Synthesis and evaluation of novel marine bromopyrrole alkaloid-based hybrids as anticancer agents

被引:32
作者
Rane, Rajesh A. [1 ]
Sahu, Niteshkumar U. [1 ]
Gutte, Shweta D. [1 ]
Mahajan, Anand A. [1 ]
Shah, Chetan P. [1 ]
Bangalore, Pavankumar [1 ]
机构
[1] NMIMS Univ, SPP Sch Pharm & Technol Management, Bombay 400056, Maharashtra, India
关键词
Marine bromopyrrole alkaloids; Chalcones; Anticancer agent; BIOLOGICAL EVALUATION; IN-VITRO; DERIVATIVES; CHALCONES; CYTOTOXICITY; APOPTOSIS;
D O I
10.1016/j.ejmech.2013.03.029
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of twenty three novel hybrids of marine bromopyrrole alkaloids with chalcone, isoxazole and flavone structural features were synthesized and evaluated for in vitro anticancer activity by MTT assay against five human cancer cell lines. Among the synthesized chalcones, hybrids 4a and 4h (IC50 range: 0.18 mu M-12.00 mu M) showed anticancer activity against all the tested cancer cell lines. Promising cytotoxic activities were exhibited by flavones derivatives, 5a and 5b (0.41 mu M-1.28 mu M) against cell lines PA1 and KB403. Isoxazole hybrids, 6b-6e selectively inhibited oral and mouth cancer cell line KB403, among which 6c (IC50 = 2.45 mu M) was found to be most active. (C) 2013 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:793 / 799
页数:7
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