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
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
| 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
| Title | Date | PubMed |
|---|---|---|
| Complexes of Al(III) with 3'4'-dihydroxy-flavone: characterization, theoretical and spectroscopic study. | 2001 Mar 1 |
|
| The regioselectivity of glutathione adduct formation with flavonoid quinone/quinone methides is pH-dependent. | 2002 Mar |
|
| 3',4'-Dihydroxyflavonol reduces infarct size and injury associated with myocardial ischaemia and reperfusion in sheep. | 2004 Jun |
|
| Stability of ferric complexes with 3-hydroxyflavone (flavonol), 5,7-dihydroxyflavone (chrysin), and 3',4'-dihydroxyflavone. | 2005 Apr 20 |
|
| Time dependent density functional theory study of electronic absorption properties of lead(II) complexes with a series of hydroxyflavones. | 2005 Aug 4 |
|
| Quantitative structure activity relationship studies on the flavonoid mediated inhibition of multidrug resistance proteins 1 and 2. | 2005 Feb 15 |
|
| Evaluation of novel chromogenic substrates for the detection of bacterial beta-glucosidase. | 2007 Feb |
|
| The anti-apoptotic and anti-oxidant effect of eriodictyol on UV-induced apoptosis in keratinocytes. | 2007 Jan |
|
| Iron-binding properties of plant phenolics and cranberry's bio-effects. | 2007 Nov 21 |
|
| Flavonoid-induced morphological modifications of endothelial cells through microtubule stabilization. | 2009 |
|
| Characterization of an O-methyltransferase from Streptomyces avermitilis MA-4680. | 2010 Sep |
|
| Flavonoids suppress human glioblastoma cell growth by inhibiting cell metabolism, migration, and by regulating extracellular matrix proteins and metalloproteinases expression. | 2015 Dec 5 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:46:36 GMT 2023
by
admin
on
Fri Dec 15 19:46:36 GMT 2023
|
| Record UNII |
KOH101S66V
|
| Record Status |
Validated (UNII)
|
| Record Version |
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KOH101S66V
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4143-64-0
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DTXSID70194349
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145726
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C028288
Created by
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