Pyrrolizidine Alkaloids.

Q1 Biochemistry, Genetics and Molecular Biology
Alkaloids: Chemistry and Biology Pub Date : 2018-01-01 Epub Date: 2018-07-06 DOI:10.1016/bs.alkal.2018.03.001
Joaquín Tamariz, Eleuterio Burgueño-Tapia, Miguel A Vázquez, Francisco Delgado
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引用次数: 14

Abstract

Naturally occurring pyrrolizidine alkaloids (PAs) are isolated from plants and other sources. The interest of the scientific community in these compounds owes itself to their high toxicity and biological activity, as well as to the challenge of synthesizing their pyrrolizidine scaffold. This review encompasses a wide range of topics found in the literature from 1995 to date, including the occurrence, biosynthesis, toxicity (hepatotoxicity, genotoxicity, and tumorigenicity), biological activity, and pharmacological properties (glycosidase inhibitory activity) of these secondary metabolites. Particular attention is given to the chemistry of PAs, addressing general strategies for formal and total syntheses via amino-based substrates, pyrroles, and pyrrolidine-based derivatives.

Pyrrolizidine生物碱。
天然存在的吡咯利西啶生物碱(PAs)是从植物和其他来源分离出来的。科学界对这些化合物的兴趣在于它们的高毒性和生物活性,以及合成它们的吡咯利西啶支架的挑战。本综述涵盖了从1995年至今的文献中发现的广泛主题,包括这些次生代谢物的发生、生物合成、毒性(肝毒性、遗传毒性和致瘤性)、生物活性和药理学特性(糖苷酶抑制活性)。特别关注PAs的化学,通过氨基底物,吡咯和吡咯烷基衍生物解决正式和全面合成的一般策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Alkaloids: Chemistry and Biology
Alkaloids: Chemistry and Biology Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
13.70
自引率
0.00%
发文量
21
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