0.00           C  
HETATM   20  C16 UNL     1      -1.789  -0.037   0.121  1.00  0.00           C  
HETATM   21  O5  UNL     1      -0.536   0.360   0.632  1.00  0.00           O  
HETATM   22  C17 UNL     1       0.392  -0.541   0.024  1.00  0.00           C  
HETATM   23  H1  UNL     1       6.223   1.014   2.487  1.00  0.00           H  
HETATM   24  H2  UNL     1       6.510  -0.526   1.547  1.00  0.00           H  
HETATM   25  H3  UNL     1       7.576   0.931   1.339  1.00  0.00           H  
HETATM   26  H4  UNL     1       4.501  -0.512   2.100  1.00  0.00           H  
HETATM   27  H5  UNL     1       2.119  -1.228   1.927  1.00  0.00           H  
HETATM   28  H6  UNL     1       4.066   1.762  -1.474  1.00  0.00           H  
HETATM   29  H7  UNL     1      -0.126   0.842  -3.072  1.00  0.00           H  
HETATM   30  H8  UNL     1      -0.474   1.558  -1.483  1.00  0.00           H  
HETATM   31  H9  UNL     1       0.212  -1.391  -1.992  1.00  0.00           H  
HETATM   32  H10 UNL     1      -2.593  -1.516  -2.824  1.00  0.00           H  
HETATM   33  H11 UNL     1      -5.979  -1.408  -1.686  1.00  0.00           H  
HETATM   34  H12 UNL     1      -5.035  -0.089   2.419  1.00  0.00           H  
HETATM   35  H13 UNL     1      -5.872   1.300   1.615  1.00  0.00           H  
HETATM   36  H14 UNL     1      -6.792  -0.177   1.962  1.00  0.00           H  
HETATM   37  H15 UNL     1      -3.248   0.468   1.591  1.00  0.00           H  
HETATM   38  H16 UNL     1       0.186  -1.532   0.510  1.00  0.00           H  
CONECT    1    2   23   24   25
CONECT    2    3
CONECT    3    4    4    8
CONECT    4    5   26
CONECT    5    6    6   27
CONECT    6    7   22
CONECT    7    8    8    9
CONECT    8   28
CONECT    9   10
CONECT   10   11   29   30
CONECT   11   12   22   31
CONECT   12   13   13   20
CONECT   13   14   32
CONECT   14   15   16   16
CONECT   15   33
CONECT   16   17   19
CONECT   17   18
CONECT   18   34   35   36
CONECT   19   20   20   37
CONECT   20   21
CONECT   21   22
CONECT   22   38
END

HMDB0033292
     RDKit          3D
8-Hydroxy-3,9-dimethoxypterocarpan
 38 41  0  0  0  0  0  0  0  0999 V2000
    6.5388    0.5971    1.5155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7499    1.0503    0.4413 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4437    0.6578    0.3466 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8902   -0.1735    1.2860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5533   -0.5644    1.1730 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7718   -0.1278    0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3377    0.7060   -0.8096 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6739    1.0986   -0.6994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5396    1.1355   -1.8536 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1787    0.8038   -2.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1564   -0.5452   -1.4017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6121   -0.5974   -1.1235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6900   -1.0638   -1.8312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9961   -1.0000   -1.3455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0641   -1.4914   -2.1092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1766   -0.4396   -0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4681   -0.3677    0.3990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7723    0.1783    1.6465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0822    0.0247    0.5987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7894   -0.0369    0.1213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5359    0.3595    0.6324 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3916   -0.5406    0.0241 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2232    1.0136    2.4865 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5095   -0.5255    1.5467 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5763    0.9307    1.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5008   -0.5122    2.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1188   -1.2279    1.9267 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0663    1.7615   -1.4740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1255    0.8425   -3.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4744    1.5580   -1.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2124   -1.3910   -1.9916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5927   -1.5165   -2.8241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9788   -1.4077   -1.6858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0352   -0.0893    2.4185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8720    1.3003    1.6145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7925   -0.1766    1.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2481    0.4684    1.5908 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1860   -1.5321    0.5101 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  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
  8  3  1  0
 22 11  1  0
 22  6  1  0
 20 12  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  5 27  1  0
  8 28  1  0
 10 29  1  0
 10 30  1  0
 11 31  1  0
 13 32  1  0
 15 33  1  0
 18 34  1  0
 18 35  1  0
 18 36  1  0
 19 37  1  0
 22 38  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(6AR,11ar)-8-hydroxy-3,9-dimethoxypterocarpan	HMDB

Chemical Formula

C₁₇H₁₆O₅

Average Molecular Weight

300.3059

Monoisotopic Molecular Weight

300.099773622

IUPAC Name

5,14-dimethoxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaen-13-ol

Traditional Name

5,14-dimethoxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaen-13-ol

CAS Registry Number

108335-31-5

SMILES

COC1=CC2=C(C=C1)C1OC3=CC(OC)=C(O)C=C3C1CO2

InChI Identifier

InChI=1S/C17H16O5/c1-19-9-3-4-10-14(5-9)21-8-12-11-6-13(18)16(20-2)7-15(11)22-17(10)12/h3-7,12,17-18H,8H2,1-2H3

InChI Key

KIKDCPYSYOMXEJ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pterocarpans. These are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Furanoisoflavonoids

Direct Parent

Pterocarpans

Alternative Parents

Not Available

Substituents

Not Available

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0033292)

Cellular substructure

Membrane (HMDB: HMDB0033292)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0033292)

Source

Endogenous

Plant

Plant (HMDB: HMDB0033292)

Exogenous

Food

Food (HMDB: HMDB0033292)

Vegetable

Leaf vegetable

Green vegetables (FooDB: FOOD00872)

Not Available

Nutrient (HMDB: HMDB0033292)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	129 °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	0.089 g/L	ALOGPS
logP	2.87	ALOGPS
logP	2.35	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	10.32	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	57.15 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	79.52 m³·mol⁻¹	ChemAxon
Polarizability	31.31 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	170.97	31661259
DarkChem	[M-H]-	172.188	31661259
DeepCCS	[M+H]+	175.329	30932474
DeepCCS	[M-H]-	172.972	30932474
DeepCCS	[M-2H]-	205.877	30932474
DeepCCS	[M+Na]+	181.423	30932474
AllCCS	[M+H]+	170.9	32859911
AllCCS	[M+H-H2O]+	167.3	32859911
AllCCS	[M+NH4]+	174.2	32859911
AllCCS	[M+Na]+	175.2	32859911
AllCCS	[M-H]-	175.3	32859911
AllCCS	[M+Na-2H]-	174.7	32859911
AllCCS	[M+HCOO]-	174.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
8-Hydroxy-3,9-dimethoxypterocarpan	COC1=CC2=C(C=C1)C1OC3=CC(OC)=C(O)C=C3C1CO2	3806.9	Standard polar	33892256
8-Hydroxy-3,9-dimethoxypterocarpan	COC1=CC2=C(C=C1)C1OC3=CC(OC)=C(O)C=C3C1CO2	2520.1	Standard non polar	33892256
8-Hydroxy-3,9-dimethoxypterocarpan	COC1=CC2=C(C=C1)C1OC3=CC(OC)=C(O)C=C3C1CO2	2709.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
8-Hydroxy-3,9-dimethoxypterocarpan,1TMS,isomer #1	COC1=CC=C2C(=C1)OCC1C3=CC(O[Si](C)(C)C)=C(OC)C=C3OC21	2729.7	Semi standard non polar	33892256
8-Hydroxy-3,9-dimethoxypterocarpan,1TBDMS,isomer #1	COC1=CC=C2C(=C1)OCC1C3=CC(O[Si](C)(C)C(C)(C)C)=C(OC)C=C3OC21	2988.8	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 - 8-Hydroxy-3,9-dimethoxypterocarpan GC-MS (Non-derivatized) - 70eV, Positive	splash10-0229-0890000000-76dfcd08ccb9327275e2	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan GC-MS (1 TMS) - 70eV, Positive	splash10-0ab9-2329000000-35c2b549957cc4856015	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan 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 - 8-Hydroxy-3,9-dimethoxypterocarpan 10V, Positive-QTOF	splash10-0udi-0019000000-63da12e8b050a75505ca	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan 20V, Positive-QTOF	splash10-0udi-0249000000-470f9309267f1265004f	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan 40V, Positive-QTOF	splash10-0pb9-6960000000-b7337bd9416a18685211	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan 10V, Negative-QTOF	splash10-0002-0090000000-7f2d02992916d44d180d	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan 20V, Negative-QTOF	splash10-0002-0090000000-43aa7e31c85785ac928a	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan 40V, Negative-QTOF	splash10-0udr-1190000000-3c583683043c63d2b068	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan 10V, Negative-QTOF	splash10-0002-0090000000-c8e04b941de97dd002f4	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan 20V, Negative-QTOF	splash10-0002-0090000000-b7824e819e86dc962cb6	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan 40V, Negative-QTOF	splash10-0ldr-1290000000-571e00ca4365ce610ee9	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan 10V, Positive-QTOF	splash10-0udi-0009000000-7fd5921050e52686aed7	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan 20V, Positive-QTOF	splash10-0udi-0219000000-9b6f093db77e957eefc7	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Hydroxy-3,9-dimethoxypterocarpan 40V, Positive-QTOF	splash10-070i-0950000000-468f33b7192f0baf752e	2021-09-25	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

FDB011316

KNApSAcK ID

C00010007

Chemspider ID

400548

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

454891

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.. .

Enzymes

Enzyme Details

1. UDP-glucuronosyltransferase 1-1

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform glucuronidates bilirubin IX-alpha to form both the IX-alpha-C8 and IX-alpha-C12 monoconjugates and diconjugate. Is also able to catalyze the glucuronidation of 17beta-estradiol, 17alpha-ethinylestradiol, 1-hydroxypyrene, 4-methylumbelliferone, 1-naphthol, paranitrophenol, scopoletin, and umbelliferone.
Gene Name:: UGT1A1
Uniprot ID:: P22309
Molecular weight:: 59590.91

Reactions

8-Hydroxy-3,9-dimethoxypterocarpan → 6-({5,14-dimethoxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaen-13-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid	details

Showing metabocard for 8-Hydroxy-3,9-dimethoxypterocarpan (HMDB0033292)

MOL for HMDB0033292 (8-Hydroxy-3,9-dimethoxypterocarpan)

3D MOL for HMDB0033292 (8-Hydroxy-3,9-dimethoxypterocarpan)

3D SDF for HMDB0033292 (8-Hydroxy-3,9-dimethoxypterocarpan)

3D-SDF for HMDB0033292 (8-Hydroxy-3,9-dimethoxypterocarpan)

PDB for HMDB0033292 (8-Hydroxy-3,9-dimethoxypterocarpan)

3D PDB for HMDB0033292 (8-Hydroxy-3,9-dimethoxypterocarpan)

SMILES for HMDB0033292 (8-Hydroxy-3,9-dimethoxypterocarpan)

INCHI for HMDB0033292 (8-Hydroxy-3,9-dimethoxypterocarpan)

Structure for HMDB0033292 (8-Hydroxy-3,9-dimethoxypterocarpan)

3D Structure for HMDB0033292 (8-Hydroxy-3,9-dimethoxypterocarpan)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes

Reactions