Bifunctional ethyl 2-amino-4-methylthiazole-5-carboxylate derivatives: Synthesis and in vitro biological evaluation as antimicrobial and anticancer agents

被引:54
|
作者
Rostom, Sherif A. F. [1 ,2 ]
Faidallah, Hassan M. [3 ]
Radwan, Mohammed F. [1 ,4 ]
Badr, Mona H. [1 ,2 ]
机构
[1] King Abdulaziz Univ, Dept Pharmaceut Chem, Fac Pharm, Jeddah 21589, Saudi Arabia
[2] Univ Alexandria, Fac Pharm, Dept Pharmaceut Chem, Alexandria 21521, Egypt
[3] King Abdulaziz Univ, Dept Chem, Fac Sci, Jeddah 21589, Saudi Arabia
[4] Menia Univ, Dept Med Chem, Fac Pharm, Menia 61519, Egypt
关键词
Synthesis; Thiazoles; Antibacterial; Antifungal; Anticancer; THIAZOLE DERIVATIVES; ANTITUMOR AGENTS; INHIBITORS; DISCOVERY; ANTIBACTERIAL; ANALOGS; CELLS; SULFONAMIDES; SYSTEMS; DESIGN;
D O I
10.1016/j.ejmech.2014.02.027
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Thirty thiazole compounds bearing chemotherapeutically-active pharmacophores were synthesized and evaluated for their preliminary in vitro antimicrobial and anticancer activities. Nineteen compounds displayed obvious antibacterial potential, with special bactericidal activity against Gram positive bacteria, whereas, nine analogs showed moderate to weak antifungal activity against Candida albicans. The analog 12f proved to be the most active antimicrobial member identified in this study being comparable to ampicillin and gentamicin sulfate against Staphylococcus aureus and Bacillus subtilis, together with a moderate antifungal activity. Additionally, nine derivatives were tested for their preliminary in vitro anticancer activity according to the current one-dose protocol of the NCI. Compound 9b revealed a broad spectrum of anticancer activity against 29 out of the tested 60 subpanel tumor cell lines. Collectively, compounds 4, 9b, 10b and 12f could be considered as promising dual anticancer antibiotics. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:170 / 181
页数:12
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