Investigation of indole functionalized pyrazoles and oxadiazoles as anti-inflammatory agents: Synthesis, in-vivo, in-vitro and in-silico analysis

被引:29
|
作者
Kumar, Devendra [1 ]
Kumar, Ravi Ranjan [1 ]
Pathania, Shelly [1 ]
Singh, Pankaj Kumar [2 ]
Kalra, Sourav [3 ]
Kumar, Bhupinder [1 ]
机构
[1] ISF Coll Pharm, Dept Pharmaceut Chem, Ferozpur GT Rd MOGA, Ghal Kalan 142001, Punjab, India
[2] Univ Turku, Fac Med, Inst Biomed, Integrat Physiol & Pharmacol, FI-20520 Turku, Finland
[3] Natl Inst Pharmaceut Educ & Res, Dept Pharmaceut Technol Proc Chem, Sect 67, Mohali 160062, Punjab, India
关键词
Anti-inflammatory; Antioxidants; Indole derivatives; Oxadiazole derivatives; COX-2; inhibitors; BIOLOGICAL EVALUATION; COX-INHIBITION; DERIVATIVES; DOCKING; DRUGS; INFLAMMATION; RECEPTORS; IMMUNITY; RAT;
D O I
10.1016/j.bioorg.2021.105068
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There are several potential side and adverse effects are found to be associated with the anti-inflammatory drugs in clinical practice. The long-term use of these clinical agents highly unsafe. It encouraged the development of novel heterocyclic compounds with potential anti-inflammatory activity and low to no toxicity. In present investigation, a total of 12 indole functionalized pyrazole and oxadiazole derivatives were designed, synthesized and evaluated for the in-vivo anti-inflammatory and analgesic potential. These compounds displayed comparable anti-inflammatory and analgesic potential to the reference drugs. Finally, molecular docking analysis was performed considering different anti-inflammatory targets to determine the mechanistic target of the designed molecules. Detailed analysis suggested that the molecules inhibit COX-2, preferably over other anti-inflammatory targets. The results suggested that two compounds (15c and 15f) were found promising candidates for the development of novel anti-inflammatory agents.
引用
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页数:11
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