NP-MRD: Showing NP-Card for 5,7,2'-trimethoxyflavone (NP0028320)

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Record Information

Version

2.0

Created at

2021-06-19 20:14:35 UTC

Updated at

2021-06-29 23:55:01 UTC

NP-MRD ID

NP0028320

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,7,2'-trimethoxyflavone

Provided By

JEOL Database JEOL Logo

Description

5,7,2'-trimethoxyflavone is found in Andrographis viscosula. 5,7,2'-trimethoxyflavone was first documented in 2002 (Rao, Y. K., et al.). Based on a literature review very few articles have been published on 5,7-dimethoxy-2-(2-methoxyphenyl)-4H-chromen-4-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192122143D          

 39 41  0  0  0  0            999 V2000
   -0.6935    4.4105    0.9413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6264    2.9976    0.7881 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0282    2.5253   -0.3467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5400    3.2983   -1.3577 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1339    2.6816   -2.4684 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258    3.5115   -3.4415 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0111    3.7793   -3.2179 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1312    1.2872   -2.5965 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7079    0.5759   -3.7582 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2609    1.1325   -4.6975 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6065   -0.8929   -3.7469 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0398   -1.5076   -2.7011 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9073   -2.9775   -2.6472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3781   -3.5160   -2.4604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5738   -4.8951   -2.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5140   -5.7525   -2.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8000   -5.2351   -2.7040 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0105   -3.8513   -2.7615 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2429   -3.2658   -2.9114 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3743   -4.1205   -3.0096 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4987   -0.8511   -1.6114 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5558    0.5206   -1.5829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0132    1.1346   -0.4636 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3083    4.8489    0.9974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2023    4.6202    1.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2814    4.8670    0.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5351    4.3826   -1.3197 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3938    4.3170   -4.0904 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5965    2.8610   -3.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1395    4.4209   -2.3394 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0150   -1.4186   -4.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2390   -2.8570   -2.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5737   -5.2974   -2.2618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3640   -6.8285   -2.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6181   -5.9426   -2.7896 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5003   -4.7154   -2.0992 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2611   -3.4887   -3.1187 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3105   -4.7591   -3.8967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4570    0.5240    0.3196 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0  0  0  0
 13 18  2  0  0  0  0
  8 22  2  0  0  0  0
 18 17  1  0  0  0  0
  8  9  1  0  0  0  0
 17 16  2  0  0  0  0
 22 23  1  0  0  0  0
 16 15  1  0  0  0  0
  9 11  1  0  0  0  0
 15 14  2  0  0  0  0
 14 13  1  0  0  0  0
 12 13  1  0  0  0  0
 23  3  2  0  0  0  0
  9 10  2  0  0  0  0
 11 12  2  0  0  0  0
  3  2  1  0  0  0  0
  3  4  1  0  0  0  0
  2  1  1  0  0  0  0
 12 21  1  0  0  0  0
  5  6  1  0  0  0  0
  4  5  2  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 31  1  0  0  0  0
 23 39  1  0  0  0  0
  4 27  1  0  0  0  0
 17 35  1  0  0  0  0
 16 34  1  0  0  0  0
 15 33  1  0  0  0  0
 14 32  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
  7 28  1  0  0  0  0
  7 29  1  0  0  0  0
  7 30  1  0  0  0  0
 20 36  1  0  0  0  0
 20 37  1  0  0  0  0
 20 38  1  0  0  0  0
M  END

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
   -0.6935    4.4105    0.9413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6264    2.9976    0.7881 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0282    2.5253   -0.3467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5400    3.2983   -1.3577 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1339    2.6816   -2.4684 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258    3.5115   -3.4415 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0111    3.7793   -3.2179 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1312    1.2872   -2.5965 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7079    0.5759   -3.7582 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2609    1.1325   -4.6975 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6065   -0.8929   -3.7469 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0398   -1.5076   -2.7011 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9073   -2.9775   -2.6472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3781   -3.5160   -2.4604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5738   -4.8951   -2.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5140   -5.7525   -2.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8000   -5.2351   -2.7040 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0105   -3.8513   -2.7615 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2429   -3.2658   -2.9114 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3743   -4.1205   -3.0096 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4987   -0.8511   -1.6114 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5558    0.5206   -1.5829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0132    1.1346   -0.4636 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3083    4.8489    0.9974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2023    4.6202    1.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2814    4.8670    0.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5351    4.3826   -1.3197 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3938    4.3170   -4.0904 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5965    2.8610   -3.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1395    4.4209   -2.3394 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0150   -1.4186   -4.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2390   -2.8570   -2.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5737   -5.2974   -2.2618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3640   -6.8285   -2.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6181   -5.9426   -2.7896 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5003   -4.7154   -2.0992 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2611   -3.4887   -3.1187 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3105   -4.7591   -3.8967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4570    0.5240    0.3196 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 13 18  2  0
  8 22  2  0
 18 17  1  0
  8  9  1  0
 17 16  2  0
 22 23  1  0
 16 15  1  0
  9 11  1  0
 15 14  2  0
 14 13  1  0
 12 13  1  0
 23  3  2  0
  9 10  2  0
 11 12  2  0
  3  2  1  0
  3  4  1  0
  2  1  1  0
 12 21  1  0
  5  6  1  0
  4  5  2  0
  6  7  1  0
  5  8  1  0
 18 19  1  0
 19 20  1  0
 11 31  1  0
 23 39  1  0
  4 27  1  0
 17 35  1  0
 16 34  1  0
 15 33  1  0
 14 32  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  7 28  1  0
  7 29  1  0
  7 30  1  0
 20 36  1  0
 20 37  1  0
 20 38  1  0
M  END


  Mrv1652306192122143D          

 39 41  0  0  0  0            999 V2000
   -0.6935    4.4105    0.9413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6264    2.9976    0.7881 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0282    2.5253   -0.3467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5400    3.2983   -1.3577 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1339    2.6816   -2.4684 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258    3.5115   -3.4415 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0111    3.7793   -3.2179 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1312    1.2872   -2.5965 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7079    0.5759   -3.7582 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2609    1.1325   -4.6975 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6065   -0.8929   -3.7469 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0398   -1.5076   -2.7011 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9073   -2.9775   -2.6472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3781   -3.5160   -2.4604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5738   -4.8951   -2.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5140   -5.7525   -2.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8000   -5.2351   -2.7040 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0105   -3.8513   -2.7615 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2429   -3.2658   -2.9114 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3743   -4.1205   -3.0096 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4987   -0.8511   -1.6114 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5558    0.5206   -1.5829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0132    1.1346   -0.4636 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3083    4.8489    0.9974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2023    4.6202    1.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2814    4.8670    0.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5351    4.3826   -1.3197 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3938    4.3170   -4.0904 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5965    2.8610   -3.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1395    4.4209   -2.3394 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0150   -1.4186   -4.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2390   -2.8570   -2.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5737   -5.2974   -2.2618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3640   -6.8285   -2.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6181   -5.9426   -2.7896 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5003   -4.7154   -2.0992 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2611   -3.4887   -3.1187 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3105   -4.7591   -3.8967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4570    0.5240    0.3196 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0  0  0  0
 13 18  2  0  0  0  0
  8 22  2  0  0  0  0
 18 17  1  0  0  0  0
  8  9  1  0  0  0  0
 17 16  2  0  0  0  0
 22 23  1  0  0  0  0
 16 15  1  0  0  0  0
  9 11  1  0  0  0  0
 15 14  2  0  0  0  0
 14 13  1  0  0  0  0
 12 13  1  0  0  0  0
 23  3  2  0  0  0  0
  9 10  2  0  0  0  0
 11 12  2  0  0  0  0
  3  2  1  0  0  0  0
  3  4  1  0  0  0  0
  2  1  1  0  0  0  0
 12 21  1  0  0  0  0
  5  6  1  0  0  0  0
  4  5  2  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 31  1  0  0  0  0
 23 39  1  0  0  0  0
  4 27  1  0  0  0  0
 17 35  1  0  0  0  0
 16 34  1  0  0  0  0
 15 33  1  0  0  0  0
 14 32  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
  7 28  1  0  0  0  0
  7 29  1  0  0  0  0
  7 30  1  0  0  0  0
 20 36  1  0  0  0  0
 20 37  1  0  0  0  0
 20 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0028320

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C1=C([H])C(OC([H])([H])[H])=C(C([H])=C1[H])C1=C([H])C(=O)C2=C(O1)C([H])=C(OC([H])([H])[H])C([H])=C2OC([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H16O5/c1-20-11-8-16(22-3)18-13(19)10-15(23-17(18)9-11)12-6-4-5-7-14(12)21-2/h4-10H,1-3H3

> <INCHI_KEY>
IAVDTHSFRQVKKU-UHFFFAOYSA-N

> <FORMULA>
C18H16O5

> <MOLECULAR_WEIGHT>
312.321

> <EXACT_MASS>
312.099773615

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
33.18559771338953

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,7-dimethoxy-2-(2-methoxyphenyl)-4H-chromen-4-one

> <ALOGPS_LOGP>
3.22

> <JCHEM_LOGP>
2.494371301666667

> <ALOGPS_LOGS>
-4.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.865872641055773

> <JCHEM_PKA_STRONGEST_BASIC>
-4.354118899928742

> <JCHEM_POLAR_SURFACE_AREA>
53.99000000000001

> <JCHEM_REFRACTIVITY>
86.36080000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.11e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,7-dimethoxy-2-(2-methoxyphenyl)chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
   -0.6935    4.4105    0.9413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6264    2.9976    0.7881 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0282    2.5253   -0.3467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5400    3.2983   -1.3577 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1339    2.6816   -2.4684 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258    3.5115   -3.4415 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0111    3.7793   -3.2179 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1312    1.2872   -2.5965 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7079    0.5759   -3.7582 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2609    1.1325   -4.6975 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6065   -0.8929   -3.7469 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0398   -1.5076   -2.7011 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9073   -2.9775   -2.6472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3781   -3.5160   -2.4604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5738   -4.8951   -2.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5140   -5.7525   -2.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8000   -5.2351   -2.7040 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0105   -3.8513   -2.7615 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2429   -3.2658   -2.9114 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3743   -4.1205   -3.0096 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4987   -0.8511   -1.6114 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5558    0.5206   -1.5829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0132    1.1346   -0.4636 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3083    4.8489    0.9974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2023    4.6202    1.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2814    4.8670    0.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5351    4.3826   -1.3197 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3938    4.3170   -4.0904 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5965    2.8610   -3.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1395    4.4209   -2.3394 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0150   -1.4186   -4.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2390   -2.8570   -2.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5737   -5.2974   -2.2618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3640   -6.8285   -2.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6181   -5.9426   -2.7896 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5003   -4.7154   -2.0992 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2611   -3.4887   -3.1187 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3105   -4.7591   -3.8967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4570    0.5240    0.3196 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 13 18  2  0
  8 22  2  0
 18 17  1  0
  8  9  1  0
 17 16  2  0
 22 23  1  0
 16 15  1  0
  9 11  1  0
 15 14  2  0
 14 13  1  0
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 23  3  2  0
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 11 12  2  0
  3  2  1  0
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  5  6  1  0
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  6  7  1  0
  5  8  1  0
 18 19  1  0
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 23 39  1  0
  4 27  1  0
 17 35  1  0
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  1 24  1  0
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  7 28  1  0
  7 29  1  0
  7 30  1  0
 20 36  1  0
 20 37  1  0
 20 38  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.694   4.410   0.941  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.626   2.998   0.788  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.028   2.525  -0.347  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.540   3.298  -1.358  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.134   2.682  -2.468  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.626   3.511  -3.442  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.011   3.779  -3.218  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.131   1.287  -2.596  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.708   0.576  -3.758  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.261   1.133  -4.697  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.607  -0.893  -3.747  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.040  -1.508  -2.701  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.907  -2.978  -2.647  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.378  -3.516  -2.460  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.574  -4.895  -2.403  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.514  -5.753  -2.527  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.800  -5.235  -2.704  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.010  -3.851  -2.761  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.243  -3.266  -2.911  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.374  -4.120  -3.010  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.499  -0.851  -1.611  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.556   0.521  -1.583  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.013   1.135  -0.464  0.00  0.00           C+0
HETATM   24  H   UNK     0       0.308   4.849   0.997  0.00  0.00           H+0
HETATM   25  H   UNK     0      -1.202   4.620   1.887  0.00  0.00           H+0
HETATM   26  H   UNK     0      -1.281   4.867   0.138  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.535   4.383  -1.320  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.394   4.317  -4.090  0.00  0.00           H+0
HETATM   29  H   UNK     0       3.596   2.861  -3.100  0.00  0.00           H+0
HETATM   30  H   UNK     0       3.139   4.421  -2.339  0.00  0.00           H+0
HETATM   31  H   UNK     0       2.015  -1.419  -4.601  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.239  -2.857  -2.364  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.574  -5.297  -2.262  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.364  -6.829  -2.483  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.618  -5.943  -2.790  0.00  0.00           H+0
HETATM   36  H   UNK     0       4.500  -4.715  -2.099  0.00  0.00           H+0
HETATM   37  H   UNK     0       5.261  -3.489  -3.119  0.00  0.00           H+0
HETATM   38  H   UNK     0       4.311  -4.759  -3.897  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.457   0.524   0.320  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    3    1                                                       
CONECT    3   23    2    4                                                  
CONECT    4    3    5   27                                                  
CONECT    5    6    4    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6   28   29   30                                             
CONECT    8   22    9    5                                                  
CONECT    9    8   11   10                                                  
CONECT   10    9                                                            
CONECT   11    9   12   31                                                  
CONECT   12   13   11   21                                                  
CONECT   13   18   14   12                                                  
CONECT   14   15   13   32                                                  
CONECT   15   16   14   33                                                  
CONECT   16   17   15   34                                                  
CONECT   17   18   16   35                                                  
CONECT   18   13   17   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   36   37   38                                             
CONECT   21   22   12                                                       
CONECT   22   21    8   23                                                  
CONECT   23   22    3   39                                                  
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    4                                                            
CONECT   28    7                                                            
CONECT   29    7                                                            
CONECT   30    7                                                            
CONECT   31   11                                                            
CONECT   32   14                                                            
CONECT   33   15                                                            
CONECT   34   16                                                            
CONECT   35   17                                                            
CONECT   36   20                                                            
CONECT   37   20                                                            
CONECT   38   20                                                            
CONECT   39   23                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   82    0
END

RDKit          3D

39 41  0  0  0  0  0  0  0  0999 V2000
   -0.6935    4.4105    0.9413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6264    2.9976    0.7881 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0282    2.5253   -0.3467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5400    3.2983   -1.3577 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1339    2.6816   -2.4684 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258    3.5115   -3.4415 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0111    3.7793   -3.2179 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1312    1.2872   -2.5965 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7079    0.5759   -3.7582 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2609    1.1325   -4.6975 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6065   -0.8929   -3.7469 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0398   -1.5076   -2.7011 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9073   -2.9775   -2.6472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3781   -3.5160   -2.4604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5738   -4.8951   -2.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5140   -5.7525   -2.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8000   -5.2351   -2.7040 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0105   -3.8513   -2.7615 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2429   -3.2658   -2.9114 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3743   -4.1205   -3.0096 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4987   -0.8511   -1.6114 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5558    0.5206   -1.5829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0132    1.1346   -0.4636 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3083    4.8489    0.9974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2023    4.6202    1.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2814    4.8670    0.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5351    4.3826   -1.3197 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3938    4.3170   -4.0904 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5965    2.8610   -3.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1395    4.4209   -2.3394 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0150   -1.4186   -4.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2390   -2.8570   -2.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5737   -5.2974   -2.2618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3640   -6.8285   -2.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6181   -5.9426   -2.7896 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5003   -4.7154   -2.0992 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2611   -3.4887   -3.1187 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3105   -4.7591   -3.8967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4570    0.5240    0.3196 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 13 18  2  0
  8 22  2  0
 18 17  1  0
  8  9  1  0
 17 16  2  0
 22 23  1  0
 16 15  1  0
  9 11  1  0
 15 14  2  0
 14 13  1  0
 12 13  1  0
 23  3  2  0
  9 10  2  0
 11 12  2  0
  3  2  1  0
  3  4  1  0
  2  1  1  0
 12 21  1  0
  5  6  1  0
  4  5  2  0
  6  7  1  0
  5  8  1  0
 18 19  1  0
 19 20  1  0
 11 31  1  0
 23 39  1  0
  4 27  1  0
 17 35  1  0
 16 34  1  0
 15 33  1  0
 14 32  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  7 28  1  0
  7 29  1  0
  7 30  1  0
 20 36  1  0
 20 37  1  0
 20 38  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₆O₅

Average Mass

312.3210 Da

Monoisotopic Mass

312.09977 Da

IUPAC Name

5,7-dimethoxy-2-(2-methoxyphenyl)-4H-chromen-4-one

Traditional Name

5,7-dimethoxy-2-(2-methoxyphenyl)chromen-4-one

CAS Registry Number

Not Available

SMILES

[H]C1=C([H])C(OC([H])([H])[H])=C(C([H])=C1[H])C1=C([H])C(=O)C2=C(O1)C([H])=C(OC([H])([H])[H])C([H])=C2OC([H])([H])[H]

InChI Identifier

InChI=1S/C18H16O5/c1-20-11-8-16(22-3)18-13(19)10-15(23-17(18)9-11)12-6-4-5-7-14(12)21-2/h4-10H,1-3H3

InChI Key

IAVDTHSFRQVKKU-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
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, 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, 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, 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
Andrographis viscosula	JEOL database	Rao, Y. K., et al, Phytochemistry 61, 927 (2002)

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

7-O-methylated flavonoids

Alternative Parents

Substituents

2p-methoxyflavonoid-skeleton
5-methoxyflavonoid-skeleton
7-methoxyflavonoid-skeleton
Flavone
Chromone
Benzopyran
1-benzopyran
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
Pyranone
Benzenoid
Monocyclic benzene moiety
Pyran
Vinylogous ester
Heteroaromatic compound
Ether
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavones and Flavonols (LMPK12110130 )

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	3.22	ALOGPS
logP	2.49	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	14.87	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	53.99 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	86.36 m³·mol⁻¹	ChemAxon
Polarizability	33.19 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

C00013295

Chemspider ID

4479679

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

Rao, Y. K., et al. (2002). Rao, Y. K., et al, Phytochemistry 61, 927 (2002). Phytochem..

Showing NP-Card for 5,7,2'-trimethoxyflavone (NP0028320)

MOL for NP0028320 (5,7,2'-trimethoxyflavone)

3D MOL for NP0028320 (5,7,2'-trimethoxyflavone)

3D SDF for NP0028320 (5,7,2'-trimethoxyflavone)

3D-SDF for NP0028320 (5,7,2'-trimethoxyflavone)

PDB for NP0028320 (5,7,2'-trimethoxyflavone)

3D PDB for NP0028320 (5,7,2'-trimethoxyflavone)

SMILES for NP0028320 (5,7,2'-trimethoxyflavone)

INCHI for NP0028320 (5,7,2'-trimethoxyflavone)

Structure for NP0028320 (5,7,2'-trimethoxyflavone)

3D Structure for NP0028320 (5,7,2'-trimethoxyflavone)