Abstract
A novel series of 1-(4-phenoxyphenyl)-3-[5-(substituted aryl)-1,3,4-oxadiazol-2-yl]propan-1-one was synthesized by reaction of 3-(4-phenoxybenzoyl) propionic acid with several aryl acid hydrazides in phosphorus oxychloride. The structures of the compounds were supported by IR, 1H- and 13C-NMR, MS data and elemental analysis results. These compounds were tested for their anti-inflammatory, analgesic, ulcerogenic and lipid peroxidation actions. A few compounds were found to have very good anti-inflammatory activity in the carrageenan-induced rat paw edema test, while a fair number of the compounds showed significant analgesic activity in the acetic acid-induced writhing test. These new compounds showed very low ulcerogenic action with reduced malondialdehyde content (MDA), which is one of the by-products of lipid peroxidation.
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Husain, A., Ahmad, F. J., Ajmal, M., & Ahuja, P. (2008). Synthesis of 1-(4-phenoxyphenyl)-3-[5-(substituted aryl)-1,3,4-oxadiazol-2- yl]propan-1-ones as safer anti-inflammatory and analgesic agents. Journal of the Serbian Chemical Society, 73(8–9), 781–791. https://doi.org/10.2298/JSC0809781H
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