SYNTHESIS AND ANTIMICROBIAL SCREENING OF N-[2-(2/4-SUBSTITUTED PHENYL)-1-(5/6 SUBSTITUTED 1H- BENZIMIDAZOL-2-YL)VINYL]BENZAMIDES

被引:0
作者
Kaushik, Darpan [1 ]
Khan, Suroor A. [1 ]
Chawla, Gita [1 ]
Panda, Bibhu P. [2 ]
机构
[1] Jamia Hamdard, Div Med Chem, FO Pharm, New Delhi 11062, India
[2] Jamia Hamdard, Microbiol & Biotechnol Div, FO Pharm, New Delhi 11062, India
来源
ACTA POLONIAE PHARMACEUTICA | 2012年 / 69卷 / 04期
关键词
benzimidazole; Erlenmeyer-Plochl azlactone synthesis; identifiable strains; minimal inhibitory concentration; two fold dilution technique; BENZIMIDAZOLE DERIVATIVES; ANTIBACTERIAL ACTIVITY; DESIGN;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A series of (benzamidostyryl)benzimidazole derivatives were synthesized by hydrolyzing 2-phenyl-4-(substituted)benzylidene-5-oxazolones, the azlactone precursors in an acidic medium and treating the product with substituted o-phenylenediamine (OPDA) in situ. The structures of the synthesized compounds were confirmed by spectral and elemental analyses. All synthesized compounds were screened for their in vino antimicrobial activities against some identifiable strains. Thereby, it was found that only nitro substituted benzimidazoles exhibited good to moderate antibacterial activity, while other derivatives were devoid of any antimicrobial effect.
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页码:629 / 636
页数:8
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