NP-MRD: Showing NP-Card for (3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan (NP0062340)

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Record Information

Version

2.0

Created at

2022-04-28 07:01:41 UTC

Updated at

2022-04-28 07:01:41 UTC

NP-MRD ID

NP0062340

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan

Description

COLUTEQUINONE B belongs to the class of organic compounds known as isoflavanquinones. These are isoflavans where the phenyl group carries two C=O groups at position 1 and 4, respectively. (3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan is found in Colutea arborescens. (3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan was first documented in 1998 (PMID: 9548836). Based on a literature review very few articles have been published on COLUTEQUINONE B.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
   -5.8076   -0.8346    1.9405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4654   -1.0941    2.2864 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4235   -0.8260    1.4077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1654   -0.9986    1.8088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0225   -0.7424    0.9565 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1789   -0.8855    1.2758 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2964   -0.2701   -0.4115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1931    0.0207   -1.3618 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6002   -1.2273   -1.5695 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9930   -1.0226   -1.6265 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6254   -0.1644   -0.7316 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8813   -0.4462   -0.2202 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4518    0.4615    0.6725 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7093    0.2356    1.2203 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4954   -0.8807    0.9415 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7502    1.5999    1.0121 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4818    1.8579    0.4785 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9222    0.9681   -0.3967 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6045    1.2219   -0.9618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5453   -0.0949   -0.8208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8195    0.3561   -2.1250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2879    1.7030   -2.2129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6796   -0.3601    0.0574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8759   -0.1825   -0.3637 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4923   -1.1217    2.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9824    0.2153    1.6397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1611   -1.4668    1.0772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9680   -1.3482    2.8218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6674    0.2623   -2.3349 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3243   -1.7475   -2.5232 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4192   -1.9769   -0.7712 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4091   -1.3467   -0.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1123   -0.6952    0.0223 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2094   -1.0956    1.7763 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8995   -1.8068    0.8091 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2125    2.2887    1.7056 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0020    2.7732    0.7979 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7430    1.9384   -1.8216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0390    1.8050   -0.2382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5099    2.3623   -1.7907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3921    1.9030   -3.3137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2312    1.8566   -1.6773 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  1  0
 13 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
  8  7  1  0
  7 20  2  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  2  0
 23  3  1  0
  3  2  1  0
  2  1  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
 12 13  1  0
  5  7  1  0
 11 18  1  0
 15 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 17 37  1  0
 19 38  1  0
 19 39  1  0
  8 29  1  6
  9 30  1  0
  9 31  1  0
 12 32  1  0
 22 40  1  0
 22 41  1  0
 22 42  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
M  END


  Mrv1652304282209012D          

 24 26  0  0  1  0            999 V2000
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
  9 11  1  1  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  2  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
  1 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0062340

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2C[C@@H](COC2=C1)C1=C(OC)C(=O)C(OC)=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H18O6/c1-21-12-5-4-10-6-11(9-24-14(10)7-12)16-13(19)8-15(22-2)17(20)18(16)23-3/h4-5,7-8,11H,6,9H2,1-3H3/t11-/m0/s1

> <INCHI_KEY>
OIIWAPYAJCEIFE-NSHDSACASA-N

> <FORMULA>
C18H18O6

> <MOLECULAR_WEIGHT>
330.336

> <EXACT_MASS>
330.1103383

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
33.7921921693861

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,5-dimethoxy-2-[(3R)-7-methoxy-3,4-dihydro-2H-1-benzopyran-3-yl]cyclohexa-2,5-diene-1,4-dione

> <ALOGPS_LOGP>
1.91

> <JCHEM_LOGP>
1.7624737663333343

> <ALOGPS_LOGS>
-4.03

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.702963000713276

> <JCHEM_PKA_STRONGEST_BASIC>
-4.293154371406838

> <JCHEM_POLAR_SURFACE_AREA>
71.06000000000002

> <JCHEM_REFRACTIVITY>
89.18549999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.06e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,5-dimethoxy-2-[(3R)-7-methoxy-3,4-dihydro-2H-1-benzopyran-3-yl]cyclohexa-2,5-diene-1,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       9.336  -2.310   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
CONECT    1    2    6   23                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9    4                                                       
CONECT   11    9   12   17                                                  
CONECT   12   11   13   21                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   19                                                  
CONECT   16   15   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17                                                            
CONECT   19   15   20                                                       
CONECT   20   19                                                            
CONECT   21   12   22                                                       
CONECT   22   21                                                            
CONECT   23    1   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₈O₆

Average Mass

330.3360 Da

Monoisotopic Mass

330.11034 Da

IUPAC Name

3,5-dimethoxy-2-[(3R)-7-methoxy-3,4-dihydro-2H-1-benzopyran-3-yl]cyclohexa-2,5-diene-1,4-dione

Traditional Name

3,5-dimethoxy-2-[(3R)-7-methoxy-3,4-dihydro-2H-1-benzopyran-3-yl]cyclohexa-2,5-diene-1,4-dione

CAS Registry Number

Not Available

SMILES

COC1=CC=C2C[C@@H](COC2=C1)C1=C(OC)C(=O)C(OC)=CC1=O

InChI Identifier

InChI=1S/C18H18O6/c1-21-12-5-4-10-6-11(9-24-14(10)7-12)16-13(19)8-15(22-2)17(20)18(16)23-3/h4-5,7-8,11H,6,9H2,1-3H3/t11-/m0/s1

InChI Key

OIIWAPYAJCEIFE-NSHDSACASA-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
Colutea arborescens	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoflavanquinones. These are isoflavans where the phenyl group carries two C=O groups at position 1 and 4, respectively.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Isoflavanquinones

Direct Parent

Isoflavanquinones

Alternative Parents

Substituents

Isoflavanquinone
Isoflavanol
Isoflavan
Chromane
1-benzopyran
Benzopyran
Anisole
Quinone
P-benzoquinone
Alkyl aryl ether
Benzenoid
Vinylogous ester
Cyclic ketone
Ketone
Organoheterocyclic compound
Ether
Oxacycle
Organic oxygen compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.91	ALOGPS
logP	1.76	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	2.7	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	71.06 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	89.19 m³·mol⁻¹	ChemAxon
Polarizability	33.79 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

C00018890

Chemspider ID

8195086

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10019513

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Grosvenor PW, Gray DO: Coluteol and Colutequinone B, More Antifungal Isoflavonoids from Colutea arborescens. J Nat Prod. 1998 Jan 23;61(1):99-101. doi: 10.1021/np9703205. [PubMed:9548836 ]

Showing NP-Card for (3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan (NP0062340)

MOL for NP0062340 ((3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan)

3D MOL for NP0062340 ((3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan)

3D SDF for NP0062340 ((3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan)

3D-SDF for NP0062340 ((3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan)

PDB for NP0062340 ((3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan)

3D PDB for NP0062340 ((3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan)

SMILES for NP0062340 ((3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan)

INCHI for NP0062340 ((3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan)

Structure for NP0062340 ((3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan)

3D Structure for NP0062340 ((3R)-2',5'-Diketo-7,4',6'-trimethoxyisoflavan)