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Phytochemistry ; 56(2): 189-93, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11219813

ABSTRACT

Two new polyphenolic compounds, myricetin 3-O-(2"-O-galloyl)-beta-D-glucopyranoside and (-)-6-chloroepicatechin, were isolated from the aerial parts of Geranium pratense subsp. finitimum (Woronow) Knuth, along with three known polyphenolic compounds [quercetin 3-O-(2"-O-galloyl)-beta-D-glucopyranoside, quercetin 3-O-(2"-O-galloyl)-beta-D-galactopyranoside, methyl gallate] and tryptophan. Quercetin 3-O-beta-D-glucopyranoside, quercetin 3-O-beta-D-galactopyranoside, quercetin 3-O-(2"-O-galloyl)-beta-D-glucopyranoside and quercetin 3-O-(2"-O-galloyl)-beta-D-galactopyranoside were found to be effective against free radical induced impairment of endothelium-dependent relaxation in isolated rat aorta.


Subject(s)
Catechin/isolation & purification , Free Radical Scavengers/isolation & purification , Glycosides/isolation & purification , Rosales/chemistry , Animals , Catechin/analogs & derivatives , Catechin/chemistry , Catechin/pharmacology , Endothelium, Vascular/drug effects , Endothelium, Vascular/physiology , Free Radical Scavengers/chemistry , Free Radical Scavengers/pharmacology , Glycosides/chemistry , Glycosides/pharmacology , In Vitro Techniques , Male , Molecular Structure , Muscle Relaxation/drug effects , Rats , Spectrum Analysis
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