NP-MRD: Showing NP-Card for 6,7,4'-Trihydroxyisoflavone (NP0044150)

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Record Information

Version

1.0

Created at

2021-11-12 23:52:47 UTC

Updated at

2024-04-19 09:25:09 UTC

NP-MRD ID

NP0044150

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6,7,4'-Trihydroxyisoflavone

Description

6-Hydroxydaidzein, also known as demethyltexasin or soybean factor 2, belongs to the class of organic compounds known as isoflavones. These are polycyclic compounds containing a 2-isoflavene skeleton which bears a ketone group at the C4 carbon atom. Thus, 6-hydroxydaidzein is considered to be a flavonoid lipid molecule. 6-Hydroxydaidzein is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Outside of the human body, 6-Hydroxydaidzein has been detected, but not quantified in, pulses and soy beans. This could make 6-hydroxydaidzein a potential biomarker for the consumption of these foods. 6,7,4'-Trihydroxyisoflavone is found in Centrosema haitiense, Taxus fuana and Taxus yunnanensis. It was first documented in 1999 (PMID: 10540753). A hydroxyisoflavone that is daidzein bearing an additional hydroxy substituent at position 6 (PMID: 15914921) (PMID: 12784638) (PMID: 15215607) (PMID: 16372328).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 30 32  0  0  0  0  0  0  0  0999 V2000
    0.1653    1.0593    1.3647 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2914    0.4025    0.3947 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5581   -0.3186   -0.4197 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9833   -0.3561   -0.2060 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6363    0.8318    0.0631 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0093    0.8360    0.2747 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7086   -0.3578    0.2127 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0957   -0.2915    0.4353 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0758   -1.5532   -0.0543 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6991   -1.5333   -0.2631 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0294   -1.0407   -1.4911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2669   -1.0385   -1.7284 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1319   -0.3776   -0.9980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4877   -0.3687   -1.2374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3188    0.3541   -0.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6862    0.3785   -0.6379 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8422    1.0872    0.6592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7275    1.7984    1.4537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4923    1.0795    0.8992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6325    0.3571    0.0849 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1085    1.7654    0.1145 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5288    1.7721    0.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4806   -0.3877    1.3695 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6535   -2.4616   -0.0945 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2258   -2.4713   -0.4691 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7140   -1.5977   -2.1149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8730   -0.9309   -2.0668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1239   -0.1123   -1.3808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7137    1.8288    1.3117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0841    1.6469    1.7397 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  6  2  0
  6  7  1  0
  7  9  2  0
  9 10  1  0
 10  4  2  0
  4  3  1  0
  3 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 17  2  0
 17 19  1  0
 19 20  2  0
 20  2  1  0
  2  1  2  0
 17 18  1  0
 15 16  1  0
  7  8  1  0
  4  5  1  0
  2  3  1  0
 20 13  1  0
  5 21  1  0
  6 22  1  0
  9 24  1  0
 10 25  1  0
 11 26  1  0
 14 27  1  0
 19 30  1  0
 18 29  1  0
 16 28  1  0
  8 23  1  0
M  END


  Mrv1652311132100522D          

 20 22  0  0  0  0            999 V2000
    0.0000   -2.4750    0.0000 C   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
    0.0000   -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
    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
    2.8579    0.0000    0.0000 C   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
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   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
    4.2868   -0.0000    0.0000 O   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
  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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  2  0  0  0  0
 13 18  1  0  0  0  0
 12 19  1  0  0  0  0
  3 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0044150

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1)C1=COC2=CC(O)=C(O)C=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)11-7-20-14-6-13(18)12(17)5-10(14)15(11)19/h1-7,16-18H

> <INCHI_KEY>
GYLUFQJZYAJQDI-UHFFFAOYSA-N

> <FORMULA>
C15H10O5

> <MOLECULAR_WEIGHT>
270.2369

> <EXACT_MASS>
270.05282343

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
26.719903691855013

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one

> <ALOGPS_LOGP>
3.08

> <JCHEM_LOGP>
2.4268723896666664

> <ALOGPS_LOGS>
-3.37

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.964574881342447

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.582051557346977

> <JCHEM_PKA_STRONGEST_BASIC>
-5.322125573061659

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
71.6829

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.14e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-hydroxydaidzein

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 13-NOV-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   13-NOV-21         0                                  
HETATM    1  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   19                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   10   16                                                  
CONECT   16   15    7   17                                                  
CONECT   17   16                                                            
CONECT   18   13                                                            
CONECT   19   12                                                            
CONECT   20    3                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

View in JSmol

Synonyms

Value	Source
6,7,4'-Trihydroxyisoflavone	ChEBI
6,7-Dihydroxy-3-(4-hydroxy-phenyl)-chromen-4-one	HMDB
6,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one, 9ci	HMDB
6,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one	HMDB
Demethyltexasin	HMDB
Soybean factor 2	HMDB
6-Hydroxydaidzein	ChEBI

Chemical Formula

C₁₅H₁₀O₅

Average Mass

270.2369 Da

Monoisotopic Mass

270.05282 Da

IUPAC Name

6,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one

Traditional Name

6-hydroxydaidzein

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1)C1=COC2=CC(O)=C(O)C=C2C1=O

InChI Identifier

InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)11-7-20-14-6-13(18)12(17)5-10(14)15(11)19/h1-7,16-18H

InChI Key

GYLUFQJZYAJQDI-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Centrosema haitiense	Plant	KNApSAcK
Glycine max	FooDB	Dr. Duke's Phytochemical and Ethnobotanical Databases
Taxus fuana	Plant	KNApSAcK
Taxus wallichiana var. yunnanensis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoflavones. These are polycyclic compounds containing a 2-isoflavene skeleton which bears a ketone group at the C4 carbon atom.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Isoflav-2-enes

Direct Parent

Isoflavones

Alternative Parents

Substituents

Isoflavone
Hydroxyisoflavonoid
Chromone
Benzopyran
1-benzopyran
Pyranone
Phenol
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Pyran
Heteroaromatic compound
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

7-hydroxyisoflavones (CHEBI:74957 )
Isoflavonoids (LMPK12050102 )
a small molecule (CPD-6998 )

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	3.08	ALOGPS
logP	2.43	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	6.58	ChemAxon
pKa (Strongest Basic)	-5.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	71.68 m³·mol⁻¹	ChemAxon
Polarizability	26.72 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

HMDB0031715

DrugBank ID

Not Available

Phenol Explorer Compound ID

FoodDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5284649

PDB ID

Not Available

ChEBI ID

74957

Good Scents ID

Not Available

References

General References

Chen YC, Sugiyama Y, Abe N, Kuruto-Niwa R, Nozawa R, Hirota A: DPPH radical-scavenging compounds from dou-chi, a soybean fermented food. Biosci Biotechnol Biochem. 2005 May;69(5):999-1006. doi: 10.1271/bbb.69.999. [PubMed:15914921 ]
Esaki H, Kawakishi S, Morimitsu Y, Osawa T: New potent antioxidative o-dihydroxyisoflavones in fermented Japanese soybean products. Biosci Biotechnol Biochem. 1999 Sep;63(9):1637-9. doi: 10.1271/bbb.63.1637. [PubMed:10540753 ]
Chen YC, Inaba M, Abe N, Hirota A: Antimutagenic activity of 8-hydroxyisoflavones and 6-hydroxydaidzein from soybean miso. Biosci Biotechnol Biochem. 2003 Apr;67(4):903-6. doi: 10.1271/bbb.67.903. [PubMed:12784638 ]
Hirota A, Inaba M, Chen YC, Abe N, Taki S, Yano M, Kawaii S: Isolation of 8-hydroxyglycitein and 6-hydroxydaidzein from soybean miso. Biosci Biotechnol Biochem. 2004 Jun;68(6):1372-4. doi: 10.1271/bbb.68.1372. [PubMed:15215607 ]
Hedlund TE, van Bokhoven A, Johannes WU, Nordeen SK, Ogden LG: Prostatic fluid concentrations of isoflavonoids in soy consumers are sufficient to inhibit growth of benign and malignant prostatic epithelial cells in vitro. Prostate. 2006 Apr 1;66(5):557-66. doi: 10.1002/pros.20380. [PubMed:16372328 ]
Te-Sheng Chang, Hsiou-Yu Ding, Sorgan Shou-Ku Tai, Ching-Yi Wu (2007). Mushroom tyrosinase inhibitory effects of isoflavones isolated from soygerm koji fermented with Aspergillus oryzae BCRC 32288. Food Chemistry, Volume 105, Issue 4, 2007, Pages 1430-1438. DOI: 10.1016/j.foodchem.2007.05.019. Food Chemistry.

Showing NP-Card for 6,7,4'-Trihydroxyisoflavone (NP0044150)

MOL for NP0044150 (6,7,4'-Trihydroxyisoflavone)

3D MOL for NP0044150 (6,7,4'-Trihydroxyisoflavone)

3D SDF for NP0044150 (6,7,4'-Trihydroxyisoflavone)

3D-SDF for NP0044150 (6,7,4'-Trihydroxyisoflavone)

PDB for NP0044150 (6,7,4'-Trihydroxyisoflavone)

3D PDB for NP0044150 (6,7,4'-Trihydroxyisoflavone)

SMILES for NP0044150 (6,7,4'-Trihydroxyisoflavone)

INCHI for NP0044150 (6,7,4'-Trihydroxyisoflavone)

Structure for NP0044150 (6,7,4'-Trihydroxyisoflavone)

3D Structure for NP0044150 (6,7,4'-Trihydroxyisoflavone)