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Conjugation of some NSAIDs with 5-phenyl-2-aminothiazole for reduced ulcerogenicity

dc.contributor.authorVerma A.; Das N.; Dhanawat M.; Shrivastava S.K.
dc.date.accessioned2025-05-24T09:57:43Z
dc.description.abstractAnalgesic drugs containing free acidic group were reacted with N, N' carbonyldiimidazole to prepare the acylimidazole derivatives. They were further reacted with 5-phenyl-2-amino thiazole nucleus to obtain the corresponding amides. All the compounds were found to retain analgesic-antiinflammatory activities with much lesser NSAID-induced GI complications when compared with the standard.
dc.identifier.doiDOI not available
dc.identifier.urihttp://172.23.0.11:4000/handle/123456789/22450
dc.relation.ispartofseriesThai Journal of Pharmaceutical Sciences
dc.titleConjugation of some NSAIDs with 5-phenyl-2-aminothiazole for reduced ulcerogenicity

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