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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=C(C(O)=C1)C2=COC3=C(C(O)=CC(O)=C3)C2=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

Molecular Formula C15H10O6
Molecular Weight 286.2363
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
LC-MSMS profiling of flavonoid conjugates in wild Mexican lupine, Lupinus reflexus.
2010-07-23
Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa.
2010-07
2'-hydroxylation of genistein enhanced antioxidant and antiproliferative activities in mcf-7 human breast cancer cells.
2009-11
Isoflavonoids from Flemingia strobilifera (L) R. Br. roots.
2009-08-04
Transcript and proteomic analysis of developing white lupin (Lupinus albus L.) roots.
2009-01-05
[Chemical constituents from Spatholobus sinensis].
2008-01
Comparison of plants used for skin and stomach problems in Trinidad and Tobago with Asian ethnomedicine.
2007-01-05
Profiling isoflavone conjugates in different organs of Lupinus exaltatus Zucc.
2006-06-06
Profiling isoflavone conjugates in root extracts of lupine species with LC/ESI/MSn systems.
2005-08
Flavonoids of Crotalaria sessiliflora.
2004-05
Anti-inflammatory flavonoids and pterocarpanoid from Crotalaria pallida and C. assamica.
2004-02-23
Antiplasmodial constituents of Cajanus cajan.
2004-02
Identification of CYP1A2 as the main isoform for the phase I hydroxylated metabolism of genistein and a prodrug converting enzyme of methylated isoflavones.
2003-07
Profiling of flavonoid conjugates in Lupinus albus and Lupinus angustifolius responding to biotic and abiotic stimuli.
2003-05
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:09:15 GMT 2025
Edited
by admin
on Mon Mar 31 19:09:15 GMT 2025
Record UNII
1R3U5726T2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2',4',5,7-TETRAHYDROXYISOFLAVONE
Preferred Name English
2'-HYDROXYGENISTEIN
Common Name English
ISOFLAVONE, 2',4',5,7-TETRAHYDROXY-
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 Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
CAS
1156-78-1
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
EPA CompTox
DTXSID80151145
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
CHEBI
140306
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
PUBCHEM
5282074
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY
FDA UNII
1R3U5726T2
Created by admin on Mon Mar 31 19:09:15 GMT 2025 , Edited by admin on Mon Mar 31 19:09:15 GMT 2025
PRIMARY