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[胺醛缩合物的抗菌活性研究。6. 通讯:取代苯甲醛的偶氮甲碱(作者译)]

[Investigations on the antimicrobial activity of amine-aldehyde-condensates. 6. Communication: azomethines of substituted benzaldehydes (author's transl)].

作者信息

Rehn D, Nolte H

出版信息

Zentralbl Bakteriol B. 1978 Dec;167(5-6):535-45.

PMID:373326
Abstract

In the scope of our research about the antimicrobial activity of amin-aldehydecondensates a number of substituted benzaldehyde azomethines was synthesized by condensation of suitable benzaldehydes with primary amines (aminoethanol and n-butylamine). Structures and physical constants are shown in the table 1. The antimicrobial activity is demonstrated by the results of the disk-test (table 2 and 3), of the minimal inhibition concentration test (MIC, table 4) and of the suspension-disinfecting test following the method of the DGHM (table 5). It may be shown that both the germistatic and the germicidal activity depends on the substituents of the aromatic ring. Bactericidal activity show the test compounds mainly versus the gram-negative bacteria.

摘要

在我们关于氨基醛缩合物抗菌活性的研究范围内,通过合适的苯甲醛与伯胺(氨基乙醇和正丁胺)缩合,合成了许多取代苯甲醛偶氮甲碱。结构和物理常数见表1。抗菌活性通过纸片法试验结果(表2和3)、最低抑菌浓度试验(MIC,表4)以及按照德国卫生与微生物学会(DGHM)方法进行的悬液消毒试验(表5)得以证明。可以看出,抑菌和杀菌活性均取决于芳环上的取代基。测试化合物主要对革兰氏阴性菌表现出杀菌活性。

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