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ScientificWorldJournal ; 2012: 925925, 2012.
Article in English | MEDLINE | ID: mdl-23304092

ABSTRACT

Four new 1,2,3-triazole phthalimide derivatives with a potent anti-inflammatory activity have been synthesized in the good yields by the 1,3-dipolar cycloaddition reaction from N-(azido-alkyl)phthalimides and terminal alkynes. The anti-inflammatory activity was determined by injecting carrageenan through the plantar tissue of the right hind paw of Swiss white mice to produce inflammation. All the compounds 3a-c and 5a-c exhibited an important anti-inflammatory activity; the best activity was found for the compounds 3b and 5c, which showed to be able to decrease by 69% and 56.2% carrageenan-induced edema in mice. These compounds may also offer a future promise as a new anti-inflammatory agent.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/chemical synthesis , Chemistry, Pharmaceutical/methods , Phthalimides/chemical synthesis , Triazoles/chemical synthesis , Animals , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Carrageenan/toxicity , Chemistry, Pharmaceutical/trends , Dose-Response Relationship, Drug , Edema/chemically induced , Edema/drug therapy , Inflammation/chemically induced , Inflammation/drug therapy , Mice , Phthalimides/therapeutic use , Triazoles/therapeutic use
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