NP-MRD: Showing NP-Card for 5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone (NP0042407)

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Record Information

Version

2.0

Created at

2021-06-21 00:04:47 UTC

Updated at

2021-06-30 00:17:28 UTC

NP-MRD ID

NP0042407

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone

Provided By

JEOL Database JEOL Logo

Description

(2S)-5,7-Dihydroxy-2alpha-(2-hydroxy-3-methoxyphenyl)-6,8-dimethyl-2,3-dihydro-4H-1-benzopyran-4-one belongs to the class of organic compounds known as 3'-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C3' atom of the flavonoid backbone. 5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone is found in Pisonia grandis roots. 5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone was first documented in 2013 (Sutthivaiyakit, S., et al.). Based on a literature review very few articles have been published on (2S)-5,7-Dihydroxy-2alpha-(2-hydroxy-3-methoxyphenyl)-6,8-dimethyl-2,3-dihydro-4H-1-benzopyran-4-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212102043D          

 42 44  0  0  0  0            999 V2000
   -4.1447    4.9617    3.2185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1356    4.5236    2.3153 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0554    3.1718    2.0947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8723    2.1966    2.6613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6771    0.8518    2.3358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6655    0.4755    1.4479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8224    1.4372    0.8719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7284    1.0602   -0.1094 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2259    1.1953   -1.5401 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0992    0.8308   -2.4610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0082    1.2931   -3.5957 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8681   -0.1803   -1.9838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9176   -0.6286   -2.8000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1087   -0.1225   -4.0623 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8074   -1.6152   -2.3487 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9423   -2.0838   -3.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5997   -2.1537   -1.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4305   -3.1168   -0.5520 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5387   -1.7324   -0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3642   -2.3112    1.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6948   -0.7119   -0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3085   -0.2939    0.1363 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0436    2.7787    1.2049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2495    3.7438    0.6370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0772    6.0515    3.2908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9830    4.5507    4.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1435    4.7140    2.8442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6689    2.4435    3.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3168    0.0899    2.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5400   -0.5799    1.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1428    1.7055    0.0755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371    2.2233   -1.7543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0630    0.5191   -1.7496 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3995    0.5350   -4.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862   -1.5688   -4.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8987   -1.9046   -2.7168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8363   -3.1534   -3.4289 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1207   -3.3402   -1.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6528   -3.3669    1.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9758   -1.7544    1.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3192   -2.2742    1.4625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5729    4.5877    1.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
  7 23  1  0  0  0  0
 17 15  2  0  0  0  0
 23  3  2  0  0  0  0
 17 19  1  0  0  0  0
  3  4  1  0  0  0  0
 15 13  1  0  0  0  0
  4  5  2  0  0  0  0
 21 22  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
 12 10  1  0  0  0  0
 17 18  1  0  0  0  0
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 13 14  1  0  0  0  0
  8 22  1  0  0  0  0
 10 11  2  0  0  0  0
  9  8  1  0  0  0  0
 23 24  1  0  0  0  0
 13 12  2  0  0  0  0
 19 20  1  0  0  0  0
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  3  2  1  0  0  0  0
  8  7  1  0  0  0  0
  2  1  1  0  0  0  0
  8 31  1  6  0  0  0
  9 32  1  0  0  0  0
  9 33  1  0  0  0  0
  4 28  1  0  0  0  0
  5 29  1  0  0  0  0
  6 30  1  0  0  0  0
 18 38  1  0  0  0  0
 14 34  1  0  0  0  0
 24 42  1  0  0  0  0
 20 39  1  0  0  0  0
 20 40  1  0  0  0  0
 20 41  1  0  0  0  0
 16 35  1  0  0  0  0
 16 36  1  0  0  0  0
 16 37  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
M  END

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
   -4.1447    4.9617    3.2185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1356    4.5236    2.3153 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0554    3.1718    2.0947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8723    2.1966    2.6613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6771    0.8518    2.3358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6655    0.4755    1.4479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8224    1.4372    0.8719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7284    1.0602   -0.1094 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2259    1.1953   -1.5401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0992    0.8308   -2.4610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0082    1.2931   -3.5957 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8681   -0.1803   -1.9838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9176   -0.6286   -2.8000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1087   -0.1225   -4.0623 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8074   -1.6152   -2.3487 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9423   -2.0838   -3.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5997   -2.1537   -1.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4305   -3.1168   -0.5520 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5387   -1.7324   -0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3642   -2.3112    1.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6948   -0.7119   -0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3085   -0.2939    0.1363 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0436    2.7787    1.2049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2495    3.7438    0.6370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0772    6.0515    3.2908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9830    4.5507    4.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1435    4.7140    2.8442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6689    2.4435    3.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3168    0.0899    2.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5400   -0.5799    1.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1428    1.7055    0.0755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371    2.2233   -1.7543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0630    0.5191   -1.7496 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3995    0.5350   -4.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862   -1.5688   -4.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8987   -1.9046   -2.7168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8363   -3.1534   -3.4289 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1207   -3.3402   -1.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6528   -3.3669    1.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9758   -1.7544    1.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3192   -2.2742    1.4625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5729    4.5877    1.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
  7 23  1  0
 17 15  2  0
 23  3  2  0
 17 19  1  0
  3  4  1  0
 15 13  1  0
  4  5  2  0
 21 22  1  0
  5  6  1  0
  6  7  2  0
 12 10  1  0
 17 18  1  0
 10  9  1  0
 13 14  1  0
  8 22  1  0
 10 11  2  0
  9  8  1  0
 23 24  1  0
 13 12  2  0
 19 20  1  0
 21 19  2  0
 15 16  1  0
 21 12  1  0
  3  2  1  0
  8  7  1  0
  2  1  1  0
  8 31  1  6
  9 32  1  0
  9 33  1  0
  4 28  1  0
  5 29  1  0
  6 30  1  0
 18 38  1  0
 14 34  1  0
 24 42  1  0
 20 39  1  0
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 20 41  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
M  END


  Mrv1652306212102043D          

 42 44  0  0  0  0            999 V2000
   -4.1447    4.9617    3.2185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1356    4.5236    2.3153 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0554    3.1718    2.0947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8723    2.1966    2.6613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6771    0.8518    2.3358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6655    0.4755    1.4479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8224    1.4372    0.8719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7284    1.0602   -0.1094 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2259    1.1953   -1.5401 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0992    0.8308   -2.4610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0082    1.2931   -3.5957 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8681   -0.1803   -1.9838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9176   -0.6286   -2.8000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1087   -0.1225   -4.0623 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8074   -1.6152   -2.3487 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9423   -2.0838   -3.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5997   -2.1537   -1.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4305   -3.1168   -0.5520 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5387   -1.7324   -0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3642   -2.3112    1.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6948   -0.7119   -0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3085   -0.2939    0.1363 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0436    2.7787    1.2049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2495    3.7438    0.6370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0772    6.0515    3.2908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9830    4.5507    4.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1435    4.7140    2.8442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6689    2.4435    3.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3168    0.0899    2.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5400   -0.5799    1.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1428    1.7055    0.0755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371    2.2233   -1.7543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0630    0.5191   -1.7496 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3995    0.5350   -4.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862   -1.5688   -4.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8987   -1.9046   -2.7168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8363   -3.1534   -3.4289 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1207   -3.3402   -1.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6528   -3.3669    1.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9758   -1.7544    1.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3192   -2.2742    1.4625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5729    4.5877    1.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
  7 23  1  0  0  0  0
 17 15  2  0  0  0  0
 23  3  2  0  0  0  0
 17 19  1  0  0  0  0
  3  4  1  0  0  0  0
 15 13  1  0  0  0  0
  4  5  2  0  0  0  0
 21 22  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
 12 10  1  0  0  0  0
 17 18  1  0  0  0  0
 10  9  1  0  0  0  0
 13 14  1  0  0  0  0
  8 22  1  0  0  0  0
 10 11  2  0  0  0  0
  9  8  1  0  0  0  0
 23 24  1  0  0  0  0
 13 12  2  0  0  0  0
 19 20  1  0  0  0  0
 21 19  2  0  0  0  0
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 21 12  1  0  0  0  0
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  2  1  1  0  0  0  0
  8 31  1  6  0  0  0
  9 32  1  0  0  0  0
  9 33  1  0  0  0  0
  4 28  1  0  0  0  0
  5 29  1  0  0  0  0
  6 30  1  0  0  0  0
 18 38  1  0  0  0  0
 14 34  1  0  0  0  0
 24 42  1  0  0  0  0
 20 39  1  0  0  0  0
 20 40  1  0  0  0  0
 20 41  1  0  0  0  0
 16 35  1  0  0  0  0
 16 36  1  0  0  0  0
 16 37  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0042407

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(OC([H])([H])[H])C([H])=C([H])C([H])=C1[C@@]1([H])OC2=C(C(O[H])=C(C(O[H])=C2C(=O)C1([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H18O6/c1-8-15(20)9(2)18-14(16(8)21)11(19)7-13(24-18)10-5-4-6-12(23-3)17(10)22/h4-6,13,20-22H,7H2,1-3H3/t13-/m0/s1

> <INCHI_KEY>
GIHOSNHMZHEGQM-ZDUSSCGKSA-N

> <FORMULA>
C18H18O6

> <MOLECULAR_WEIGHT>
330.336

> <EXACT_MASS>
330.1103383

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
34.77608099009058

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-5,7-dihydroxy-2-(2-hydroxy-3-methoxyphenyl)-6,8-dimethyl-3,4-dihydro-2H-1-benzopyran-4-one

> <ALOGPS_LOGP>
2.78

> <JCHEM_LOGP>
3.7042795633333334

> <ALOGPS_LOGS>
-3.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.509945581531209

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.57597858640029

> <JCHEM_PKA_STRONGEST_BASIC>
-4.613076161748466

> <JCHEM_POLAR_SURFACE_AREA>
96.22000000000001

> <JCHEM_REFRACTIVITY>
87.83539999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.62e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-5,7-dihydroxy-2-(2-hydroxy-3-methoxyphenyl)-6,8-dimethyl-2,3-dihydro-1-benzopyran-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
   -4.1447    4.9617    3.2185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1356    4.5236    2.3153 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0554    3.1718    2.0947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8723    2.1966    2.6613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6771    0.8518    2.3358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6655    0.4755    1.4479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8224    1.4372    0.8719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7284    1.0602   -0.1094 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2259    1.1953   -1.5401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0992    0.8308   -2.4610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0082    1.2931   -3.5957 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8681   -0.1803   -1.9838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9176   -0.6286   -2.8000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1087   -0.1225   -4.0623 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8074   -1.6152   -2.3487 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9423   -2.0838   -3.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5997   -2.1537   -1.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4305   -3.1168   -0.5520 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5387   -1.7324   -0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3642   -2.3112    1.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6948   -0.7119   -0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3085   -0.2939    0.1363 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0436    2.7787    1.2049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2495    3.7438    0.6370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0772    6.0515    3.2908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9830    4.5507    4.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1435    4.7140    2.8442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6689    2.4435    3.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3168    0.0899    2.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5400   -0.5799    1.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1428    1.7055    0.0755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371    2.2233   -1.7543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0630    0.5191   -1.7496 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3995    0.5350   -4.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862   -1.5688   -4.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8987   -1.9046   -2.7168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8363   -3.1534   -3.4289 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1207   -3.3402   -1.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6528   -3.3669    1.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9758   -1.7544    1.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3192   -2.2742    1.4625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5729    4.5877    1.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
  7 23  1  0
 17 15  2  0
 23  3  2  0
 17 19  1  0
  3  4  1  0
 15 13  1  0
  4  5  2  0
 21 22  1  0
  5  6  1  0
  6  7  2  0
 12 10  1  0
 17 18  1  0
 10  9  1  0
 13 14  1  0
  8 22  1  0
 10 11  2  0
  9  8  1  0
 23 24  1  0
 13 12  2  0
 19 20  1  0
 21 19  2  0
 15 16  1  0
 21 12  1  0
  3  2  1  0
  8  7  1  0
  2  1  1  0
  8 31  1  6
  9 32  1  0
  9 33  1  0
  4 28  1  0
  5 29  1  0
  6 30  1  0
 18 38  1  0
 14 34  1  0
 24 42  1  0
 20 39  1  0
 20 40  1  0
 20 41  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -4.145   4.962   3.219  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.136   4.524   2.315  0.00  0.00           O+0
HETATM    3  C   UNK     0      -3.055   3.172   2.095  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.872   2.197   2.661  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.677   0.852   2.336  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.666   0.476   1.448  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.822   1.437   0.872  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.728   1.060  -0.109  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.226   1.195  -1.540  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.099   0.831  -2.461  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.008   1.293  -3.596  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.868  -0.180  -1.984  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.918  -0.629  -2.800  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.109  -0.123  -4.062  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.807  -1.615  -2.349  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.942  -2.084  -3.219  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.600  -2.154  -1.065  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.430  -3.117  -0.552  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.539  -1.732  -0.242  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.364  -2.311   1.138  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.695  -0.712  -0.703  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.309  -0.294   0.136  0.00  0.00           O+0
HETATM   23  C   UNK     0      -2.044   2.779   1.205  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.250   3.744   0.637  0.00  0.00           O+0
HETATM   25  H   UNK     0      -4.077   6.051   3.291  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.983   4.551   4.221  0.00  0.00           H+0
HETATM   27  H   UNK     0      -5.144   4.714   2.844  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.669   2.443   3.355  0.00  0.00           H+0
HETATM   29  H   UNK     0      -4.317   0.090   2.776  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.540  -0.580   1.212  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.143   1.706   0.076  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.537   2.223  -1.754  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.063   0.519  -1.750  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.399   0.535  -4.247  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.986  -1.569  -4.183  0.00  0.00           H+0
HETATM   36  H   UNK     0       4.899  -1.905  -2.717  0.00  0.00           H+0
HETATM   37  H   UNK     0       3.836  -3.153  -3.429  0.00  0.00           H+0
HETATM   38  H   UNK     0       4.121  -3.340  -1.195  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.653  -3.367   1.168  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.976  -1.754   1.855  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.319  -2.274   1.462  0.00  0.00           H+0
HETATM   42  H   UNK     0      -1.573   4.588   1.012  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    3    1                                                       
CONECT    3   23    4    2                                                  
CONECT    4    3    5   28                                                  
CONECT    5    4    6   29                                                  
CONECT    6    5    7   30                                                  
CONECT    7   23    6    8                                                  
CONECT    8   22    9    7   31                                             
CONECT    9   10    8   32   33                                             
CONECT   10   12    9   11                                                  
CONECT   11   10                                                            
CONECT   12   10   13   21                                                  
CONECT   13   15   14   12                                                  
CONECT   14   13   34                                                       
CONECT   15   17   13   16                                                  
CONECT   16   15   35   36   37                                             
CONECT   17   15   19   18                                                  
CONECT   18   17   38                                                       
CONECT   19   17   20   21                                                  
CONECT   20   19   39   40   41                                             
CONECT   21   22   19   12                                                  
CONECT   22   21    8                                                       
CONECT   23    7    3   24                                                  
CONECT   24   23   42                                                       
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    4                                                            
CONECT   29    5                                                            
CONECT   30    6                                                            
CONECT   31    8                                                            
CONECT   32    9                                                            
CONECT   33    9                                                            
CONECT   34   14                                                            
CONECT   35   16                                                            
CONECT   36   16                                                            
CONECT   37   16                                                            
CONECT   38   18                                                            
CONECT   39   20                                                            
CONECT   40   20                                                            
CONECT   41   20                                                            
CONECT   42   24                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   88    0
END

RDKit          3D

42 44  0  0  0  0  0  0  0  0999 V2000
   -4.1447    4.9617    3.2185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1356    4.5236    2.3153 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0554    3.1718    2.0947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8723    2.1966    2.6613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6771    0.8518    2.3358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6655    0.4755    1.4479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8224    1.4372    0.8719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7284    1.0602   -0.1094 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2259    1.1953   -1.5401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0992    0.8308   -2.4610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0082    1.2931   -3.5957 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8681   -0.1803   -1.9838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9176   -0.6286   -2.8000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1087   -0.1225   -4.0623 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8074   -1.6152   -2.3487 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9423   -2.0838   -3.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5997   -2.1537   -1.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4305   -3.1168   -0.5520 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5387   -1.7324   -0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3642   -2.3112    1.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6948   -0.7119   -0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3085   -0.2939    0.1363 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0436    2.7787    1.2049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2495    3.7438    0.6370 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0772    6.0515    3.2908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9830    4.5507    4.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1435    4.7140    2.8442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6689    2.4435    3.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3168    0.0899    2.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5400   -0.5799    1.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1428    1.7055    0.0755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371    2.2233   -1.7543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0630    0.5191   -1.7496 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3995    0.5350   -4.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862   -1.5688   -4.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8987   -1.9046   -2.7168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8363   -3.1534   -3.4289 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1207   -3.3402   -1.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6528   -3.3669    1.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9758   -1.7544    1.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3192   -2.2742    1.4625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5729    4.5877    1.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
  7 23  1  0
 17 15  2  0
 23  3  2  0
 17 19  1  0
  3  4  1  0
 15 13  1  0
  4  5  2  0
 21 22  1  0
  5  6  1  0
  6  7  2  0
 12 10  1  0
 17 18  1  0
 10  9  1  0
 13 14  1  0
  8 22  1  0
 10 11  2  0
  9  8  1  0
 23 24  1  0
 13 12  2  0
 19 20  1  0
 21 19  2  0
 15 16  1  0
 21 12  1  0
  3  2  1  0
  8  7  1  0
  2  1  1  0
  8 31  1  6
  9 32  1  0
  9 33  1  0
  4 28  1  0
  5 29  1  0
  6 30  1  0
 18 38  1  0
 14 34  1  0
 24 42  1  0
 20 39  1  0
 20 40  1  0
 20 41  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Value	Source
(2S)-5,7-Dihydroxy-2a-(2-hydroxy-3-methoxyphenyl)-6,8-dimethyl-2,3-dihydro-4H-1-benzopyran-4-one	Generator
(2S)-5,7-Dihydroxy-2α-(2-hydroxy-3-methoxyphenyl)-6,8-dimethyl-2,3-dihydro-4H-1-benzopyran-4-one	Generator

Chemical Formula

C₁₈H₁₈O₆

Average Mass

330.3360 Da

Monoisotopic Mass

330.11034 Da

IUPAC Name

(2S)-5,7-dihydroxy-2-(2-hydroxy-3-methoxyphenyl)-6,8-dimethyl-3,4-dihydro-2H-1-benzopyran-4-one

Traditional Name

(2S)-5,7-dihydroxy-2-(2-hydroxy-3-methoxyphenyl)-6,8-dimethyl-2,3-dihydro-1-benzopyran-4-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C(OC([H])([H])[H])C([H])=C([H])C([H])=C1[C@@]1([H])OC2=C(C(O[H])=C(C(O[H])=C2C(=O)C1([H])[H])C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C18H18O6/c1-8-15(20)9(2)18-14(16(8)21)11(19)7-13(24-18)10-5-4-6-12(23-3)17(10)22/h4-6,13,20-22H,7H2,1-3H3/t13-/m0/s1

InChI Key

GIHOSNHMZHEGQM-ZDUSSCGKSA-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
Pisonia grandis roots	JEOL database	Sutthivaiyakit, S., et al, Phytochem. Lett. 6, 407 (2013)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3'-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C3' atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

3'-O-methylated flavonoids

Alternative Parents

Substituents

3p-methoxyflavonoid-skeleton
Hydroxyflavonoid
5-hydroxyflavonoid
7-hydroxyflavonoid
Flavanone
Flavan
Chromone
Methoxyphenol
Chromane
Benzopyran
1-benzopyran
Phenoxy compound
Methoxybenzene
Anisole
Aryl ketone
Aryl alkyl ketone
Phenol ether
Phenol
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Vinylogous acid
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Organic oxide
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
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	2.78	ALOGPS
logP	3.7	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	8.58	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	87.84 m³·mol⁻¹	ChemAxon
Polarizability	34.78 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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102442860

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Sutthivaiyakit, S., et al. (2013). Sutthivaiyakit, S., et al, Phytochem. Lett. 6, 407 (2013). Phytochem..

Showing NP-Card for 5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone (NP0042407)

MOL for NP0042407 (5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone)

3D MOL for NP0042407 (5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone)

3D SDF for NP0042407 (5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone)

3D-SDF for NP0042407 (5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone)

PDB for NP0042407 (5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone)

3D PDB for NP0042407 (5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone)

SMILES for NP0042407 (5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone)

INCHI for NP0042407 (5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone)

Structure for NP0042407 (5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone)

3D Structure for NP0042407 (5,7,2'-trihydroxy-30-methoxy-6,8-dimethylflavanone)