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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 SCUTELLAREIN

SMILES

OC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(O)C(O)=C3O

InChI

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

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Inhibition of reverse transcriptases by flavonoids.
1989 Sep
Inhibition of HIV infection by flavanoids.
1993 Oct
Inhibition of HIV activation in latently infected cells by flavonoid compounds.
1996 Jan 1
Inhibitory activity of flavonoids and tannins against HIV-1 protease.
2000 Sep
[Recognition of three classes of skullcaps by FTIR spectroscopy combined with artificial neural networks].
2002 Dec
Ventricular remodeling by Scutellarein treatment in spontaneously hypertensive rats.
2002 Mar
Identification of lipophilic flavones and flavonols by comparative HPLC, TLC and UV spectral analysis.
2003 Mar-Apr
Study on pharmacokinetics of scutellarin in rabbits.
2003 Oct
Variations in lipophilic and vacuolar flavonoids among European Pulicaria species.
2003 Sep
Protection against hydrogen peroxide-induced cytotoxicity in PC12 cells by scutellarin.
2004 Apr 30
Antagonistic effect of scutellarin on the toxicity of selenium in rat livers.
2004 Jun
Separation of flavonoids from the seeds of Vernonia anthelmintica Willd by high-speed counter-current chromatography.
2004 Sep 17
Molecular targets of dietary polyphenols with anti-inflammatory properties.
2005 Oct 31
Determination of aglycone conjugated metabolites of scutellarin in rat plasma by HPLC.
2006 Feb 13
Use of the pig caecum model to mimic the human intestinal metabolism of hispidulin and related compounds.
2006 Jan
[Study on bile excretion of scutellarein].
2006 Oct
Two major urinary metabolites of scutellarin in rats.
2007 Apr
Antioxidant activities of polyphenols extracted from Perilla frutescens varieties.
2008 Dec 31
[Advances in studies on pharmacokinetics of scutellarin and scutellarein].
2009 Dec
Inhibitory effect of flavonoids on 26S proteasome activity.
2009 Oct 28
Anticancer drugs from marine flora: an overview.
2010
[Absorption and transportation characteristics of scutellarin and scutellarein across Caco-2 monolayer model].
2010 Sep
Comparative CYP1A1 and CYP1B1 substrate and inhibitor profile of dietary flavonoids.
2011 May 1
Patents
Name Type Language
SCUTELLAREIN
MI   WHO-DD  
Common Name English
5,6,7-TRIHYDROXY-2-(4-HYDROXYPHENYL)-4H-1-BENZOPYRAN-4-ONE
Systematic Name English
Scutellarein [WHO-DD]
Common Name English
6-HYDROXYAPIGENIN
Common Name English
6-HYDROXYPELARGIDENON-1465
Common Name English
SCUTELLAREIN [MI]
Common Name English
4',5,6,7-TETRAHYDROXYFLAVONE
Systematic Name English
AGLYCONE
Common Name English
Code System Code Type Description
SMS_ID
100000175825
Created by admin on Sat Dec 16 02:24:42 GMT 2023 , Edited by admin on Sat Dec 16 02:24:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID40200946
Created by admin on Sat Dec 16 02:24:42 GMT 2023 , Edited by admin on Sat Dec 16 02:24:42 GMT 2023
PRIMARY
WIKIPEDIA
SCUTELLAREIN
Created by admin on Sat Dec 16 02:24:42 GMT 2023 , Edited by admin on Sat Dec 16 02:24:42 GMT 2023
PRIMARY
PUBCHEM
5281697
Created by admin on Sat Dec 16 02:24:42 GMT 2023 , Edited by admin on Sat Dec 16 02:24:42 GMT 2023
PRIMARY
MERCK INDEX
m9819
Created by admin on Sat Dec 16 02:24:42 GMT 2023 , Edited by admin on Sat Dec 16 02:24:42 GMT 2023
PRIMARY Merck Index
FDA UNII
P460GTI853
Created by admin on Sat Dec 16 02:24:42 GMT 2023 , Edited by admin on Sat Dec 16 02:24:42 GMT 2023
PRIMARY
CHEBI
78328
Created by admin on Sat Dec 16 02:24:42 GMT 2023 , Edited by admin on Sat Dec 16 02:24:42 GMT 2023
PRIMARY
CHEBI
9062
Created by admin on Sat Dec 16 02:24:42 GMT 2023 , Edited by admin on Sat Dec 16 02:24:42 GMT 2023
PRIMARY
CAS
529-53-3
Created by admin on Sat Dec 16 02:24:42 GMT 2023 , Edited by admin on Sat Dec 16 02:24:42 GMT 2023
PRIMARY