Synthesis and Antibacterial Activity Evaluation of Imidazole Derivatives Containing 6‐Methylpyridine Moiety

Author:

Xu Wen‐Bo1,Meng Yu‐Qing1,Sun Jingxin2ORCID,Yang Yu‐Xuan2,Li Wan‐Xin2,Wang Man‐Yu2,Piao Ming‐Guan2,Li Siqi2,Quan Jishan21,Jin Cheng‐Hua21ORCID

Affiliation:

1. Interdisciplinary Program of Biological Function Molecules College of Integration Science Yanbian University Yanji 133002 China

2. Key Laboratory of Natural Medicines of the Changbai Mountain Ministry of Education College of Pharmacy Yanbian University Yanji 133002 China

Abstract

AbstractA series of 2‐cyclopropyl‐5‐(5‐(6‐methylpyridin‐2‐yl)‐2‐substituted‐1H‐imidazol‐4‐yl)‐6‐phenylimidazo[2,1‐b][1,3,4]thiadiazoles (15at and 16af) were synthesized and their antibacterial activities were evaluated. More than half of the compounds showed moderate or strong antibacterial activity. Among them, compounds 15t (MIC=1–2 μg/mL) and 16d (MIC=0.5 μg/mL) showed the strongest antibacterial activities. Notably, compound 16d did not exhibit cytotoxicity in HepG2 cells and did not show hemolysis like the positive control compound Gatifloxacin. The results suggest that compound 16d should be further investigated as a candidate antibacterial agent.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering

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