Structure-activity relationship studies of putaminoxins and pinolidoxins: phytotoxic nonenolides produced by phytopathogenic Phoma and Ascochyta species.

A Evidente, R Capasso, A Andolfi, M Vurro, M C Zonno
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引用次数: 37

Abstract

Putaminoxin and pinolidoxin, two structurally related nonenolides, isolated respectively from organic extracts of Phoma putaminum and Aschochyta pinodes cultures, together with some of their natural analogs and synthetic derivatives, were used in a structure-activity relationship study. Their phytotoxic, antifungal and zootoxic activities were assayed with the aim to find compounds with potential herbicidal properties. The strongest phytotoxic compounds proved to be putaminoxin and pinolidoxin, whose activity appeared to be correlated to the integrity of the nonenolide ring and to the presence of both the hydroxy groups and the unmodified propyl side chain. None of the assayed nonenolides showed antifungal activity, whereas pinolidoxin analogs and derivatives showed high to weak zootoxicity.

ptaminoxins和pinolidoxins的构效关系研究:由植物致病性Phoma和Ascochyta种产生的植物毒性nonenolides。
本研究从棕榈叶和松果叶有机提取物中分离得到两种结构相关的非烯内酯类物质:ptaminoxin和pinolidoxin,以及它们的一些天然类似物和合成衍生物,对它们的构效关系进行了研究。对其植物毒性、抗真菌活性和动物毒性进行了测定,以寻找具有潜在除草作用的化合物。最强的植物毒性化合物被证明是果皮毒素和pinolidoxin,其活性似乎与壬烯内酯环的完整性以及羟基和未修饰的丙基侧链的存在有关。所有的非烯内酯均未显示出抗真菌活性,而pinolidoxin类似物和衍生物显示出高到弱的动物毒性。
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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