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Details

Stereochemistry ACHIRAL
Molecular Formula C16H12O7
Molecular Weight 316.2623
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TAMARIXETIN

SMILES

COC1=CC=C(C=C1O)C2=C(O)C(=O)C3=C(O2)C=C(O)C=C3O

InChI

InChIKey=FPLMIPQZHHQWHN-UHFFFAOYSA-N
InChI=1S/C16H12O7/c1-22-11-3-2-7(4-9(11)18)16-15(21)14(20)13-10(19)5-8(17)6-12(13)23-16/h2-6,17-19,21H,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Endothelium-independent vasodilator effects of the flavonoid quercetin and its methylated metabolites in rat conductance and resistance arteries.
2002 Jul
In vitro investigation of cytochrome P450-mediated metabolism of dietary flavonoids.
2002 May
Ginkgo biloba extract EGb 761 increases stress resistance and extends life span of Caenorhabditis elegans.
2002 Sep
Kinetic and stoichiometric assessment of the antioxidant activity of flavonoids by electron spin resonance spectroscopy.
2003 Mar 12
Intracellular metabolism and bioactivity of quercetin and its in vivo metabolites.
2003 May 15
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
Inhibition of human cytochromes P450 by components of Ginkgo biloba.
2004 Aug
Molecular characterization and functional expression of flavonol 6-hydroxylase.
2004 Dec 13
The type of sugar moiety is a major determinant of the small intestinal uptake and subsequent biliary excretion of dietary quercetin glycosides.
2004 Jun
Consequences of quercetin methylation for its covalent glutathione and DNA adduct formation.
2006 Apr 15
The reaction of flavonoid metabolites with peroxynitrite.
2006 Dec 1
Determination of St. John's wort flavonoid-metabolites in rat brain through high performance liquid chromatography coupled with fluorescence detection.
2006 Feb 17
TCDD-induced CYP1A1 expression, an index of dioxin toxicity, is suppressed by flavonoids permeating the human intestinal Caco-2 cell monolayers.
2006 Nov 15
Ingestion of onion soup high in quercetin inhibits platelet aggregation and essential components of the collagen-stimulated platelet activation pathway in man: a pilot study.
2006 Sep
Role of quercetin and its in vivo metabolites in protecting H9c2 cells against oxidative stress.
2007 Jan
[Studies on flavonoids from Blumea riparia].
2008 Apr
St. John's wort flavonoids and their metabolites show antidepressant activity and accumulate in brain after multiple oral doses.
2008 Apr
Antioxidant activity and metabolite profile of quercetin in vitamin-E-depleted rats.
2008 Jul
Glial metabolism of quercetin reduces its neurotoxic potential.
2008 Oct 15
Bioactive terpenoids and flavonoids from Ginkgo biloba extract induce the expression of hepatic drug-metabolizing enzymes through pregnane X receptor, constitutive androstane receptor, and aryl hydrocarbon receptor-mediated pathways.
2009 Apr
A new ferulic acid ester and other constituents from Tamarix nilotica leaves.
2009 Jul
Aphyllin, the first isoferulic acid glycoside and other phenolics from Tamarix aphylla flowers.
2009 May
Flavonoids and isoflavonoids from Sophorae Flos improve glucose uptake in vitro.
2010 Jan
A structural basis for the inhibition of collagen-stimulated platelet function by quercetin and structurally related flavonoids.
2010 Mar
Free fruit at workplace intervention increases total fruit intake: a validation study using 24 h dietary recall and urinary flavonoid excretion.
2010 Oct
Name Type Language
TAMARIXETIN
Common Name English
4H-1-BENZOPYRAN-4-ONE, 3,5,7-TRIHYDROXY-2-(3-HYDROXY-4-METHOXYPHENYL)-
Systematic Name English
4'-O-METHYLQUERCETIN
Common Name English
3,3',5,7-TETRAHYDROXY-4'-METHOXYFLAVONE
Systematic Name English
QUERCETIN 4'-METHYL ETHER
Common Name English
Code System Code Type Description
CHEBI
67492
Created by admin on Fri Dec 15 17:55:02 GMT 2023 , Edited by admin on Fri Dec 15 17:55:02 GMT 2023
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EPA CompTox
DTXSID00209056
Created by admin on Fri Dec 15 17:55:02 GMT 2023 , Edited by admin on Fri Dec 15 17:55:02 GMT 2023
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PUBCHEM
5281699
Created by admin on Fri Dec 15 17:55:02 GMT 2023 , Edited by admin on Fri Dec 15 17:55:02 GMT 2023
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ECHA (EC/EINECS)
210-050-7
Created by admin on Fri Dec 15 17:55:02 GMT 2023 , Edited by admin on Fri Dec 15 17:55:02 GMT 2023
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CAS
603-61-2
Created by admin on Fri Dec 15 17:55:02 GMT 2023 , Edited by admin on Fri Dec 15 17:55:02 GMT 2023
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FDA UNII
73WRA8Z8M8
Created by admin on Fri Dec 15 17:55:02 GMT 2023 , Edited by admin on Fri Dec 15 17:55:02 GMT 2023
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WIKIPEDIA
TAMARIXETIN
Created by admin on Fri Dec 15 17:55:02 GMT 2023 , Edited by admin on Fri Dec 15 17:55:02 GMT 2023
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