N-Arylidene-4-(4-nitro-1H-benzo[d]imidazol-2-yl)aniline Derivatives as Antimycobacterial Agents

被引:0
作者
Alsaiari, Ahad Amer [1 ]
Almehmadi, Mazen M. [1 ]
Asif, Mohammad [2 ]
机构
[1] Taif Univ, Coll Appl Med Sci, Dept Clin Lab Sci, POB 11099, Taif 21944, Saudi Arabia
[2] Glocal Univ, Sch Pharm, Saharanpur 247121, Uttar Pradesh, India
来源
LATIN AMERICAN JOURNAL OF PHARMACY | 2023年 / 42卷 / 03期
关键词
ly drug -resistant (XDR); multi; -drug; -resistant; KEY WORDS; antitubercular agent; benzimidazole; heterocyclic; synthesis;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A series of novel N-Arylidene-4-(4-nitro-1H-benzo[d]imidazol-2-yl)aniline derivatives (2a-e) were designed and synthesized from 3-nitro-1,2diphenylenediamine and p-aminobenzoic acid followed by reacted with appropriate aromatic aldehydes to formed final compounds (Schiff's base). All the title compounds were characterized by FT-IR, 1H-NMR, and Mass spectroscopy. In vitro antimycobacterial activity by using the Microplate Alamar Blue dye Assay (MABA) technique against M. tuberculosis H37Rv method was performed. According to the findings of biological research, all of the compounds in the title displayed weak antimycobacterial action. The biological activity of the screened compounds and the functional group variation were related, and this was discussed.
引用
收藏
页码:562 / 566
页数:5
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