Synthesis of New 2-N-Substituted Amino-5-aryl-1,3-thiazoles as Antitumor Agents

被引:0
|
作者
Elsayed, Elsherbiny Hamdy [1 ]
Moustafa, Amal Y. [1 ]
El-Ata, Sara A. A. [1 ]
机构
[1] Port Said Univ, Chem Dept, Fac Sci, Port Said, Egypt
来源
LATIN AMERICAN JOURNAL OF PHARMACY | 2018年 / 37卷 / 08期
关键词
cytotoxicity; HepG-2; MCF-7; thiazole; ALPHA-AMINOPHOSPHONATES;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A new 5-aryl-2-N-substituted thiazole derivatives 3a, b were synthesized via the cyclization of thiosemicarbazone 2 with viaries alpha-bromomethyl aryl ketones. Acetylation and alkylation of thiazole derivatives 3a, b with acetic anhydride and ethyl chloroacetate gave the corresponding N-acetyl and N-alkyl derivatives 4 and 5. The structures of the synthesized 1,3- thiazole derivatives 3, 4 and 5 were confirmed by IR, H-1, C-13-NMR, MS and elemental analysis. All the synthesized thiazole derivatives and carbazone were tested for their cytotoxicity against two different cancer cell lines MCF-7 and HepG-2. Some of these compounds showed good cytotoxicity.
引用
收藏
页码:1594 / 1601
页数:8
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