Microwave-Assisted Synthesis of Methylenebis(phenyl-1H-1,2,3-triazol-5-yl-1,3-thiazolidinones) as Potential Anticancer Agents

被引:2
作者
Srinivas, A. [1 ]
Rajitha, S. R. [2 ]
Suresh, P. D. [3 ]
机构
[1] Vaagdevi Coll Ramnagar, Res & Dev Div, Hanamkonda 506001, India
[2] Carrier Point Univ, Sch Sci, Kota 325003, India
[3] Vaagdevi Degree & PG Coll, Dept Zool, Hanamkonda 506001, India
关键词
hybrid heterocycles; microwave irradiation; click-reaction; thiazolidinones; triazoles; anticancer activity; MULTICOMPONENT REACTIONS; CHEMISTRY; 4-THIAZOLIDINONES; THIAZOLIDIN-4-ONES; DESIGN; ACID;
D O I
10.1134/S1070363223050213
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of hybrid heterocycles was synthesized from methylenebis(thiazolidinone carboxylic acids) by treating with propargyl bromide and p-chlorophenyl azide under microwave irradiation at 65 & DEG;C by using glucose as catalyst. Anticancer activity of the prepared compounds was evaluated by in vitro screening technique against different cancer cell lines DU145, A549, HELA, MCF. Compounds with the 4-Cl, 4-NO2, 4-F, and 4-CH3 groups showed significant anticancer activity against all cell lines examined.
引用
收藏
页码:1201 / 1209
页数:9
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