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Phytochemistry ; 109: 96-102, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25468714

ABSTRACT

Hispidacine, an 8,4'-oxyneolignan featuring incorporation of an unusual 2-hydroxyethylamine moiety at C-7, and hispiloscine, a phenanthroindolizidine alkaloid, were isolated from the stem-bark and leaves of the Malaysian Ficus hispida Linn. Their structures were established by spectroscopic analysis. Hispidacine induced a moderate vasorelaxant activity in rat isolated aorta, while hispiloscine showed appreciable antiproliferative activities against MDA-MB-231, MCF-7, A549, HCT-116 and MRC-5 cell lines.


Subject(s)
Alkaloids/chemistry , Antineoplastic Agents, Phytogenic/chemistry , Ficus/chemistry , Lignans/chemistry , Vasodilator Agents/chemistry , Alkaloids/isolation & purification , Animals , Antineoplastic Agents, Phytogenic/isolation & purification , Aorta/drug effects , Cell Line, Tumor , Humans , Indolizidines/chemistry , Indolizidines/isolation & purification , Indolizines/chemistry , Indolizines/isolation & purification , Lignans/isolation & purification , Male , Molecular Structure , Phenanthrolines/chemistry , Phenanthrolines/isolation & purification , Plant Bark/chemistry , Plant Leaves/chemistry , Rats, Sprague-Dawley , Vasodilator Agents/isolation & purification
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