A One-pot Facile Construction of 1H-1,2,3-Triazolyl 1,2-Dihydropyridyl Derivatives and Evaluation of Bioactivity Profile

被引:4
|
作者
Rajkumar, Kommera [1 ,4 ]
Murthy, Thampunuri Ramalinga [2 ]
Zehra, Amtul [3 ]
Khursade, Parag Sakharam [1 ]
Kaliyendi, Shasi Vardhan [2 ]
Tiwari, Ashok Kumar [3 ]
Prakasham, Reddy Shetty [1 ]
Raju, Bhimapaka China [1 ,4 ]
机构
[1] CSIR, Indian Inst Chem Technol, Organ Synth & Proc Chem Div, Hyderabad 500007, India
[2] CSIR, Indian Inst Chem Technol, Appl Biol Div, Hyderabad 500007, India
[3] CSIR, Indian Inst Chem Technol, Ctr Nat Prod & Tradit Knowledge, Hyderabad 500007, India
[4] AcSIR Postal Staff Coll Area, Sect 19, Ghaziabad 201002, Uttar Pradesh, India
来源
CHEMISTRYSELECT | 2018年 / 3卷 / 48期
关键词
Anti-inflammatory activity; Antiproliferative activity; Chromones; 1,2-Dihydropyridine-3-carboxylates; alpha-Glucosidase inhibitory activity; 3-Oxobutanoates; CELL-LINES; BENZOPHENONES; ANNULATION; INHIBITORS; CHROMONE;
D O I
10.1002/slct.201802809
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A one-pot, facile method has been established for the preparation of 1H-1,2,3-triazolyl 1,2-dihydropyridyl derivatives 6 a-y. The ring opening of the chromone and cyclo addition are the notable reactions to achieve the target compounds 6 a-y. All the compounds were screened for their antiproliferative, free radical scavenging (DPPH, ABTS(.+)), alpha-glucosidase inhibitory and anti-inflammatory activities. The bioactivity profile revealed that the compounds 6 x-y were shown potent antiproliferative activity against HeLa cell line, while compounds 6 e-h and 6 w identified as potent ABTS(+.) and 6 n identified as potent DPPH free radical scavenger. Compounds 6 h-i, 6 p-r, 6 u and 6 w denoted promising anti-inflammatory activity.
引用
收藏
页码:13729 / 13735
页数:7
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