NP-MRD: Showing NP-Card for 3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone (NP0053301)

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Record Information

Version

2.0

Created at

2022-04-28 00:00:12 UTC

Updated at

2022-04-28 00:00:12 UTC

NP-MRD ID

NP0053301

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone

Description

3,5,8-Trimethoxy-6,7:3',4'-Bis(methylenedioxy)flavone belongs to the class of organic compounds known as 8-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone. Thus, 3,5,8-trimethoxy-6,7:3',4'-Bis(methylenedioxy)flavone is considered to be a flavonoid lipid molecule. 3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone is found in Comptonella microcarpa, Melicope indica, Melicope subunifoliolata and Melicope triphylla. 3,5,8-Trimethoxy-6,7:3',4'-Bis(methylenedioxy)flavone is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 04121520482D          

 29 33  0  0  0  0            999 V2000
    4.9279   -5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -4.8229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0995   -0.3035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9199   -0.2172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2555   -0.9709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6424   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6424   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3569   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3569   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6424   -3.9979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5710   -5.0779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0860   -4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5710   -3.7430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  2  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  2  0  0  0  0
  4 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
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 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  2  0  0  0  0
 21 29  1  0  0  0  0
M  END

     RDKit          3D

 45 49  0  0  0  0  0  0  0  0999 V2000
   -1.5865    0.6150    3.5135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1590    1.3441    2.3558 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3540    0.7375    1.4002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8349    0.0966    0.2905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2382   -0.0207   -0.0314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6278   -0.9144   -1.0302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9280   -1.0690   -1.4363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9173   -0.3247   -0.8534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5477    0.5588    0.1301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2209    0.7200    0.5473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7190    1.1763    0.5476 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8518    0.5535   -0.0211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2961   -0.2442   -1.0304 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0001   -0.4722   -0.5779 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949   -0.4835   -0.4814 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1065   -1.0934   -1.4193 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5570   -1.7266   -2.5162 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3002   -1.0769   -3.7451 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4717   -1.0803   -1.2770 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0533   -0.4455   -0.1746 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2136    0.1523    0.7408 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7528    0.7940    1.8509 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1014    2.1608    1.8432 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8344    0.1562    0.6255 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0386    0.7617    1.5611 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5058    1.3454    2.5699 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4352   -0.5860   -0.2852 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7042   -1.6516   -1.1791 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5475   -1.5868   -2.0204 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8405    0.6875    4.3159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5051    1.1460    3.8664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8892   -0.4128    3.2621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8825   -1.5391   -1.5345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2275   -1.7598   -2.2075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0459    1.4516    1.2984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4537   -0.0133    0.7076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4745    1.3828   -0.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2255   -1.2484   -3.9769 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2034    2.2290    1.6373 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5906    2.7314    1.0446 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9140    2.6648    2.7993 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6797   -2.6369   -0.6677 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6306   -1.4976   -1.7639 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 16  1  0
 16 15  2  0
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 14  4  1  0
  4  3  2  0
  3  2  1  0
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  3 25  1  0
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 20 19  2  0
 19 29  1  0
 29 28  1  0
 28 27  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  2  0
 19 16  1  0
 10  5  1  0
 24 15  1  0
 27 20  1  0
  9  8  1  0
 18 38  1  0
 18 39  1  0
 18 40  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 23 41  1  0
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 23 43  1  0
 28 44  1  0
 28 45  1  0
  6 33  1  0
  7 34  1  0
 12 36  1  0
 12 37  1  0
 10 35  1  0
M  END


  Mrv0541 04121520482D          

 29 33  0  0  0  0            999 V2000
    4.9279   -5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -4.8229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0995   -0.3035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9199   -0.2172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2555   -0.9709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6424   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6424   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3569   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3569   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6424   -3.9979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5710   -5.0779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0860   -4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5710   -3.7430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  2  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  2  0  0  0  0
  4 21  1  0  0  0  0
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 27 28  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  2  0  0  0  0
 21 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0053301

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2OC(=C(OC)C(=O)C2=C(OC)C2=C1OCO2)C1=CC=C2OCOC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H16O9/c1-22-15-12-13(21)17(23-2)14(9-4-5-10-11(6-9)26-7-25-10)29-16(12)18(24-3)20-19(15)27-8-28-20/h4-6H,7-8H2,1-3H3

> <INCHI_KEY>
QIQROODGFFUJKS-UHFFFAOYSA-N

> <FORMULA>
C20H16O9

> <MOLECULAR_WEIGHT>
400.339

> <EXACT_MASS>
400.079432095

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
39.456801232715605

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-(2H-1,3-benzodioxol-5-yl)-4,7,9-trimethoxy-2H,8H-[1,3]dioxolo[4,5-g]chromen-8-one

> <ALOGPS_LOGP>
2.04

> <JCHEM_LOGP>
1.7645125439999996

> <ALOGPS_LOGS>
-3.49

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.173510504242566

> <JCHEM_POLAR_SURFACE_AREA>
90.91000000000003

> <JCHEM_REFRACTIVITY>
98.15

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.30e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(2H-1,3-benzodioxol-5-yl)-4,7,9-trimethoxy-2H-[1,3]dioxolo[4,5-g]chromen-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-APR-15         0                                  
HETATM    1  C   UNK     0       9.199  -9.773   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.865  -9.003   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.865  -7.463   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.531  -6.693   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.531  -5.153   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       7.865  -4.383   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.865  -2.843   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.531  -2.073   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.531  -0.533   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.199  -2.073   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.519  -0.566   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      11.051  -0.406   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.677  -1.812   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      10.533  -2.843   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.533  -4.383   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      11.866  -5.153   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      11.866  -6.693   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.199  -5.153   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.199  -6.693   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      10.533  -7.463   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.198  -7.463   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.198  -9.003   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.864  -9.773   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.530  -9.003   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.066  -9.479   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       0.161  -8.233   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       1.066  -6.987   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.530  -7.463   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.864  -6.693   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5   21                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   18                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   14                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   10   15                                                  
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15    6   19                                                  
CONECT   19   18    3   20                                                  
CONECT   20   19                                                            
CONECT   21    4   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   28                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   24   29                                                  
CONECT   29   28   21                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₆O₉

Average Mass

400.3390 Da

Monoisotopic Mass

400.07943 Da

IUPAC Name

6-(2H-1,3-benzodioxol-5-yl)-4,7,9-trimethoxy-2H,8H-[1,3]dioxolo[4,5-g]chromen-8-one

Traditional Name

6-(2H-1,3-benzodioxol-5-yl)-4,7,9-trimethoxy-2H-[1,3]dioxolo[4,5-g]chromen-8-one

CAS Registry Number

Not Available

SMILES

COC1=C2OC(=C(OC)C(=O)C2=C(OC)C2=C1OCO2)C1=CC=C2OCOC2=C1

InChI Identifier

InChI=1S/C20H16O9/c1-22-15-12-13(21)17(23-2)14(9-4-5-10-11(6-9)26-7-25-10)29-16(12)18(24-3)20-19(15)27-8-28-20/h4-6H,7-8H2,1-3H3

InChI Key

QIQROODGFFUJKS-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Comptonella microcarpa	Plant	KNApSAcK
Melicope indica	Plant	KNApSAcK
Melicope subunifoliolata	LOTUS Database	35616633
Melicope triphylla	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 8-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

8-O-methylated flavonoids

Alternative Parents

Substituents

3-methoxyflavonoid-skeleton
5-methoxyflavonoid-skeleton
8-methoxyflavonoid-skeleton
Flavone
3-methoxychromone
Chromone
Benzopyran
1-benzopyran
Benzodioxole
Anisole
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous ester
Oxacycle
Organoheterocyclic compound
Acetal
Ether
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavones and Flavonols (LMPK12113351 )

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	2.04	ALOGPS
logP	1.76	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	90.91 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	98.15 m³·mol⁻¹	ChemAxon
Polarizability	39.46 Å³	ChemAxon
Number of Rings	5	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

13942548

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone (NP0053301)

MOL for NP0053301 (3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone)

3D MOL for NP0053301 (3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone)

3D SDF for NP0053301 (3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone)

3D-SDF for NP0053301 (3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone)

PDB for NP0053301 (3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone)

3D PDB for NP0053301 (3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone)

SMILES for NP0053301 (3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone)

INCHI for NP0053301 (3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone)

Structure for NP0053301 (3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone)

3D Structure for NP0053301 (3,5,8-Trimethoxy-6,7:3',4'-bis(methylenedioxy)flavone)