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Details

Stereochemistry ACHIRAL
Molecular Formula C15H10O6
Molecular Weight 286.2363
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2'-HYDROXYGENISTEIN

SMILES

OC1=CC(O)=C(C=C1)C2=COC3=CC(O)=CC(O)=C3C2=O

InChI

InChIKey=GSSOWCUOWLMMRJ-UHFFFAOYSA-N
InChI=1S/C15H10O6/c16-7-1-2-9(11(18)3-7)10-6-21-13-5-8(17)4-12(19)14(13)15(10)20/h1-6,16-19H

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Antiplasmodial constituents of Cajanus cajan.
2004 Feb
Profiling isoflavone conjugates in root extracts of lupine species with LC/ESI/MSn systems.
2005 Aug
Profiling isoflavone conjugates in different organs of Lupinus exaltatus Zucc.
2006 May-Jun
Transcript and proteomic analysis of developing white lupin (Lupinus albus L.) roots.
2009 Jan 5
LC-MSMS profiling of flavonoid conjugates in wild Mexican lupine, Lupinus reflexus.
2010 Jul 23
Patents

Patents

Name Type Language
2'-HYDROXYGENISTEIN
Common Name English
ISOFLAVONE, 2',4',5,7-TETRAHYDROXY-
Common Name English
2',4',5,7-TETRAHYDROXYISOFLAVONE
Common Name English
4H-1-BENZOPYRAN-4-ONE, 3-(2,4-DIHYDROXYPHENYL)-5,7-DIHYDROXY-
Systematic Name English
2'-HYDROXYISOPRUNETIN
Common Name English
Code System Code Type Description
CHEBI
70031
Created by admin on Fri Dec 15 18:17:15 GMT 2023 , Edited by admin on Fri Dec 15 18:17:15 GMT 2023
PRIMARY
CAS
1156-78-1
Created by admin on Fri Dec 15 18:17:15 GMT 2023 , Edited by admin on Fri Dec 15 18:17:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID80151145
Created by admin on Fri Dec 15 18:17:15 GMT 2023 , Edited by admin on Fri Dec 15 18:17:15 GMT 2023
PRIMARY
CHEBI
140306
Created by admin on Fri Dec 15 18:17:15 GMT 2023 , Edited by admin on Fri Dec 15 18:17:15 GMT 2023
PRIMARY
PUBCHEM
5282074
Created by admin on Fri Dec 15 18:17:15 GMT 2023 , Edited by admin on Fri Dec 15 18:17:15 GMT 2023
PRIMARY
FDA UNII
1R3U5726T2
Created by admin on Fri Dec 15 18:17:15 GMT 2023 , Edited by admin on Fri Dec 15 18:17:15 GMT 2023
PRIMARY