Synthesis and biological evaluation of pyrazolone analogues as potential anti-inflammatory agents targeting cyclooxygenases and 5-lipoxygenase

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dc.contributor.author Mohamed, K.O
dc.contributor.author Elsahar, A.E
dc.contributor.author Faggal, S.I
dc.contributor.author Kamal, A.M
dc.contributor.author Shabaan, M.A.
dc.date.accessioned 2020-02-14T14:16:15Z
dc.date.available 2020-02-14T14:16:15Z
dc.date.issued 2020
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Cited 19 times. www.interscience.wiley.com doi: 10.1002/ardp.201700026 en_US
dc.identifier.issn 3656233
dc.identifier.other https://doi.org/10.1002/ardp.201900308
dc.identifier.uri https://www.ncbi.nlm.nih.gov/pubmed/32031284
dc.description scopus en_US
dc.description.abstract New pyrazolone derivatives structurally related to celecoxib and FPL 62064 were synthesized and biologically evaluated for their inhibitory activity against cyclooxygenases (COXs) and 5-lipoxygenase (5-LOX) and their selectivity indices were calculated. The results showed that compounds 3f, 3h, 3l, and 3p have an excellent COX-2 selectivity index. Moreover, they showed potent 5-LOX inhibitory activity relative to celecoxib and zileuton, as positive controls. These promising candidates were further investigated for anti-inflammatory activity using the carrageenan-induced rat paw edema method and ulcerogenic liability. The results showed no ulceration, which implies their gastric safety profile. Moreover, these compounds were evaluated for prostaglandin (PGE2) production in rat serum. Molecular docking in the COX-2 and 5-LOX active sites was performed to rationalize their anti-inflammatory activities. Strong binding interactions and effective docking scores were identified. The results indicated that these derivatives are good leads for dual-acting COX-2/5-LOX inhibitors to be used as potent and safe anti-inflammatory agents. © 2020 Deutsche Pharmazeutische Gesellschaft en_US
dc.description.uri https://www.scimagojr.com/journalsearch.php?q=19956&tip=sid&clean=0
dc.language.iso en en_US
dc.publisher Wiley-VCH Verlag en_US
dc.relation.ispartofseries Archiv der Pharmazie;2020, Article number e1900308
dc.subject pyrazolone en_US
dc.subject PGE2 en_US
dc.subject COX-2 inhibitors en_US
dc.subject anti-inflammatory en_US
dc.subject 5-LOX en_US
dc.title Synthesis and biological evaluation of pyrazolone analogues as potential anti-inflammatory agents targeting cyclooxygenases and 5-lipoxygenase en_US
dc.type Article en_US
dc.identifier.doi https://doi.org/10.1002/ardp.201900308
dc.Affiliation October University for modern sciences and Arts (MSA)


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