NP-MRD: Showing NP-Card for 4'-O-Methyltectorigenin (NP0051472)

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Record Information

Version

2.0

Created at

2022-04-27 22:49:33 UTC

Updated at

2022-04-27 22:49:33 UTC

NP-MRD ID

NP0051472

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4'-O-Methyltectorigenin

Description

5,7-Dihydroxy-6-methoxy-3-(4-methoxyphenyl)-4H-chromen-4-one belongs to the class of organic compounds known as 4'-o-methylisoflavones. These are isoflavones with methoxy groups attached to the C4' atom of the isoflavone backbone. Thus, 5,7-dihydroxy-6-methoxy-3-(4-methoxyphenyl)-4H-chromen-4-one is considered to be a flavonoid lipid molecule. 4'-O-Methyltectorigenin is found in Araucaria angustifolia, Dalbergia sissoo, Iris germanica , Iris japonica , Iris kashmiriana, Iris nepalensis , Iris pseudacorus, Iris pseudopumila, Iris tingitana, Medicago truncatula, Pericopsis laxiflora , Pericopsis mooniana, Sundacarpus amarus, Pueraria montana, Pueraria montana var. lobata, Pueraria thunbergiana , Sophora tomentosa, Sophora japonica , Virola surinamensis and Wisteria brachybotrys. 5,7-Dihydroxy-6-methoxy-3-(4-methoxyphenyl)-4H-chromen-4-one is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 39  0  0  0  0  0  0  0  0999 V2000
    6.8092    0.5725   -0.8129 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9330   -0.5207   -0.9878 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6144   -0.3959   -0.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1719    0.7732   -0.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8763    0.8976    0.3552 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9790   -0.1394    0.2068 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6170    0.0297    0.6324 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3241    0.6099    1.8485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8874    0.7727    2.2528 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8859    0.3855    1.5078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1975    0.5662    1.9546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2642    0.1635    1.1814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5696    0.3595    1.6596 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0757   -0.4304   -0.0573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1689   -0.8351   -0.8333 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7181    0.0881   -1.7410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7812   -0.6011   -0.4825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5263   -1.1832   -1.7006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7010   -0.2033    0.2798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4086   -0.3915   -0.1814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2230   -0.9296   -1.3046 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3854   -1.3317   -0.3465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7033   -1.4411   -0.7381 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0660    0.7570    0.2443 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3480    1.4790   -1.2898 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7162    0.3596   -1.4190 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8579    1.6170    0.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5744    1.8610    0.7952 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1108    0.9584    2.5255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3281    1.0296    2.9202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3566    0.0663    1.0970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7327   -0.1959   -2.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7622    1.1191   -1.2986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0425    0.1578   -2.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2497   -1.5052   -2.3261 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6919   -2.1764   -0.4773 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1005   -2.3427   -1.1804 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 22  1  0
 22 23  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 19  2  0
 19 17  1  0
 17 18  1  0
 17 14  2  0
 14 15  1  0
 15 16  1  0
 14 12  1  0
 12 13  1  0
 12 11  2  0
 19 20  1  0
 20 21  2  0
 23  3  1  0
 20  7  1  0
 11 10  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  5 28  1  0
 22 36  1  0
 23 37  1  0
  8 29  1  0
 18 35  1  0
 16 32  1  0
 16 33  1  0
 16 34  1  0
 13 31  1  0
 11 30  1  0
M  END

  Mrv1652309171720512D          

 23 25  0  0  0  0            999 V2000
    6.4302    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   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
    1.4289    0.8250    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    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    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
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    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
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   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
  5  3  1  0  0  0  0
  6  4  2  0  0  0  0
  9  3  2  0  0  0  0
  9  4  1  0  0  0  0
 10  5  2  0  0  0  0
 10  6  1  0  0  0  0
 11  8  2  0  0  0  0
 11  9  1  0  0  0  0
 12  7  2  0  0  0  0
 13  7  1  0  0  0  0
 14 13  2  0  0  0  0
 15 11  1  0  0  0  0
 15 14  1  0  0  0  0
 16 14  1  0  0  0  0
 17 12  1  0  0  0  0
 17 16  2  0  0  0  0
 18 12  1  0  0  0  0
 19 15  2  0  0  0  0
 20 16  1  0  0  0  0
 21  1  1  0  0  0  0
 21 10  1  0  0  0  0
 22  2  1  0  0  0  0
 22 17  1  0  0  0  0
 23  8  1  0  0  0  0
 23 13  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0051472

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1)C1=COC2=C(C(O)=C(OC)C(O)=C2)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H14O6/c1-21-10-5-3-9(4-6-10)11-8-23-13-7-12(18)17(22-2)16(20)14(13)15(11)19/h3-8,18,20H,1-2H3

> <INCHI_KEY>
VOOFPOMXNLNEOF-UHFFFAOYSA-N

> <FORMULA>
C17H14O6

> <MOLECULAR_WEIGHT>
314.2895

> <EXACT_MASS>
314.07903818

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
31.703385851522444

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,7-dihydroxy-6-methoxy-3-(4-methoxyphenyl)-4H-chromen-4-one

> <ALOGPS_LOGP>
3.27

> <JCHEM_LOGP>
3.0650951799999993

> <ALOGPS_LOGS>
-3.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.652376279001851

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.07260621937242

> <JCHEM_PKA_STRONGEST_BASIC>
-4.515094266798383

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
82.6284

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.52e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
irisolidone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-SEP-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-SEP-17         0                                  
HETATM    1  C   UNK     0      12.003   8.470   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336   6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669   6.160   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.000   1.540   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       5.335   6.160   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      12.003   6.930   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       0.000   4.620   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
CONECT    1   21                                                            
CONECT    2   22                                                            
CONECT    3    5    9                                                       
CONECT    4    6    9                                                       
CONECT    5    3   10                                                       
CONECT    6    4   10                                                       
CONECT    7   12   13                                                       
CONECT    8   11   23                                                       
CONECT    9    3    4   11                                                  
CONECT   10    5    6   21                                                  
CONECT   11    8    9   15                                                  
CONECT   12    7   17   18                                                  
CONECT   13    7   14   23                                                  
CONECT   14   13   15   16                                                  
CONECT   15   11   14   19                                                  
CONECT   16   14   17   20                                                  
CONECT   17   12   16   22                                                  
CONECT   18   12                                                            
CONECT   19   15                                                            
CONECT   20   16                                                            
CONECT   21    1   10                                                       
CONECT   22    2   17                                                       
CONECT   23    8   13                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₄O₆

Average Mass

314.2895 Da

Monoisotopic Mass

314.07904 Da

IUPAC Name

5,7-dihydroxy-6-methoxy-3-(4-methoxyphenyl)-4H-chromen-4-one

Traditional Name

irisolidone

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)C1=COC2=C(C(O)=C(OC)C(O)=C2)C1=O

InChI Identifier

InChI=1S/C17H14O6/c1-21-10-5-3-9(4-6-10)11-8-23-13-7-12(18)17(22-2)16(20)14(13)15(11)19/h3-8,18,20H,1-2H3

InChI Key

VOOFPOMXNLNEOF-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
Araucaria angustifolia	Plant	KNApSAcK
Dalbergia sissoo	LOTUS Database	35616633
Iris germanica	Plant	KNApSAcK
Iris japonica	Plant	KNApSAcK
Iris kashmiriana	Plant	KNApSAcK
Iris nepalensis	Plant	KNApSAcK
Iris pseudacorus	LOTUS Database	35616633
Iris pseudopumila	LOTUS Database	35616633
Iris tingitana	Plant	KNApSAcK
Medicago truncatula	Plant	KNApSAcK
Pericopsis laxiflora	Plant	KNApSAcK
Pericopsis mooniana	Plant	KNApSAcK
Prumnopitys amara	LOTUS Database	35616633
Pueraria montana	LOTUS Database	35616633
Pueraria montana var. lobata	Plant	KNApSAcK
Pueraria thunbergiana	Plant	KNApSAcK
Sophora tomentosa	LOTUS Database	35616633
Styphnolobium japonicum	Plant	KNApSAcK
Virola surinamensis	LOTUS Database	35616633
Wisteria brachybotrys	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 4'-o-methylisoflavones. These are isoflavones with methoxy groups attached to the C4' atom of the isoflavone backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

O-methylated isoflavonoids

Direct Parent

4'-O-methylisoflavones

Alternative Parents

Substituents

4p-o-methylisoflavone
Isoflavone
Hydroxyisoflavonoid
Chromone
Benzopyran
1-benzopyran
Anisole
Phenoxy compound
Phenol ether
Methoxybenzene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Pyran
Vinylogous acid
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

methoxyisoflavone (CHEBI:5972 )
isoflavones (C10471 )
Isoflavonoids (C10471 )
Isoflavonoids (LMPK12050384 )

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	3.27	ALOGPS
logP	3.07	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	7.07	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	82.63 m³·mol⁻¹	ChemAxon
Polarizability	31.7 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

HMDB0132852

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB029977

KNApSAcK ID

C00002540

Chemspider ID

Not Available

KEGG Compound ID

C10471

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5281781

PDB ID

Not Available

ChEBI ID

5972

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 4'-O-Methyltectorigenin (NP0051472)

MOL for NP0051472 (4'-O-Methyltectorigenin)

3D MOL for NP0051472 (4'-O-Methyltectorigenin)

3D SDF for NP0051472 (4'-O-Methyltectorigenin)

3D-SDF for NP0051472 (4'-O-Methyltectorigenin)

PDB for NP0051472 (4'-O-Methyltectorigenin)

3D PDB for NP0051472 (4'-O-Methyltectorigenin)

SMILES for NP0051472 (4'-O-Methyltectorigenin)

INCHI for NP0051472 (4'-O-Methyltectorigenin)

Structure for NP0051472 (4'-O-Methyltectorigenin)

3D Structure for NP0051472 (4'-O-Methyltectorigenin)