NP-MRD: Showing NP-Card for 7-O-methyl-8-methoxydaidzein (NP0031192)

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Record Information

Version

2.0

Created at

2021-06-19 22:20:47 UTC

Updated at

2021-06-29 23:59:37 UTC

NP-MRD ID

NP0031192

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-O-methyl-8-methoxydaidzein

Provided By

JEOL Database JEOL Logo

Description

SCHEMBL10655498 belongs to the class of organic compounds known as 7-o-methylisoflavones. These are isoflavones with methoxy groups attached to the C7 atom of the isoflavone backbone. 7-O-methyl-8-methoxydaidzein is found in Nocardia species. 7-O-methyl-8-methoxydaidzein was first documented in 2005 (Maatooq, G. T., et al.). Based on a literature review very few articles have been published on SCHEMBL10655498.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202100203D          

 36 38  0  0  0  0            999 V2000
    0.8064   -0.1969    5.1678 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132   -0.3869    3.7930 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0711   -0.3564    2.9038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2450   -0.0135    3.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2405   -0.0251    2.2456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9250   -0.3836    0.9308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9717   -0.4085   -0.1073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1289   -0.1164    0.1723 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5443   -0.7978   -1.4809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4875   -0.8791   -2.6128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7119   -1.5505   -2.4735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6098   -1.6358   -3.5421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2838   -1.0457   -4.7574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1288   -1.1032   -5.8253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0807   -0.3717   -4.9190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1856   -0.2854   -3.8496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2486   -1.1076   -1.6447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2668   -1.0853   -0.6850 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6205   -0.7218    0.5901 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3779   -0.6904    1.5719 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6555   -1.0694    1.2283 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4500    0.0829    0.9488 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4388    0.8179    5.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7324   -0.3225    5.7372 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0926   -0.9475    5.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5327    0.2666    4.2370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2625    0.2413    2.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9822   -2.0103   -1.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5502   -2.1592   -3.4019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9356   -1.5719   -5.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8416    0.0915   -5.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2565    0.2614   -3.9926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8171   -1.4301   -2.5853 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4366   -0.2623    0.6254 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0168    0.6765    0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5857    0.7037    1.8404 H   0  0  0  0  0  0  0  0  0  0  0  0
 19  6  1  0  0  0  0
  7  8  2  0  0  0  0
  5  4  1  0  0  0  0
  9 10  1  0  0  0  0
  6  5  2  0  0  0  0
 10 11  2  0  0  0  0
  4  3  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3 20  1  0  0  0  0
 13 15  1  0  0  0  0
 20 19  2  0  0  0  0
 15 16  2  0  0  0  0
 16 10  1  0  0  0  0
 19 18  1  0  0  0  0
  3  2  1  0  0  0  0
  6  7  1  0  0  0  0
 13 14  1  0  0  0  0
  7  9  1  0  0  0  0
  2  1  1  0  0  0  0
  9 17  2  0  0  0  0
 20 21  1  0  0  0  0
 17 18  1  0  0  0  0
 21 22  1  0  0  0  0
  5 27  1  0  0  0  0
  4 26  1  0  0  0  0
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 14 30  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
 22 34  1  0  0  0  0
 22 35  1  0  0  0  0
 22 36  1  0  0  0  0
M  END

     RDKit          3D

 36 38  0  0  0  0  0  0  0  0999 V2000
    0.8064   -0.1969    5.1678 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132   -0.3869    3.7930 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0711   -0.3564    2.9038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2450   -0.0135    3.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2405   -0.0251    2.2456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9250   -0.3836    0.9308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9717   -0.4085   -0.1073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1289   -0.1164    0.1723 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5443   -0.7978   -1.4809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4875   -0.8791   -2.6128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7119   -1.5505   -2.4735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6098   -1.6358   -3.5421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2838   -1.0457   -4.7574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1288   -1.1032   -5.8253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0807   -0.3717   -4.9190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1856   -0.2854   -3.8496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2486   -1.1076   -1.6447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2668   -1.0853   -0.6850 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6205   -0.7218    0.5901 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3779   -0.6904    1.5719 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6555   -1.0694    1.2283 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4500    0.0829    0.9488 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4388    0.8179    5.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7324   -0.3225    5.7372 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0926   -0.9475    5.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5327    0.2666    4.2370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2625    0.2413    2.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9822   -2.0103   -1.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5502   -2.1592   -3.4019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9356   -1.5719   -5.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8416    0.0915   -5.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2565    0.2614   -3.9926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8171   -1.4301   -2.5853 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4366   -0.2623    0.6254 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0168    0.6765    0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5857    0.7037    1.8404 H   0  0  0  0  0  0  0  0  0  0  0  0
 19  6  1  0
  7  8  2  0
  5  4  1  0
  9 10  1  0
  6  5  2  0
 10 11  2  0
  4  3  2  0
 11 12  1  0
 12 13  2  0
  3 20  1  0
 13 15  1  0
 20 19  2  0
 15 16  2  0
 16 10  1  0
 19 18  1  0
  3  2  1  0
  6  7  1  0
 13 14  1  0
  7  9  1  0
  2  1  1  0
  9 17  2  0
 20 21  1  0
 17 18  1  0
 21 22  1  0
  5 27  1  0
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 17 33  1  0
 11 28  1  0
 12 29  1  0
 15 31  1  0
 16 32  1  0
 14 30  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 22 34  1  0
 22 35  1  0
 22 36  1  0
M  END


  Mrv1652306202100203D          

 36 38  0  0  0  0            999 V2000
    0.8064   -0.1969    5.1678 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132   -0.3869    3.7930 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0711   -0.3564    2.9038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2450   -0.0135    3.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2405   -0.0251    2.2456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9250   -0.3836    0.9308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9717   -0.4085   -0.1073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1289   -0.1164    0.1723 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5443   -0.7978   -1.4809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4875   -0.8791   -2.6128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7119   -1.5505   -2.4735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6098   -1.6358   -3.5421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2838   -1.0457   -4.7574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1288   -1.1032   -5.8253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0807   -0.3717   -4.9190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1856   -0.2854   -3.8496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2486   -1.1076   -1.6447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2668   -1.0853   -0.6850 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6205   -0.7218    0.5901 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3779   -0.6904    1.5719 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6555   -1.0694    1.2283 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4500    0.0829    0.9488 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4388    0.8179    5.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7324   -0.3225    5.7372 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0926   -0.9475    5.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5327    0.2666    4.2370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2625    0.2413    2.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9822   -2.0103   -1.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5502   -2.1592   -3.4019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9356   -1.5719   -5.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8416    0.0915   -5.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2565    0.2614   -3.9926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8171   -1.4301   -2.5853 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4366   -0.2623    0.6254 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0168    0.6765    0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5857    0.7037    1.8404 H   0  0  0  0  0  0  0  0  0  0  0  0
 19  6  1  0  0  0  0
  7  8  2  0  0  0  0
  5  4  1  0  0  0  0
  9 10  1  0  0  0  0
  6  5  2  0  0  0  0
 10 11  2  0  0  0  0
  4  3  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3 20  1  0  0  0  0
 13 15  1  0  0  0  0
 20 19  2  0  0  0  0
 15 16  2  0  0  0  0
 16 10  1  0  0  0  0
 19 18  1  0  0  0  0
  3  2  1  0  0  0  0
  6  7  1  0  0  0  0
 13 14  1  0  0  0  0
  7  9  1  0  0  0  0
  2  1  1  0  0  0  0
  9 17  2  0  0  0  0
 20 21  1  0  0  0  0
 17 18  1  0  0  0  0
 21 22  1  0  0  0  0
  5 27  1  0  0  0  0
  4 26  1  0  0  0  0
 17 33  1  0  0  0  0
 11 28  1  0  0  0  0
 12 29  1  0  0  0  0
 15 31  1  0  0  0  0
 16 32  1  0  0  0  0
 14 30  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
 22 34  1  0  0  0  0
 22 35  1  0  0  0  0
 22 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0031192

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(C([H])=C1[H])C1=C([H])OC2=C(OC([H])([H])[H])C(OC([H])([H])[H])=C([H])C([H])=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H14O5/c1-20-14-8-7-12-15(19)13(9-22-16(12)17(14)21-2)10-3-5-11(18)6-4-10/h3-9,18H,1-2H3

> <INCHI_KEY>
KIVAMNZIYINHSO-UHFFFAOYSA-N

> <FORMULA>
C17H14O5

> <MOLECULAR_WEIGHT>
298.294

> <EXACT_MASS>
298.084123551

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
31.222521860705616

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(4-hydroxyphenyl)-7,8-dimethoxy-4H-chromen-4-one

> <ALOGPS_LOGP>
3.45

> <JCHEM_LOGP>
2.7186605016666663

> <ALOGPS_LOGS>
-3.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.96250685817005

> <JCHEM_PKA_STRONGEST_BASIC>
-4.572479753713042

> <JCHEM_POLAR_SURFACE_AREA>
64.99000000000001

> <JCHEM_REFRACTIVITY>
80.64750000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.28e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(4-hydroxyphenyl)-7,8-dimethoxychromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 36 38  0  0  0  0  0  0  0  0999 V2000
    0.8064   -0.1969    5.1678 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132   -0.3869    3.7930 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0711   -0.3564    2.9038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2450   -0.0135    3.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2405   -0.0251    2.2456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9250   -0.3836    0.9308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9717   -0.4085   -0.1073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1289   -0.1164    0.1723 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5443   -0.7978   -1.4809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4875   -0.8791   -2.6128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7119   -1.5505   -2.4735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6098   -1.6358   -3.5421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2838   -1.0457   -4.7574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1288   -1.1032   -5.8253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0807   -0.3717   -4.9190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1856   -0.2854   -3.8496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2486   -1.1076   -1.6447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2668   -1.0853   -0.6850 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6205   -0.7218    0.5901 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3779   -0.6904    1.5719 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6555   -1.0694    1.2283 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4500    0.0829    0.9488 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4388    0.8179    5.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7324   -0.3225    5.7372 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0926   -0.9475    5.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5327    0.2666    4.2370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2625    0.2413    2.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9822   -2.0103   -1.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5502   -2.1592   -3.4019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9356   -1.5719   -5.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8416    0.0915   -5.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2565    0.2614   -3.9926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8171   -1.4301   -2.5853 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4366   -0.2623    0.6254 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0168    0.6765    0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5857    0.7037    1.8404 H   0  0  0  0  0  0  0  0  0  0  0  0
 19  6  1  0
  7  8  2  0
  5  4  1  0
  9 10  1  0
  6  5  2  0
 10 11  2  0
  4  3  2  0
 11 12  1  0
 12 13  2  0
  3 20  1  0
 13 15  1  0
 20 19  2  0
 15 16  2  0
 16 10  1  0
 19 18  1  0
  3  2  1  0
  6  7  1  0
 13 14  1  0
  7  9  1  0
  2  1  1  0
  9 17  2  0
 20 21  1  0
 17 18  1  0
 21 22  1  0
  5 27  1  0
  4 26  1  0
 17 33  1  0
 11 28  1  0
 12 29  1  0
 15 31  1  0
 16 32  1  0
 14 30  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 22 34  1  0
 22 35  1  0
 22 36  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       0.806  -0.197   5.168  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.113  -0.387   3.793  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.071  -0.356   2.904  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.245  -0.014   3.228  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.240  -0.025   2.246  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.925  -0.384   0.931  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.972  -0.409  -0.107  0.00  0.00           C+0
HETATM    8  O   UNK     0      -4.129  -0.116   0.172  0.00  0.00           O+0
HETATM    9  C   UNK     0      -2.544  -0.798  -1.481  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.487  -0.879  -2.613  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.712  -1.551  -2.474  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.610  -1.636  -3.542  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.284  -1.046  -4.757  0.00  0.00           C+0
HETATM   14  O   UNK     0      -6.129  -1.103  -5.825  0.00  0.00           O+0
HETATM   15  C   UNK     0      -4.081  -0.372  -4.919  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.186  -0.285  -3.850  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.249  -1.108  -1.645  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.267  -1.085  -0.685  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.621  -0.722   0.590  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.378  -0.690   1.572  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.656  -1.069   1.228  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.450   0.083   0.949  0.00  0.00           C+0
HETATM   23  H   UNK     0       0.439   0.818   5.351  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.732  -0.323   5.737  0.00  0.00           H+0
HETATM   25  H   UNK     0       0.093  -0.948   5.523  0.00  0.00           H+0
HETATM   26  H   UNK     0      -1.533   0.267   4.237  0.00  0.00           H+0
HETATM   27  H   UNK     0      -3.263   0.241   2.510  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.982  -2.010  -1.524  0.00  0.00           H+0
HETATM   29  H   UNK     0      -6.550  -2.159  -3.402  0.00  0.00           H+0
HETATM   30  H   UNK     0      -6.936  -1.572  -5.555  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.842   0.092  -5.872  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.256   0.261  -3.993  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.817  -1.430  -2.585  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.437  -0.262   0.625  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.017   0.677   0.136  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.586   0.704   1.840  0.00  0.00           H+0
CONECT    1    2   23   24   25                                             
CONECT    2    3    1                                                       
CONECT    3    4   20    2                                                  
CONECT    4    5    3   26                                                  
CONECT    5    4    6   27                                                  
CONECT    6   19    5    7                                                  
CONECT    7    8    6    9                                                  
CONECT    8    7                                                            
CONECT    9   10    7   17                                                  
CONECT   10    9   11   16                                                  
CONECT   11   10   12   28                                                  
CONECT   12   11   13   29                                                  
CONECT   13   12   15   14                                                  
CONECT   14   13   30                                                       
CONECT   15   13   16   31                                                  
CONECT   16   15   10   32                                                  
CONECT   17    9   18   33                                                  
CONECT   18   19   17                                                       
CONECT   19    6   20   18                                                  
CONECT   20    3   19   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   34   35   36                                             
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    4                                                            
CONECT   27    5                                                            
CONECT   28   11                                                            
CONECT   29   12                                                            
CONECT   30   14                                                            
CONECT   31   15                                                            
CONECT   32   16                                                            
CONECT   33   17                                                            
CONECT   34   22                                                            
CONECT   35   22                                                            
CONECT   36   22                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   76    0
END

RDKit          3D

36 38  0  0  0  0  0  0  0  0999 V2000
    0.8064   -0.1969    5.1678 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132   -0.3869    3.7930 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0711   -0.3564    2.9038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2450   -0.0135    3.2285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2405   -0.0251    2.2456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9250   -0.3836    0.9308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9717   -0.4085   -0.1073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1289   -0.1164    0.1723 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5443   -0.7978   -1.4809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4875   -0.8791   -2.6128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7119   -1.5505   -2.4735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6098   -1.6358   -3.5421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2838   -1.0457   -4.7574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1288   -1.1032   -5.8253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0807   -0.3717   -4.9190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1856   -0.2854   -3.8496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2486   -1.1076   -1.6447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2668   -1.0853   -0.6850 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6205   -0.7218    0.5901 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3779   -0.6904    1.5719 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6555   -1.0694    1.2283 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4500    0.0829    0.9488 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4388    0.8179    5.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7324   -0.3225    5.7372 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0926   -0.9475    5.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5327    0.2666    4.2370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2625    0.2413    2.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9822   -2.0103   -1.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5502   -2.1592   -3.4019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9356   -1.5719   -5.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8416    0.0915   -5.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2565    0.2614   -3.9926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8171   -1.4301   -2.5853 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4366   -0.2623    0.6254 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0168    0.6765    0.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5857    0.7037    1.8404 H   0  0  0  0  0  0  0  0  0  0  0  0
 19  6  1  0
  7  8  2  0
  5  4  1  0
  9 10  1  0
  6  5  2  0
 10 11  2  0
  4  3  2  0
 11 12  1  0
 12 13  2  0
  3 20  1  0
 13 15  1  0
 20 19  2  0
 15 16  2  0
 16 10  1  0
 19 18  1  0
  3  2  1  0
  6  7  1  0
 13 14  1  0
  7  9  1  0
  2  1  1  0
  9 17  2  0
 20 21  1  0
 17 18  1  0
 21 22  1  0
  5 27  1  0
  4 26  1  0
 17 33  1  0
 11 28  1  0
 12 29  1  0
 15 31  1  0
 16 32  1  0
 14 30  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 22 34  1  0
 22 35  1  0
 22 36  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₄O₅

Average Mass

298.2940 Da

Monoisotopic Mass

298.08412 Da

IUPAC Name

3-(4-hydroxyphenyl)-7,8-dimethoxy-4H-chromen-4-one

Traditional Name

3-(4-hydroxyphenyl)-7,8-dimethoxychromen-4-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C([H])=C(C([H])=C1[H])C1=C([H])OC2=C(OC([H])([H])[H])C(OC([H])([H])[H])=C([H])C([H])=C2C1=O

InChI Identifier

InChI=1S/C17H14O5/c1-20-14-8-7-12-15(19)13(9-22-16(12)17(14)21-2)10-3-5-11(18)6-4-10/h3-9,18H,1-2H3

InChI Key

KIVAMNZIYINHSO-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Nocardia species	JEOL database	Maatooq, G. T., et al, Phytochemistry 66, 1007 (2005)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 7-o-methylisoflavones. These are isoflavones with methoxy groups attached to the C7 atom of the isoflavone backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

O-methylated isoflavonoids

Direct Parent

7-O-methylisoflavones

Alternative Parents

Substituents

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

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

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	3.45	ALOGPS
logP	2.72	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	8.96	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	80.65 m³·mol⁻¹	ChemAxon
Polarizability	31.22 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

Not Available

Chemspider ID

14712211

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21270158

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Maatooq, G. T., et al. (2005). Maatooq, G. T., et al, Phytochemistry 66, 1007 (2005) . Phytochem..

Showing NP-Card for 7-O-methyl-8-methoxydaidzein (NP0031192)

MOL for NP0031192 (7-O-methyl-8-methoxydaidzein)

3D MOL for NP0031192 (7-O-methyl-8-methoxydaidzein)

3D SDF for NP0031192 (7-O-methyl-8-methoxydaidzein)

3D-SDF for NP0031192 (7-O-methyl-8-methoxydaidzein)

PDB for NP0031192 (7-O-methyl-8-methoxydaidzein)

3D PDB for NP0031192 (7-O-methyl-8-methoxydaidzein)

SMILES for NP0031192 (7-O-methyl-8-methoxydaidzein)

INCHI for NP0031192 (7-O-methyl-8-methoxydaidzein)

Structure for NP0031192 (7-O-methyl-8-methoxydaidzein)

3D Structure for NP0031192 (7-O-methyl-8-methoxydaidzein)