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合成及某些季铵盐氯化物的抗菌活性。

Synthesis and antimicrobial activities of some quaternary morpholinium chlorides.

机构信息

Faculty of Chemistry, Adam Mickiewicz University, Poznań, Poland.

出版信息

Pol J Microbiol. 2010;59(1):49-53.

PMID:20568530
Abstract

The synthesis and antimicrobial activity of 31 morpholinium chlorides, divided into five series depending on the substituents attached to the nitrogen atom, N-carboxyalkyl-morpholinium chlorides (1a-e), N-carbalkoxymethyl-N-methyl-morpholinium chlorides (2a-f), N-carbethoxymethyl-N-alkyl-morpholinium chlorides (3a-g), N-carbalkoxymethyl-N-dodecyl-morpholinium chlorides (4a-f) and N-carboxymethyl-N-alkyl-morpholinium chlorides (5a-g) is reported. The compounds investigated were tested for antimicrobial activity against Staphylococcus aureus, Escherichia coli, Proteus vulgaris, Pseudomonas aeruginosa, Candida albicans and Trichophyton menthagrophytes. The most active are compounds with a long N-alkyl group and with the substituent CH2COOC(n)H(2n-1) (n = 8-16).

摘要

报告了 31 种吗啉𬭩氯化物的合成和抗菌活性,这些氯化物根据连接在氮原子上的取代基分为五个系列:N-羧基烷基吗啉𬭩氯化物(1a-e)、N-羰甲氧甲基-N-甲基吗啉𬭩氯化物(2a-f)、N-羰乙氧甲基-N-烷基吗啉𬭩氯化物(3a-g)、N-羰甲氧甲基-N-十二烷基吗啉𬭩氯化物(4a-f)和 N-羧甲基-N-烷基吗啉𬭩氯化物(5a-g)。研究了这些化合物对金黄色葡萄球菌、大肠杆菌、普通变形杆菌、铜绿假单胞菌、白色念珠菌和须癣毛癣菌的抗菌活性。活性最强的是具有长的 N-烷基基团和取代基 CH2COOC(n)H(2n-1)(n = 8-16)的化合物。

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