Synthesis, analgesic, anti-inflammatory, ulcerogenic evaluation, and docking study of (benzoylphenoxy)-N-{5-2-methylphenyl-6-chlorobenzoxazole]} acetamides as COX/5-LOX inhibitor

Khadri, M. J. Nagesh and Khamees, Hussien Ahmed and Kouser, Salma and Zabiulla and Shaukath Ara Khanum (2023) Synthesis, analgesic, anti-inflammatory, ulcerogenic evaluation, and docking study of (benzoylphenoxy)-N-{5-2-methylphenyl-6-chlorobenzoxazole]} acetamides as COX/5-LOX inhibitor. Journal of Molecular Structure, 1272. ISSN 1872-8014

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Official URL: https://doi.org/10.1016/j.molstruc.2022.134240

Abstract

The COX and 5-LOX inhibitors with analgesic and anti-inflammatory effectiveness and very less gastrointestinal toxicity have been recognized as constructive and sustainable agents for inflammatory treatment. In this approach, a series of titled compounds (10a-j) were developed, synthesized, and evaluated in terms of in-vitro COX and LOX enzyme inhibition followed by analgesic, anti-inflammatory, and the ulcerogenic activity. The anti-inflammatory evaluation was conducted on those compounds 10a-c, 10e, and 10g-10i that displayed potential analgesic activity and later, validated for the ulcerogenic effect of potent anti-inflammatory compounds. The compound 10b with ortho substitution of methyl and para substitution of chloro groups on the phenyl ring and meta substitution of chloro group on benzoyl ring of benzophenone appended to benzoxazole was observed to have good inhibitory potency. Furthermore, Autodock tools docking software was used to carry out the in silico studies. (c) 2022ElsevierB.V. Allrights reserved.

Item Type: Article
Uncontrolled Keywords: Benzoxazole; Analgesic; Anti-inflammatory; COX-1/COX-2 inhibition; 5-LOX inhibition; Ulcerogenic; Docking studies
Subjects: C Chemical Science > Chemistry
Divisions: Yuvaraj college > Chemistry
Depositing User: C Swapna Library Assistant
Date Deposited: 15 Jul 2023 10:04
Last Modified: 15 Jul 2023 10:04
URI: http://eprints.uni-mysore.ac.in/id/eprint/17632

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