NP-MRD: Showing NP-Card for 2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one (NP0059721)

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Record Information

Version

2.0

Created at

2022-04-28 04:55:41 UTC

Updated at

2022-04-28 04:55:41 UTC

NP-MRD ID

NP0059721

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one

Description

5-Hydroxy-7,2',5'-trimethoxyflavone 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. Thus, 5-hydroxy-7,2',5'-trimethoxyflavone is considered to be a flavonoid lipid molecule. 2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one is found in Andrographis neesiana. 5-Hydroxy-7,2',5'-trimethoxyflavone is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
   -5.1001    0.7386   -3.0689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7047    0.6569   -2.7389 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3725    0.3647   -1.4265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3321    0.1568   -0.4597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9720   -0.1312    0.8337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6335   -0.2299    1.2437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3482   -0.5240    2.5667 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3650   -0.7272    3.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6784   -0.0252    0.2915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2553   -0.0978    0.5850 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2617   -0.3680    1.8076 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6470   -0.4148    1.9837 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0987   -0.6684    3.1325 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4894   -0.1908    0.9352 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8673   -0.2253    1.0554 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4831   -0.4828    2.2173 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6630    0.0197   -0.0879 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0903    0.2884   -1.3021 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8292    0.5346   -2.4492 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2429    0.5291   -2.4627 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7215    0.3128   -1.3764 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8947    0.0811   -0.2931 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5979    0.1150   -0.4124 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0663    0.2697   -1.0320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6002    1.4759   -2.3761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5697   -0.2405   -2.8646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2213    1.1089   -4.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3693    0.2330   -0.7769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7155   -0.2927    1.5847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1099   -1.4810    3.1273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0047   -1.0588    4.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9418    0.2246    3.5773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3082   -0.5546    2.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2110   -0.6775    3.1160 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7344   -0.0072    0.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6494    1.1437   -3.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5601   -0.5311   -2.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6662    0.9643   -1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2659    0.5248   -2.3343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3052    0.4313   -1.7840 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  2  0
  6  7  1  0
  7  8  1  0
  6  9  1  0
  9 24  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 18 21  1  0
 21 22  2  0
 22 23  1  0
 24  3  1  0
 23 10  1  0
 22 14  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  5 29  1  0
  8 30  1  0
  8 31  1  0
  8 32  1  0
 24 40  1  0
 11 33  1  0
 16 34  1  0
 17 35  1  0
 20 36  1  0
 20 37  1  0
 20 38  1  0
 21 39  1  0
M  END


  Mrv1533004191518552D          

 24 26  0  0  0  0            999 V2000
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  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
   -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 O   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
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    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
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
  3 10  1  0  0  0  0
  9 11  1  0  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
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  2  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 11 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0059721

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(OC)C(=C1)C1=CC(=O)C2=C(O)C=C(OC)C=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C18H16O6/c1-21-10-4-5-15(23-3)12(6-10)16-9-14(20)18-13(19)7-11(22-2)8-17(18)24-16/h4-9,19H,1-3H3

> <INCHI_KEY>
NDJRQOXSFHAYMY-UHFFFAOYSA-N

> <FORMULA>
C18H16O6

> <MOLECULAR_WEIGHT>
328.32

> <EXACT_MASS>
328.094688235

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
33.564410229629466

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(2,5-dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-chromen-4-one

> <ALOGPS_LOGP>
3.26

> <JCHEM_LOGP>
2.84080598

> <ALOGPS_LOGS>
-4.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.518700020220887

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.3648677008984205

> <JCHEM_PKA_STRONGEST_BASIC>
-4.324970457218038

> <JCHEM_POLAR_SURFACE_AREA>
74.22000000000001

> <JCHEM_REFRACTIVITY>
88.34170000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.26e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(2,5-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.334  -6.930   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   11                                                  
CONECT   10    9    3                                                       
CONECT   11    9   12   24                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   23                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23                                                       
CONECT   23   22   15   24                                                  
CONECT   24   23   11                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₆O₆

Average Mass

328.3200 Da

Monoisotopic Mass

328.09469 Da

IUPAC Name

2-(2,5-dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-chromen-4-one

Traditional Name

2-(2,5-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one

CAS Registry Number

Not Available

SMILES

COC1=CC=C(OC)C(=C1)C1=CC(=O)C2=C(O)C=C(OC)C=C2O1

InChI Identifier

InChI=1S/C18H16O6/c1-21-10-4-5-15(23-3)12(6-10)16-9-14(20)18-13(19)7-11(22-2)8-17(18)24-16/h4-9,19H,1-3H3

InChI Key

NDJRQOXSFHAYMY-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
Andrographis neesiana	Plant	KNApSAcK

Chemical Taxonomy

Description

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
3p-methoxyflavonoid-skeleton
7-methoxyflavonoid-skeleton
5-hydroxyflavonoid
Flavone
Hydroxyflavonoid
Chromone
Benzopyran
1-benzopyran
P-dimethoxybenzene
Dimethoxybenzene
Phenoxy compound
Anisole
Phenol ether
Methoxybenzene
Pyranone
Phenol
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Pyran
Benzenoid
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous acid
Organoheterocyclic compound
Oxacycle
Ether
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavones and Flavonols (LMPK12110132 )

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	3.26	ALOGPS
logP	2.84	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	7.36	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	74.22 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	88.34 m³·mol⁻¹	ChemAxon
Polarizability	33.56 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10914422

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one (NP0059721)

MOL for NP0059721 (2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one)

3D MOL for NP0059721 (2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one)

3D SDF for NP0059721 (2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one)

3D-SDF for NP0059721 (2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one)

PDB for NP0059721 (2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one)

3D PDB for NP0059721 (2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one)

SMILES for NP0059721 (2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one)

INCHI for NP0059721 (2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one)

Structure for NP0059721 (2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one)

3D Structure for NP0059721 (2-(2,5-Dimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one)