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从坦桑尼亚马钱子中分离出的生物碱的抗阿米巴和抗疟活性。

Antiamoebic and antiplasmodial activities of alkaloids isolated from Strychnos usambarensis.

作者信息

Wright C W, Bray D H, O'Neill M J, Warhurst D C, Phillipson J D, Quetin-Leclercq J, Angenot L

机构信息

Department of Pharmacognosy, School of Pharmacy, University of London, U.K.

出版信息

Planta Med. 1991 Aug;57(4):337-40. doi: 10.1055/s-2006-960112.

Abstract

Seven alkaloids isolated from Strychnos usambarensis have been assessed for in vitro activities against Entamoeba histolytica and Plasmodium falciparum and for in vivo activity against Plasmodium berghei in mice. Strychnopentamine and 3',4'-dihydrousambarensine were highly active against P. falciparum in vitro, but were inactive and non-toxic against P. berghei in vivo. Usambarensine, usambarine, and 18,19-dihydrousambarine were highly active against E. histolytica in vitro, but were less active against P. falciparum in vitro. Nb-Methylusambarensine was less active against both protozoa than was usambarensine, and akagerine possessed little antiprotozoal activity. Structure-activity relationships are discussed in the context of the reported cytotoxic and pharmacological properties of these alkaloids.

摘要

从乌干达马钱子(Strychnos usambarensis)中分离出的七种生物碱已被评估其对溶组织内阿米巴(Entamoeba histolytica)和恶性疟原虫(Plasmodium falciparum)的体外活性,以及对小鼠伯氏疟原虫(Plasmodium berghei)的体内活性。士的宁五胺(Strychnopentamine)和3',4'-二氢乌干达马钱子碱(3',4'-dihydrousambarensine)在体外对恶性疟原虫具有高活性,但在体内对伯氏疟原虫无活性且无毒。乌干达马钱子碱(Usambarensine)、乌干达马钱子胺(usambarine)和18,19-二氢乌干达马钱子胺(18,19-dihydrousambarine)在体外对溶组织内阿米巴具有高活性,但在体外对恶性疟原虫的活性较低。Nb-甲基乌干达马钱子碱(Nb-Methylusambarensine)对这两种原生动物的活性均低于乌干达马钱子碱,而阿卡吉林(akagerine)几乎没有抗原生动物活性。结合这些生物碱已报道的细胞毒性和药理特性对构效关系进行了讨论。

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