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取代的酞嗪-1(2H)-酮类化合物的合成、生物评价及结构研究,用作抗真菌剂。

Synthesis, bioevaluation and structural study of substituted phthalazin-1(2H)-ones acting as antifungal agents.

机构信息

Pharmacognosy Department, Faculty of Biochemical and Pharmaceutical Sciences, National University of Rosario, Suipacha 531, 2000 Rosario, Argentine.

出版信息

Molecules. 2013 Mar 18;18(3):3479-501. doi: 10.3390/molecules18033479.

Abstract

Twenty-five polysubstituted phthalazinone derivatives were synthesized and tested for their antifungal activity against a panel of pathogenic and clinically important yeasts and filamentous fungi. Among them, the compound 4-(4-chlorobenzyl)-2-methylphthalazin-1(2H)-one (5) exhibited a remarkable antifungal activity against standardised strains of dermatophytes and Cryptococcus neoformans, as well as against some clinical isolates. A physicochemical study performed on compound 5 revealed its conformational and electronic characteristics, providing us with useful data for the future design of novel related antifungal analogues.

摘要

合成了 25 种多取代的酞嗪酮衍生物,并测试了它们对一系列致病性和临床上重要的酵母和丝状真菌的抗真菌活性。其中,化合物 4-(4-氯苄基)-2-甲基酞嗪-1(2H)-酮(5)对标准的皮肤真菌和新型隐球菌以及一些临床分离株表现出显著的抗真菌活性。对化合物 5 进行的物理化学研究揭示了其构象和电子特性,为我们未来设计新型相关抗真菌类似物提供了有用的数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0926/6270128/d32ea6b951a1/molecules-18-03479-g004.jpg

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