SYNTHESIS, CHARACTERIZATION AND IN VITRO ANTICANCER EVALUATION OF BIS-[1,5]-BENZOTHIAZEPINES AGAINST HUMAN BREAST CANCER CELL LINE MCF-7

被引:4
|
作者
Deshmukh, R. N. [1 ]
Dengle, R. V. [2 ]
机构
[1] Bharati Vidyapeeth Coll Engn, Kolhapur 416004, Maharashtra, India
[2] Vivekanand Coll, Dept Chem, Kolhapur 416003, Maharashtra, India
关键词
2-aminobenzenethiol; bis-chalcone; 1,5-benzothiazepine; anticancer;
D O I
10.13040/IJPSR.0975-8232.7(12).5024-29
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Bis-[1,5]-benzothiazepines (3a-i) containing two 1,5-benzothiazepine nuclei in a single molecule were synthesized by cyclocondensation reaction of bis-chalcones (1a-i) with two equivalent of 2-aminobenzenethiol (2). All the synthesized compounds were characterized by IR, H-1 NMR, C-13 NMR and mass spectral analysis. Anticancer activity of the synthesized compounds against human breast cancer cell line MCF-7 was determined and the compound (3c) showed significant activity comparable to 5-fluorouracil.
引用
收藏
页码:5024 / 5029
页数:6
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