NP-MRD: Showing NP-Card for 6,4'-dimethoxy-7,2'-dihydroxyisoflavone (NP0031883)

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Record Information

Version

2.0

Created at

2021-06-19 22:50:09 UTC

Updated at

2021-06-30 00:00:44 UTC

NP-MRD ID

NP0031883

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6,4'-dimethoxy-7,2'-dihydroxyisoflavone

Provided By

JEOL Database JEOL Logo

Description

7-Hydroxy-3-(2-hydroxy-4-methoxyphenyl)-6-methoxy-4H-chromen-4-one is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. 6,4'-dimethoxy-7,2'-dihydroxyisoflavone is found in Dalea spinosa. 6,4'-dimethoxy-7,2'-dihydroxyisoflavone was first documented in 2006 (Belofsky, G., et al.). Based on a literature review very few articles have been published on 7-hydroxy-3-(2-hydroxy-4-methoxyphenyl)-6-methoxy-4H-chromen-4-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202100503D          

 37 39  0  0  0  0            999 V2000
   -4.0748   -4.5979   -4.6244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0122   -4.2743   -3.2405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5753   -3.0185   -2.9221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5399   -2.7404   -1.5563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1228   -1.4878   -1.0916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7290   -0.4749   -1.9839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3508    0.8550   -1.4492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0996    1.4584   -0.5104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8667    2.6763    0.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7373    3.3587   -0.2855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4835    4.5675    0.3547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3489    5.2901    0.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1172    6.4759    0.6455 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5432    4.8363   -0.9786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6127    5.6606   -1.2135 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5366    5.2389   -2.2118 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2816    3.6250   -1.6161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8610    2.8909   -1.2622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1610    1.6114   -1.9276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4634    1.2083   -2.8544 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7366   -0.7910   -3.3528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3288    0.0877   -4.3218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1709   -2.0361   -3.8212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7755   -3.9425   -5.1522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4484   -5.6228   -4.7110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0806   -4.5663   -5.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8435   -3.5049   -0.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1103   -1.3208   -0.0164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0111    1.0387   -0.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1573    4.9464    1.1170 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7113    6.8215    0.2587 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0528    5.1674   -3.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3212    5.9984   -2.2821 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0122    4.2926   -1.9338 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9390    3.2285   -2.3835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5125    0.5224   -3.9894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1669   -2.2046   -4.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0  0  0  0
 17 14  1  0  0  0  0
 14 15  1  0  0  0  0
 18 17  2  0  0  0  0
 15 16  1  0  0  0  0
 14 12  2  0  0  0  0
 19 20  2  0  0  0  0
  7  6  1  0  0  0  0
 12 11  1  0  0  0  0
  6  5  2  0  0  0  0
 11 10  2  0  0  0  0
  5  4  1  0  0  0  0
 10  9  1  0  0  0  0
  4  3  2  0  0  0  0
 18 19  1  0  0  0  0
  3 23  1  0  0  0  0
 19  7  1  0  0  0  0
 23 21  2  0  0  0  0
 21  6  1  0  0  0  0
  7  8  2  0  0  0  0
 21 22  1  0  0  0  0
  8  9  1  0  0  0  0
  3  2  1  0  0  0  0
 10 18  1  0  0  0  0
  2  1  1  0  0  0  0
 17 35  1  0  0  0  0
 11 30  1  0  0  0  0
  8 29  1  0  0  0  0
 13 31  1  0  0  0  0
 16 32  1  0  0  0  0
 16 33  1  0  0  0  0
 16 34  1  0  0  0  0
  5 28  1  0  0  0  0
  4 27  1  0  0  0  0
 23 37  1  0  0  0  0
 22 36  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
M  END

     RDKit          3D

 37 39  0  0  0  0  0  0  0  0999 V2000
   -4.0748   -4.5979   -4.6244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0122   -4.2743   -3.2405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5753   -3.0185   -2.9221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5399   -2.7404   -1.5563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1228   -1.4878   -1.0916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7290   -0.4749   -1.9839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3508    0.8550   -1.4492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0996    1.4584   -0.5104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8667    2.6763    0.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7373    3.3587   -0.2855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4835    4.5675    0.3547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3489    5.2901    0.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1172    6.4759    0.6455 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5432    4.8363   -0.9786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6127    5.6606   -1.2135 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5366    5.2389   -2.2118 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2816    3.6250   -1.6161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8610    2.8909   -1.2622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1610    1.6114   -1.9276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4634    1.2083   -2.8544 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7366   -0.7910   -3.3528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3288    0.0877   -4.3218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1709   -2.0361   -3.8212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7755   -3.9425   -5.1522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4484   -5.6228   -4.7110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0806   -4.5663   -5.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8435   -3.5049   -0.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1103   -1.3208   -0.0164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0111    1.0387   -0.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1573    4.9464    1.1170 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7113    6.8215    0.2587 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0528    5.1674   -3.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3212    5.9984   -2.2821 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0122    4.2926   -1.9338 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9390    3.2285   -2.3835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5125    0.5224   -3.9894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1669   -2.2046   -4.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0
 17 14  1  0
 14 15  1  0
 18 17  2  0
 15 16  1  0
 14 12  2  0
 19 20  2  0
  7  6  1  0
 12 11  1  0
  6  5  2  0
 11 10  2  0
  5  4  1  0
 10  9  1  0
  4  3  2  0
 18 19  1  0
  3 23  1  0
 19  7  1  0
 23 21  2  0
 21  6  1  0
  7  8  2  0
 21 22  1  0
  8  9  1  0
  3  2  1  0
 10 18  1  0
  2  1  1  0
 17 35  1  0
 11 30  1  0
  8 29  1  0
 13 31  1  0
 16 32  1  0
 16 33  1  0
 16 34  1  0
  5 28  1  0
  4 27  1  0
 23 37  1  0
 22 36  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
M  END


  Mrv1652306202100503D          

 37 39  0  0  0  0            999 V2000
   -4.0748   -4.5979   -4.6244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0122   -4.2743   -3.2405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5753   -3.0185   -2.9221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5399   -2.7404   -1.5563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1228   -1.4878   -1.0916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7290   -0.4749   -1.9839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3508    0.8550   -1.4492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0996    1.4584   -0.5104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8667    2.6763    0.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7373    3.3587   -0.2855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4835    4.5675    0.3547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3489    5.2901    0.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1172    6.4759    0.6455 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5432    4.8363   -0.9786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6127    5.6606   -1.2135 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5366    5.2389   -2.2118 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2816    3.6250   -1.6161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8610    2.8909   -1.2622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1610    1.6114   -1.9276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4634    1.2083   -2.8544 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7366   -0.7910   -3.3528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3288    0.0877   -4.3218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1709   -2.0361   -3.8212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7755   -3.9425   -5.1522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4484   -5.6228   -4.7110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0806   -4.5663   -5.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8435   -3.5049   -0.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1103   -1.3208   -0.0164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0111    1.0387   -0.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1573    4.9464    1.1170 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7113    6.8215    0.2587 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0528    5.1674   -3.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3212    5.9984   -2.2821 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0122    4.2926   -1.9338 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9390    3.2285   -2.3835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5125    0.5224   -3.9894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1669   -2.2046   -4.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0  0  0  0
 17 14  1  0  0  0  0
 14 15  1  0  0  0  0
 18 17  2  0  0  0  0
 15 16  1  0  0  0  0
 14 12  2  0  0  0  0
 19 20  2  0  0  0  0
  7  6  1  0  0  0  0
 12 11  1  0  0  0  0
  6  5  2  0  0  0  0
 11 10  2  0  0  0  0
  5  4  1  0  0  0  0
 10  9  1  0  0  0  0
  4  3  2  0  0  0  0
 18 19  1  0  0  0  0
  3 23  1  0  0  0  0
 19  7  1  0  0  0  0
 23 21  2  0  0  0  0
 21  6  1  0  0  0  0
  7  8  2  0  0  0  0
 21 22  1  0  0  0  0
  8  9  1  0  0  0  0
  3  2  1  0  0  0  0
 10 18  1  0  0  0  0
  2  1  1  0  0  0  0
 17 35  1  0  0  0  0
 11 30  1  0  0  0  0
  8 29  1  0  0  0  0
 13 31  1  0  0  0  0
 16 32  1  0  0  0  0
 16 33  1  0  0  0  0
 16 34  1  0  0  0  0
  5 28  1  0  0  0  0
  4 27  1  0  0  0  0
 23 37  1  0  0  0  0
 22 36  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0031883

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1C1=C([H])OC2=C([H])C(O[H])=C(OC([H])([H])[H])C([H])=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H14O6/c1-21-9-3-4-10(13(18)5-9)12-8-23-15-7-14(19)16(22-2)6-11(15)17(12)20/h3-8,18-19H,1-2H3

> <INCHI_KEY>
RHNVSRHYVGNPEO-UHFFFAOYSA-N

> <FORMULA>
C17H14O6

> <MOLECULAR_WEIGHT>
314.293

> <EXACT_MASS>
314.079038171

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
32.363674428914884

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-hydroxy-3-(2-hydroxy-4-methoxyphenyl)-6-methoxy-4H-chromen-4-one

> <ALOGPS_LOGP>
3.26

> <JCHEM_LOGP>
2.41509518

> <ALOGPS_LOGS>
-3.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.591087965222119

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.908981768007708

> <JCHEM_PKA_STRONGEST_BASIC>
-4.493520768911794

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
82.62839999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.07e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-hydroxy-3-(2-hydroxy-4-methoxyphenyl)-6-methoxychromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 37 39  0  0  0  0  0  0  0  0999 V2000
   -4.0748   -4.5979   -4.6244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0122   -4.2743   -3.2405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5753   -3.0185   -2.9221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5399   -2.7404   -1.5563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1228   -1.4878   -1.0916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7290   -0.4749   -1.9839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3508    0.8550   -1.4492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0996    1.4584   -0.5104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8667    2.6763    0.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7373    3.3587   -0.2855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4835    4.5675    0.3547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3489    5.2901    0.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1172    6.4759    0.6455 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5432    4.8363   -0.9786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6127    5.6606   -1.2135 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5366    5.2389   -2.2118 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2816    3.6250   -1.6161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8610    2.8909   -1.2622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1610    1.6114   -1.9276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4634    1.2083   -2.8544 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7366   -0.7910   -3.3528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3288    0.0877   -4.3218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1709   -2.0361   -3.8212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7755   -3.9425   -5.1522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4484   -5.6228   -4.7110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0806   -4.5663   -5.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8435   -3.5049   -0.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1103   -1.3208   -0.0164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0111    1.0387   -0.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1573    4.9464    1.1170 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7113    6.8215    0.2587 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0528    5.1674   -3.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3212    5.9984   -2.2821 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0122    4.2926   -1.9338 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9390    3.2285   -2.3835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5125    0.5224   -3.9894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1669   -2.2046   -4.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0
 17 14  1  0
 14 15  1  0
 18 17  2  0
 15 16  1  0
 14 12  2  0
 19 20  2  0
  7  6  1  0
 12 11  1  0
  6  5  2  0
 11 10  2  0
  5  4  1  0
 10  9  1  0
  4  3  2  0
 18 19  1  0
  3 23  1  0
 19  7  1  0
 23 21  2  0
 21  6  1  0
  7  8  2  0
 21 22  1  0
  8  9  1  0
  3  2  1  0
 10 18  1  0
  2  1  1  0
 17 35  1  0
 11 30  1  0
  8 29  1  0
 13 31  1  0
 16 32  1  0
 16 33  1  0
 16 34  1  0
  5 28  1  0
  4 27  1  0
 23 37  1  0
 22 36  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -4.075  -4.598  -4.624  0.00  0.00           C+0
HETATM    2  O   UNK     0      -4.012  -4.274  -3.240  0.00  0.00           O+0
HETATM    3  C   UNK     0      -3.575  -3.018  -2.922  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.540  -2.740  -1.556  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.123  -1.488  -1.092  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.729  -0.475  -1.984  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.351   0.855  -1.449  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.100   1.458  -0.510  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.867   2.676   0.082  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.737   3.359  -0.286  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.484   4.567   0.355  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.349   5.290   0.003  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.117   6.476   0.646  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.543   4.836  -0.979  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.613   5.661  -1.214  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.537   5.239  -2.212  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.282   3.625  -1.616  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.861   2.891  -1.262  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.161   1.611  -1.928  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.463   1.208  -2.854  0.00  0.00           O+0
HETATM   21  C   UNK     0      -2.737  -0.791  -3.353  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.329   0.088  -4.322  0.00  0.00           O+0
HETATM   23  C   UNK     0      -3.171  -2.036  -3.821  0.00  0.00           C+0
HETATM   24  H   UNK     0      -4.776  -3.942  -5.152  0.00  0.00           H+0
HETATM   25  H   UNK     0      -4.448  -5.623  -4.711  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.081  -4.566  -5.082  0.00  0.00           H+0
HETATM   27  H   UNK     0      -3.844  -3.505  -0.845  0.00  0.00           H+0
HETATM   28  H   UNK     0      -3.110  -1.321  -0.016  0.00  0.00           H+0
HETATM   29  H   UNK     0      -4.011   1.039  -0.100  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.157   4.946   1.117  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.711   6.822   0.259  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.053   5.167  -3.192  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.321   5.998  -2.282  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.012   4.293  -1.934  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.939   3.228  -2.384  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.513   0.522  -3.989  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.167  -2.205  -4.893  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    3    1                                                       
CONECT    3    4   23    2                                                  
CONECT    4    5    3   27                                                  
CONECT    5    6    4   28                                                  
CONECT    6    7    5   21                                                  
CONECT    7    6   19    8                                                  
CONECT    8    7    9   29                                                  
CONECT    9   10    8                                                       
CONECT   10   11    9   18                                                  
CONECT   11   12   10   30                                                  
CONECT   12   13   14   11                                                  
CONECT   13   12   31                                                       
CONECT   14   17   15   12                                                  
CONECT   15   14   16                                                       
CONECT   16   15   32   33   34                                             
CONECT   17   14   18   35                                                  
CONECT   18   17   19   10                                                  
CONECT   19   20   18    7                                                  
CONECT   20   19                                                            
CONECT   21   23    6   22                                                  
CONECT   22   21   36                                                       
CONECT   23    3   21   37                                                  
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    4                                                            
CONECT   28    5                                                            
CONECT   29    8                                                            
CONECT   30   11                                                            
CONECT   31   13                                                            
CONECT   32   16                                                            
CONECT   33   16                                                            
CONECT   34   16                                                            
CONECT   35   17                                                            
CONECT   36   22                                                            
CONECT   37   23                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   78    0
END

RDKit          3D

37 39  0  0  0  0  0  0  0  0999 V2000
   -4.0748   -4.5979   -4.6244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0122   -4.2743   -3.2405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5753   -3.0185   -2.9221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5399   -2.7404   -1.5563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1228   -1.4878   -1.0916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7290   -0.4749   -1.9839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3508    0.8550   -1.4492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0996    1.4584   -0.5104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8667    2.6763    0.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7373    3.3587   -0.2855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4835    4.5675    0.3547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3489    5.2901    0.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1172    6.4759    0.6455 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5432    4.8363   -0.9786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6127    5.6606   -1.2135 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5366    5.2389   -2.2118 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2816    3.6250   -1.6161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8610    2.8909   -1.2622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1610    1.6114   -1.9276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4634    1.2083   -2.8544 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7366   -0.7910   -3.3528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3288    0.0877   -4.3218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1709   -2.0361   -3.8212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7755   -3.9425   -5.1522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4484   -5.6228   -4.7110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0806   -4.5663   -5.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8435   -3.5049   -0.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1103   -1.3208   -0.0164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0111    1.0387   -0.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1573    4.9464    1.1170 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7113    6.8215    0.2587 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0528    5.1674   -3.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3212    5.9984   -2.2821 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0122    4.2926   -1.9338 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9390    3.2285   -2.3835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5125    0.5224   -3.9894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1669   -2.2046   -4.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0
 17 14  1  0
 14 15  1  0
 18 17  2  0
 15 16  1  0
 14 12  2  0
 19 20  2  0
  7  6  1  0
 12 11  1  0
  6  5  2  0
 11 10  2  0
  5  4  1  0
 10  9  1  0
  4  3  2  0
 18 19  1  0
  3 23  1  0
 19  7  1  0
 23 21  2  0
 21  6  1  0
  7  8  2  0
 21 22  1  0
  8  9  1  0
  3  2  1  0
 10 18  1  0
  2  1  1  0
 17 35  1  0
 11 30  1  0
  8 29  1  0
 13 31  1  0
 16 32  1  0
 16 33  1  0
 16 34  1  0
  5 28  1  0
  4 27  1  0
 23 37  1  0
 22 36  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₇H₁₄O₆

Average Mass

314.2930 Da

Monoisotopic Mass

314.07904 Da

IUPAC Name

7-hydroxy-3-(2-hydroxy-4-methoxyphenyl)-6-methoxy-4H-chromen-4-one

Traditional Name

7-hydroxy-3-(2-hydroxy-4-methoxyphenyl)-6-methoxychromen-4-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1C1=C([H])OC2=C([H])C(O[H])=C(OC([H])([H])[H])C([H])=C2C1=O

InChI Identifier

InChI=1S/C17H14O6/c1-21-9-3-4-10(13(18)5-9)12-8-23-15-7-14(19)16(22-2)6-11(15)17(12)20/h3-8,18-19H,1-2H3

InChI Key

RHNVSRHYVGNPEO-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Glycyrrhiza pallidiflora	KNApSAcK Database	22123792
Psorothamnus spinosus	JEOL database	Belofsky, G., et al, J. Nat. Prod. 69, 261 (2006)

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as 4'-o-methylisoflavones. These are isoflavones with methoxy groups attached to the C4' atom of the isoflavone backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

O-methylated isoflavonoids

Direct Parent

4'-O-methylisoflavones

Alternative Parents

Substituents

4p-o-methylisoflavone
Isoflavone
Hydroxyisoflavonoid
Chromone
Methoxyphenol
1-benzopyran
Benzopyran
Phenoxy compound
Anisole
Phenol ether
Methoxybenzene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Pyranone
Pyran
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Oxacycle
Organoheterocyclic compound
Ether
Organic oxygen compound
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Isoflavonoids (LMPK12050128 )

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	3.26	ALOGPS
logP	2.42	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	6.91	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	82.63 m³·mol⁻¹	ChemAxon
Polarizability	32.36 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00009851

Chemspider ID

24716692

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Belofsky, G., et al. (2006). Belofsky, G., et al, J. Nat. Prod. 69, 261 (2006). J. Nat. Prod..

Showing NP-Card for 6,4'-dimethoxy-7,2'-dihydroxyisoflavone (NP0031883)

MOL for NP0031883 (6,4'-dimethoxy-7,2'-dihydroxyisoflavone)

3D MOL for NP0031883 (6,4'-dimethoxy-7,2'-dihydroxyisoflavone)

3D SDF for NP0031883 (6,4'-dimethoxy-7,2'-dihydroxyisoflavone)

3D-SDF for NP0031883 (6,4'-dimethoxy-7,2'-dihydroxyisoflavone)

PDB for NP0031883 (6,4'-dimethoxy-7,2'-dihydroxyisoflavone)

3D PDB for NP0031883 (6,4'-dimethoxy-7,2'-dihydroxyisoflavone)

SMILES for NP0031883 (6,4'-dimethoxy-7,2'-dihydroxyisoflavone)

INCHI for NP0031883 (6,4'-dimethoxy-7,2'-dihydroxyisoflavone)

Structure for NP0031883 (6,4'-dimethoxy-7,2'-dihydroxyisoflavone)

3D Structure for NP0031883 (6,4'-dimethoxy-7,2'-dihydroxyisoflavone)