NP-MRD: Showing NP-Card for 3,9-Dihydroxy-2-geranylcoumestan (NP0057055)

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Record Information

Version

2.0

Created at

2022-04-28 02:36:52 UTC

Updated at

2022-04-28 02:36:52 UTC

NP-MRD ID

NP0057055

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,9-Dihydroxy-2-geranylcoumestan

Description

Puerarol belongs to the class of organic compounds known as coumestans. These are polycyclic aromatic compounds containing a coumestan moiety, which consists of a benzoxole fused to a chromen-2-one to form 1-Benzoxolo[3,2-c]chromen-6-one. They are oxidation products of pterocarpan. Thus, puerarol is considered to be a flavonoid. 3,9-Dihydroxy-2-geranylcoumestan is found in Pueraria lobata , Pueraria montana, Pueraria spp. and Pueraria thunbergiana . Based on a literature review very few articles have been published on Puerarol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282204362D          

 30 33  0  0  0  0            999 V2000
    5.1672    0.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7962    1.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9726    1.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5199    0.4596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8909   -0.2772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7145   -0.3244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4382   -0.9670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6146   -0.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1619   -1.6095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2436   -0.1829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6962    0.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1801    1.1504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4085    0.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4477    0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7537   -0.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0204   -0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0188    0.7906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6753    1.2366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7521    1.1687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2489    1.7920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8779    2.5288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3305    3.2186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1542    3.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9595    3.9554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4122    4.6452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0412    5.3821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4938    6.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1228    6.8087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3175    6.0246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9909    0.3182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
  4 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 10 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 17 19  1  0  0  0  0
  2 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
  1 30  1  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
    5.9675    0.7434    1.5409 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0101    1.6903    0.9442 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4854    2.7749    1.8350 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6304    1.5962   -0.3003 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1067    0.5500   -1.2344 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9347   -0.2379   -1.7881 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1816   -0.9210   -0.6666 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9269   -1.8839    0.1417 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9427   -0.6301   -0.4525 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1068   -1.2081    0.5784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2016   -1.6265   -0.0406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2940   -0.7729    0.1374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4896   -1.0911   -0.4167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6031   -2.2568   -1.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5344   -3.0982   -1.3257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3065   -2.7801   -0.7615 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7773   -3.6605   -0.9538 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7951   -2.5251   -1.6716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8228   -1.7260   -1.5067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9198   -2.0421   -2.0298 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7581   -0.5584   -0.7889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6435    0.4466   -0.4574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9852    0.6403   -0.7499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6251    1.7650   -0.2721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9402    2.7077    0.5002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6438    3.8138    0.9475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6070    2.4859    0.7734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9364    1.3655    0.3075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7181    0.9097    0.4057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5503   -0.2260   -0.2223 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3470   -0.1007    1.9649 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4883    1.2280    2.4315 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7429    0.3688    0.8553 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9506    2.2739    2.6755 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7551    3.3577    1.2774 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2786    3.4342    2.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9141    2.3487   -0.6552 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6356    1.0943   -2.0645 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8431   -0.1438   -0.8328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2489    0.3740   -2.3760 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3526   -1.0139   -2.4510 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4639   -2.0373    1.1109 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0179   -1.6499    0.2088 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9116   -2.8769   -0.3989 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4760    0.1274   -1.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8759   -0.4193    1.3260 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4865   -2.1329    1.0618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1880    0.1372    0.7138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6270   -4.0077   -1.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6796   -3.5021   -0.5664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4743   -0.1136   -1.3496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6621    1.9085   -0.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1441    3.8866    1.8003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0680    3.2141    1.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 16  2  0
 16 17  1  0
 16 15  1  0
 15 14  2  0
 14 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 30  2  0
 30 29  1  0
 29 28  1  0
 28 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 25 27  2  0
 30 13  1  0
 13 12  2  0
 12 11  1  0
 13 14  1  0
 22 21  1  0
 27 28  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  6 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
 10 46  1  0
 10 47  1  0
 17 50  1  0
 15 49  1  0
 23 51  1  0
 24 52  1  0
 26 53  1  0
 27 54  1  0
 12 48  1  0
M  END


  Mrv1652304282204362D          

 30 33  0  0  0  0            999 V2000
    5.1672    0.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7962    1.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9726    1.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5199    0.4596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8909   -0.2772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7145   -0.3244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4382   -0.9670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6146   -0.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1619   -1.6095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2436   -0.1829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6962    0.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1801    1.1504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4085    0.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4477    0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7537   -0.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0204   -0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0188    0.7906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6753    1.2366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7521    1.1687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2489    1.7920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8779    2.5288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3305    3.2186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1542    3.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9595    3.9554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4122    4.6452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0412    5.3821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4938    6.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1228    6.8087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3175    6.0246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9909    0.3182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
  4 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 10 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 17 19  1  0  0  0  0
  2 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
  1 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0057055

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC\C(C)=C\CC1=C(O)C=C2OC(=O)C3=C(OC4=C3C=CC(O)=C4)C2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H24O5/c1-14(2)5-4-6-15(3)7-8-16-11-19-22(13-20(16)27)30-25(28)23-18-10-9-17(26)12-21(18)29-24(19)23/h5,7,9-13,26-27H,4,6,8H2,1-3H3/b15-7+

> <INCHI_KEY>
CGMGCGYLRFAMQF-VIZOYTHASA-N

> <FORMULA>
C25H24O5

> <MOLECULAR_WEIGHT>
404.462

> <EXACT_MASS>
404.162373873

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
45.03117931178631

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-5,14-dihydroxy-8,17-dioxatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1(10),2,4,6,11(16),12,14-heptaen-9-one

> <ALOGPS_LOGP>
5.62

> <JCHEM_LOGP>
5.785602596666667

> <ALOGPS_LOGS>
-4.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.109939979025064

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.9199102585182555

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0537347585619488

> <JCHEM_POLAR_SURFACE_AREA>
79.9

> <JCHEM_REFRACTIVITY>
117.6649

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.84e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-5,14-dihydroxy-8,17-dioxatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1(10),2,4,6,11(16),12,14-heptaen-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       9.645   0.682   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.953   2.057   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.415   2.146   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.570   0.858   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.263  -0.517   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.800  -0.606   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.418  -1.805   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.881  -1.717   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.036  -3.004   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.188  -0.341   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.033   0.946   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.070   2.147   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.629   1.603   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.702   0.064   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.407  -0.768   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.038  -0.063   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.035   1.476   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.260   2.308   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.404   2.181   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.798   3.345   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.105   4.720   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.950   6.008   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.488   5.920   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.258   7.383   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.103   8.671   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.410  10.046   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.255  11.334   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.563  12.709   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.793  11.246   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      11.183   0.594   0.000  0.00  0.00           O+0
CONECT    1    2    6   30                                                  
CONECT    2    1    3   20                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   14                                                  
CONECT   11   10    4   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   10   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17   13                                                       
CONECT   19   17                                                            
CONECT   20    2   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30    1                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₄O₅

Average Mass

404.4620 Da

Monoisotopic Mass

404.16237 Da

IUPAC Name

4-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-5,14-dihydroxy-8,17-dioxatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1(10),2,4,6,11(16),12,14-heptaen-9-one

Traditional Name

4-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-5,14-dihydroxy-8,17-dioxatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1(10),2,4,6,11(16),12,14-heptaen-9-one

CAS Registry Number

Not Available

SMILES

CC(C)=CCC\C(C)=C\CC1=C(O)C=C2OC(=O)C3=C(OC4=C3C=CC(O)=C4)C2=C1

InChI Identifier

InChI=1S/C25H24O5/c1-14(2)5-4-6-15(3)7-8-16-11-19-22(13-20(16)27)30-25(28)23-18-10-9-17(26)12-21(18)29-24(19)23/h5,7,9-13,26-27H,4,6,8H2,1-3H3/b15-7+

InChI Key

CGMGCGYLRFAMQF-VIZOYTHASA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Pueraria lobata	Plant	KNApSAcK
Pueraria montana	LOTUS Database	35616633
Pueraria spp.	Plant	KNApSAcK
Pueraria thunbergiana	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumestans. These are polycyclic aromatic compounds containing a coumestan moiety, which consists of a benzoxole fused to a chromen-2-one to form 1-Benzoxolo[3,2-c]chromen-6-one. They are oxidation products of pterocarpan.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Coumestans

Direct Parent

Coumestans

Alternative Parents

Substituents

Coumestan
Terpene lactone
Angular furanocoumarin
Furanocoumarin
Coumarin
Aromatic monoterpenoid
Benzopyran
1-benzopyran
Monoterpenoid
Benzofuran
Furopyran
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyranone
Pyran
Benzenoid
Furan
Heteroaromatic compound
Lactone
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Coumestan flavonoids (LMPK12090011 )

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	5.62	ALOGPS
logP	5.79	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	6.92	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.9 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	117.66 m³·mol⁻¹	ChemAxon
Polarizability	45.03 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00010061

Chemspider ID

24843106

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44257531

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 3,9-Dihydroxy-2-geranylcoumestan (NP0057055)

MOL for NP0057055 (3,9-Dihydroxy-2-geranylcoumestan)

3D MOL for NP0057055 (3,9-Dihydroxy-2-geranylcoumestan)

3D SDF for NP0057055 (3,9-Dihydroxy-2-geranylcoumestan)

3D-SDF for NP0057055 (3,9-Dihydroxy-2-geranylcoumestan)

PDB for NP0057055 (3,9-Dihydroxy-2-geranylcoumestan)

3D PDB for NP0057055 (3,9-Dihydroxy-2-geranylcoumestan)

SMILES for NP0057055 (3,9-Dihydroxy-2-geranylcoumestan)

INCHI for NP0057055 (3,9-Dihydroxy-2-geranylcoumestan)

Structure for NP0057055 (3,9-Dihydroxy-2-geranylcoumestan)

3D Structure for NP0057055 (3,9-Dihydroxy-2-geranylcoumestan)