Eleven antipyrine/pyridazinone hybrids were synthesized and evaluated for their in vivo analgesic and anti-inflammatory activities by p-benzoquinone- induced writhing test and carrageenan-induced paw edema model, respectively. The test results indicated that compounds 6a, 6c, and 6d were equally or more potent analgesic and anti-inflammatory agents than aspirin and indomethacin, respectively. Side effects of the compounds were examined on gastric mucosa. Most of the compounds were found to be non-ulcerogenic under test conditions. © TÜBİTAK, 2012.
CITATION STYLE
Baytaş, S., Inceler, N., Mavaneh, K. F., Uludaǧ, M. O., Abacioǧlu, N., & Gökçe, M. (2012). Synthesis of antipyrine/pyridazinone hybrids and investigation of their in vivo analgesic and anti-inflammatory activities. Turkish Journal of Chemistry, 36(5), 734–748. https://doi.org/10.3906/kim-1111-29
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