Syntheses, in vitro antibacterial and antifungal activities of a series of N-alkyl, 1,4-dithiines

F. Zentz , R. Labia , D. Sirot , O. Faure , R. Grillot , A. Valla
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引用次数: 21

Abstract

A series of dithiines were synthesized by cyclization of 4-(alkylamino)-4-oxobutanoic acids under the action of SOCl2. Their in vitro antibacterial and antifungal activities have been evaluated against reference strains and versus reference compounds. The so-called ‘isoimides’ 2a, 2b were totally inactive whereas some imides had low MICs for few bacteria and for few fungal microorganisms.

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一系列n -烷基,1,4-二硫胺的合成及其体外抗菌和抗真菌活性
在SOCl2的作用下,将4-(烷基胺)-4-氧丁酸环化,合成了一系列二硫胺。对其体外抗菌和抗真菌活性进行了对照菌株和对照化合物的评价。所谓的“异亚胺”2a和2b是完全无活性的,而一些亚胺对少数细菌和真菌微生物具有低mic。
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