Synthesis and antimycobacterial activity of some isonicotinoylhydrazones

被引:58
作者
Cocco, MT
Congiu, C
Onnis, V
Pusceddu, MC
Schivo, ML
De Logu, A
机构
[1] Univ Cagliari, Dipartimento Tossicol, I-09126 Cagliari, Italy
[2] Univ Cagliari, Dipartimento Sci Chirurg & Trapianti Organo, Sez Microbiol & Virol, I-09123 Cagliari, Italy
关键词
aminohydrazone derivatives; synthesis; antimycobacterial activity;
D O I
10.1016/S0223-5234(99)00124-5
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of isonicotinoylhydrazones 2 were prepared by addition of some aryloxyacetonitriles with isonicotinoylhydrazine in basic medium. These compounds have been further reacted with pyridinecarboxaldehydes to give the corresponding pyridylmethyleneamino derivatives 3-5. The new synthesized hydrazones and their pyridylmethyleneamino derivatives were tested for their activity against mycobacteria, Gram-positive and Gram-negative bacteria. The cytotoxicity was also tested. Several compounds showed a good activity against Mycobacterium tuberculosis H37Rv and some isonycotinoylhydrazones 2 showed a moderate activity against a clinically isolated M. tuberculosis which was isoniazid resistant. (C) 1999 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:1071 / 1076
页数:6
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