Synthesis and In Vitro Anticancer Activity of Novel 1,3,4-Oxadiazole-Linked 1,2,3-Triazole/Isoxazole Hybrids

被引:18
|
作者
Madhavilatha, B. [1 ]
Bhattacharjee, Debanjan [2 ]
Sabitha, Gowravaram [1 ,3 ]
Reddy, B. V. Subba [3 ,4 ]
Yadav, J. S. [3 ,4 ]
Jain, Nishant [2 ]
Reddy, B. Jagan Mohan [5 ]
机构
[1] CSIR Indian Inst Chem Technol, Nat Prod Chem Div, Hyderabad 500007, Andhra Pradesh, India
[2] CSIR Indian Inst Chem Technol, Ctr Chem Biol, Hyderabad 500007, Andhra Pradesh, India
[3] Acad Sci & Innovat Res AcSIR, 2 Rafi Marg, New Delhi 110001, India
[4] CSIR Indian Inst Chem Technol, Ctr Semiochem, Hyderabad 500007, Andhra Pradesh, India
[5] Adikavi Nannaya Univ, Dept Chem, Rajahmundry 533296, India
关键词
BIOLOGICAL EVALUATION; ANTIINFLAMMATORY ACTIVITY; SULFONE DERIVATIVES; BEARING OXADIAZOLE; CELL-LINES; MOIETY; AGENTS; INHIBITORS; DESIGN; ANALOGS;
D O I
10.1002/jhet.3110
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of new 1,3,4-oxadiazole-linked 1,2,3-triazole/isoxazole derivatives were designed and synthesized. All the synthesized compounds were screened for in vitro anticancer activity against four human cancer cells: HeLa (cervical), MDA-MB-231 (breast), DU-145 (prostate), and HEPG2 (liver). Among 17 compounds tested, 7a, 7c, and 7d showed potent activity toward four cell lines.
引用
收藏
页码:863 / 870
页数:8
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