NP-MRD: Showing NP-Card for 4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin (NP0056811)

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Record Information

Version

2.0

Created at

2022-04-28 02:27:45 UTC

Updated at

2022-04-28 02:27:45 UTC

NP-MRD ID

NP0056811

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin

Description

Derrusnin belongs to the class of organic compounds known as isoflav-3-enones. These are flavonoids with a structure based on an isoflav-3-ene skeleton bearing an oxo-group at position C2. Thus, derrusnin is considered to be a flavonoid lipid molecule. 4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin is found in Derris glabrescens and Derris robusta. Derrusnin is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241504072D          

 26 29  0  0  0  0            999 V2000
    6.9246   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3536   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0681   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7825   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4970   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2115   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7825   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0681   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0681   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3536   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3536   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9966   -3.8404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5117   -3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9966   -2.5055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.3479    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  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  2  0  0  0  0
  3 17  1  0  0  0  0
  8 17  1  0  0  0  0
  4 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 21 25  1  0  0  0  0
 25 26  2  0  0  0  0
 18 26  1  0  0  0  0
M  END

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
    6.2218    1.6856   -0.9867 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5367    0.5631   -0.5323 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1634    0.4418   -0.4025 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6244   -0.7498    0.0693 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2665   -0.9381    0.2230 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6967   -2.0926    0.6831 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4679   -3.1978    1.0418 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3940    0.1064   -0.1070 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0373   -0.0879    0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4990   -1.2869    0.5233 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6750   -1.4044    1.9223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8028    0.9451   -0.2806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2361    0.7473   -0.1262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8953    1.2629    0.9492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2485    1.0573    1.0660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9753    0.3334    0.1150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3182   -0.1937   -0.9776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9607    0.0230   -1.0779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2681   -0.8517   -1.7450 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5739   -0.4517   -1.3217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3064   -0.0129   -0.0070 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2310    2.1109   -0.7450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0101    3.0511   -1.0437 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0722    2.2486   -0.8758 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9303    1.2892   -0.5756 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2934    1.4580   -0.7224 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2101    1.7959   -0.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6772    2.6407   -0.8406 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4946    1.5313   -2.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2998   -1.5531    0.3209 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8957   -3.8835    1.7323 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6837   -3.7948    0.1244 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4352   -2.9277    1.5080 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0281   -0.7290    2.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4997   -2.4313    2.2984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7104   -1.0791    2.1696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4039    1.8414    1.7384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8123    1.4532    1.9098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4477   -0.3875   -1.9301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9581    0.3876   -1.8976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2758   -1.3111   -1.3502 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6794    2.3910   -1.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  2  0
  8 25  1  0
 25 24  1  0
 24 22  1  0
 22 23  2  0
 22 12  1  0
 12  9  2  0
  9 10  1  0
 10 11  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 21  1  0
 21 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  2  0
 25 26  2  0
 26  3  1  0
  9  8  1  0
 18 13  1  0
 17 16  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  7 31  1  0
  7 32  1  0
  7 33  1  0
 11 34  1  0
 11 35  1  0
 11 36  1  0
 14 37  1  0
 15 38  1  0
 20 40  1  0
 20 41  1  0
 18 39  1  0
 26 42  1  0
M  END


  Mrv1533004241504072D          

 26 29  0  0  0  0            999 V2000
    6.9246   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3536   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0681   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7825   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4970   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2115   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7825   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0681   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0681   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3536   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3536   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9966   -3.8404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5117   -3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9966   -2.5055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.3479    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  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  2  0  0  0  0
  3 17  1  0  0  0  0
  8 17  1  0  0  0  0
  4 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 21 25  1  0  0  0  0
 25 26  2  0  0  0  0
 18 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0056811

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(OC)=C2C(OC(=O)C(=C2OC)C2=CC=C3OCOC3=C2)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H16O7/c1-21-11-7-14(22-2)17-15(8-11)26-19(20)16(18(17)23-3)10-4-5-12-13(6-10)25-9-24-12/h4-8H,9H2,1-3H3

> <INCHI_KEY>
PZYZNVLXKYMURF-UHFFFAOYSA-N

> <FORMULA>
C19H16O7

> <MOLECULAR_WEIGHT>
356.33

> <EXACT_MASS>
356.089602855

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
35.73156388990068

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(2H-1,3-benzodioxol-5-yl)-4,5,7-trimethoxy-2H-chromen-2-one

> <ALOGPS_LOGP>
2.65

> <JCHEM_LOGP>
2.118618837333334

> <ALOGPS_LOGS>
-4.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.235025250381112

> <JCHEM_POLAR_SURFACE_AREA>
72.45000000000002

> <JCHEM_REFRACTIVITY>
91.33750000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.21e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
derrusnin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      12.926  -7.463   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      14.260  -6.693   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      14.260  -5.153   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.926  -4.383   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.926  -2.843   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      11.592  -2.073   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      14.260  -2.073   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      15.593  -2.843   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      16.927  -2.073   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      18.261  -2.843   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      19.594  -2.073   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      20.928  -2.843   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      18.261  -4.383   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.927  -5.153   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      16.927  -6.693   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      15.593  -7.463   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      15.593  -4.383   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.592  -5.153   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.592  -6.693   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.259  -7.463   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.925  -6.693   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.460  -7.169   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.555  -5.923   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       7.460  -4.677   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.925  -5.153   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.259  -4.383   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5   18                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   17                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14    3    8                                                  
CONECT   18    4   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   21   26                                                  
CONECT   26   25   18                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₆O₇

Average Mass

356.3300 Da

Monoisotopic Mass

356.08960 Da

IUPAC Name

3-(2H-1,3-benzodioxol-5-yl)-4,5,7-trimethoxy-2H-chromen-2-one

Traditional Name

derrusnin

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C2C(OC(=O)C(=C2OC)C2=CC=C3OCOC3=C2)=C1

InChI Identifier

InChI=1S/C19H16O7/c1-21-11-7-14(22-2)17-15(8-11)26-19(20)16(18(17)23-3)10-4-5-12-13(6-10)25-9-24-12/h4-8H,9H2,1-3H3

InChI Key

PZYZNVLXKYMURF-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
Derris glabrescens	Plant	KNApSAcK
Derris robusta	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoflav-3-enones. These are flavonoids with a structure based on an isoflav-3-ene skeleton bearing an oxo-group at position C2.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Isoflav-3-enes

Direct Parent

Isoflav-3-enones

Alternative Parents

Substituents

Isoflav-3-enone skeleton
Coumarin
Benzopyran
1-benzopyran
Benzodioxole
Anisole
Alkyl aryl ether
Pyranone
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous ester
Lactone
Organoheterocyclic compound
Acetal
Oxacycle
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Other Flavonoids (LMPK12160032 )

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	2.65	ALOGPS
logP	2.12	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	72.45 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	91.34 m³·mol⁻¹	ChemAxon
Polarizability	35.73 Å³	ChemAxon
Number of Rings	4	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

1715307

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin (NP0056811)

MOL for NP0056811 (4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin)

3D MOL for NP0056811 (4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin)

3D SDF for NP0056811 (4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin)

3D-SDF for NP0056811 (4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin)

PDB for NP0056811 (4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin)

3D PDB for NP0056811 (4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin)

SMILES for NP0056811 (4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin)

INCHI for NP0056811 (4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin)

Structure for NP0056811 (4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin)

3D Structure for NP0056811 (4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin)