ERIODICTYOL

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C15H12O6
Molecular Weight	288.2522
Optical Activity	UNSPECIFIED
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OC1=CC2=C(C(=O)C[C@H](O2)C3=CC(O)=C(O)C=C3)C(O)=C1

InChI

InChIKey=SBHXYTNGIZCORC-ZDUSSCGKSA-N

InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2/t13-/m0/s1

HIDE SMILES / InChI

Approval Year

PubMed

Title	Date	PubMed
Determination of phenolic compounds in rose hip (Rosa canina) using liquid chromatography coupled to electrospray ionisation tandem mass spectrometry and diode-array detection.	2002	11921243
Flavonoids suppress the cytotoxicity of linoleic acid hydroperoxide toward PC12 cells.	2002 Aug	12186416
Antioxidant chalcone glycosides and flavanones from Maclura (Chlorophora) tinctoria.	2003 Aug	12932124
Separation of some chiral flavanones by micellar electrokinetic chromatography.	2003 Aug	12900864
The splanchnic metabolism of flavonoids highly differed according to the nature of the compound.	2003 Jun	12736148
Free radical scavenging abilities of flavonoids as mechanism of protection against mutagenicity induced by tert-butyl hydroperoxide or cumene hydroperoxide in Salmonella typhimurium TA102.	2003 Sep 9	12972054
Inhibitory effects of flavonoids on phosphodiesterase isozymes from guinea pig and their structure-activity relationships.	2004 Nov 15	15476679
Flavonoids as chemotaxonomic markers for Erythroxylum australe.	2004 Nov-Dec	15666532
The pig caecum model: a suitable tool to study the intestinal metabolism of flavonoids.	2004 Sep	15497184
High-performance liquid chromatographic separation and chiroptical properties of the enantiomers of naringenin and other flavanones.	2005 May 27	15974082
Oxidation of the flavonoid eriodictyol by tyrosinase.	2005 Sep	16289948
Flavonoids protect human retinal pigment epithelial cells from oxidative-stress-induced death.	2006 Jul	16799064
Polar constituents from the aerial parts of Origanum vulgare L. Ssp. hirtum growing wild in Greece.	2006 Jul 26	16848522
Cytotoxic and new tetralone derivatives from Berchemia floribunda (Wall.) Brongn.	2006 Jun	17193298
Characterization of flavonoid 7-O-glucosyltransferase from Arabidopsis thaliana.	2006 Jun	16794327
Triterpenic acids and flavonoids from Satureja parvifolia. Evaluation of their antiprotozoal activity.	2006 Mar-Apr	16729575
Antibacterial phenolic compounds from the spines of Gleditsia sinensis Lam.	2007 Apr	17479415
Protective effects of epigallocatechin gallate after UV irradiation in cultured human retinal pigment epithelial cells.	2007 Dec	18063889
The anti-apoptotic and anti-oxidant effect of eriodictyol on UV-induced apoptosis in keratinocytes.	2007 Jan	17202655
The flavonoid, fisetin, inhibits UV radiation-induced oxidative stress and the activation of NF-kappaB and MAPK signaling in human lens epithelial cells.	2008	18949064
Accumulation of flavonols in response to ultraviolet-B irradiation in soybean is related to induction of flavanone 3-beta-hydroxylase and flavonol synthase.	2008 Apr 30	18414005
Antioxidant aryl-prenylcoumarin, flavan-3-ols and flavonoids from Eysenhardtia subcoriacea.	2008 Jan	17892888
Metabolite annotations based on the integration of mass spectral information.	2008 Jun	18266924
Separation of flavanone enantiomers and flavanone glucoside diastereomers from Balanophora involucrata Hook. f. by capillary electrophoresis and reversed-phase high-performance liquid chromatography on a C18 column.	2008 Mar 21	18291407
Influence of Honey on the Suppression of Human Low Density Lipoprotein (LDL) Peroxidation (In vitro).	2009 Mar	18955249

Patents

Name

Type

Language

ERIODICTYOL

Official Name

English

(S)-3',4',5,7-TETRAHYDROXYFLAVANONE

Systematic Name

English

ERIODICTYOL [INCI]

Common Name

English

(2S)-2-(3,4-DIHYDROXYPHENYL)-2,3-DIHYDRO-5,7-DIHYDROXY-4H-1-BENZOPYRAN-4-ONE

Systematic Name

English

ERIODICTYOL [MI]

Common Name

English

(+)-ERIODICTYOL

Common Name

English

NSC-649412

Code

English

Code System Code Type Description

FDA UNII

Q520486B8Y