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Details

Stereochemistry ACHIRAL
Molecular Formula C15H10O4
Molecular Weight 254.2375
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3',4'-DIHYDROXYFLAVONE

SMILES

OC1=CC=C(C=C1O)C2=CC(=O)C3=C(O2)C=CC=C3

InChI

InChIKey=SRNPMQHYWVKBAV-UHFFFAOYSA-N
InChI=1S/C15H10O4/c16-11-6-5-9(7-13(11)18)15-8-12(17)10-3-1-2-4-14(10)19-15/h1-8,16,18H

HIDE SMILES / InChI

Molecular Formula C15H10O4
Molecular Weight 254.2375
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Flavonoids suppress human glioblastoma cell growth by inhibiting cell metabolism, migration, and by regulating extracellular matrix proteins and metalloproteinases expression.
2015-12-05
Characterization of an O-methyltransferase from Streptomyces avermitilis MA-4680.
2010-09
Flavonoid-induced morphological modifications of endothelial cells through microtubule stabilization.
2009
Iron-binding properties of plant phenolics and cranberry's bio-effects.
2007-11-21
Evaluation of novel chromogenic substrates for the detection of bacterial beta-glucosidase.
2007-02
The anti-apoptotic and anti-oxidant effect of eriodictyol on UV-induced apoptosis in keratinocytes.
2007-01
Spectroscopic and theoretical studies of the Zn(II) chelation with hydroxyflavones.
2006-11-16
Influence of biotransformation of luteolin, luteolin 7-O-glucoside, 3',4'-dihydroxyflavone and apigenin by cultured rat hepatocytes on antioxidative capacity and inhibition of EGF receptor tyrosine kinase activity.
2006-06
Time dependent density functional theory study of electronic absorption properties of lead(II) complexes with a series of hydroxyflavones.
2005-08-04
Stability of ferric complexes with 3-hydroxyflavone (flavonol), 5,7-dihydroxyflavone (chrysin), and 3',4'-dihydroxyflavone.
2005-04-20
Quantitative structure activity relationship studies on the flavonoid mediated inhibition of multidrug resistance proteins 1 and 2.
2005-02-15
3',4'-Dihydroxyflavonol reduces infarct size and injury associated with myocardial ischaemia and reperfusion in sheep.
2004-06
The regioselectivity of glutathione adduct formation with flavonoid quinone/quinone methides is pH-dependent.
2002-03
Complexes of Al(III) with 3'4'-dihydroxy-flavone: characterization, theoretical and spectroscopic study.
2001-03-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:56:36 GMT 2025
Edited
by admin
on Mon Mar 31 19:56:36 GMT 2025
Record UNII
KOH101S66V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3',4'-DIHYDROXYFLAVONE
Preferred Name English
Code System Code Type Description
FDA UNII
KOH101S66V
Created by admin on Mon Mar 31 19:56:36 GMT 2025 , Edited by admin on Mon Mar 31 19:56:36 GMT 2025
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CAS
4143-64-0
Created by admin on Mon Mar 31 19:56:36 GMT 2025 , Edited by admin on Mon Mar 31 19:56:36 GMT 2025
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EPA CompTox
DTXSID70194349
Created by admin on Mon Mar 31 19:56:36 GMT 2025 , Edited by admin on Mon Mar 31 19:56:36 GMT 2025
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PUBCHEM
145726
Created by admin on Mon Mar 31 19:56:36 GMT 2025 , Edited by admin on Mon Mar 31 19:56:36 GMT 2025
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MESH
C028288
Created by admin on Mon Mar 31 19:56:36 GMT 2025 , Edited by admin on Mon Mar 31 19:56:36 GMT 2025
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