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Synthesis and analgesic-antiinflammatory activities of novel acylarylhydrazones with a 5-phenyl-4-R-3-pyrrolyl-acyl moiety
39
Citations
10
References
2001
Year
Medicinal ChemistryDerivative (Chemistry)Pharmacological StudyArylidene 5-Phenyl-4-r-pyrrole-3-carbohydrazides 1A-jMedicineNatural SciencesCompounds 1Pharmacological AgentOrganic ChemistryAnalgesic-antiinflammatory ActivitiesNew SeriesChemistry5-Phenyl-4-r-3-pyrrolyl-acyl MoietyNovel AcylarylhydrazonesPharmacologyPharmaceutical ChemistryDrug DiscoveryAnesthesiology
A new series of arylidene 5-phenyl-4-R-pyrrole-3-carbohydrazides 1a-j were prepared and evaluated for their analgesic-antiinflammatory activities. All synthesized compounds showed a significant analgesic action in mice after intraperitoneal administration at a dose of 100 microM/kg. Two of these, 1b, (4'-methylbenzylidene)-5-phenyl-1H-pyrrole-3-carbohydrazide, and 1d, (4'-chlorobenzylidene)-5-phenyl-1H-pyrrole-3-carbohydrazide, were found to be more potent as antinociceptive agents respect to dipyrone and indometacin, used as reference drugs. Among compounds 1, only 1b showed a moderate antiinflammatory effect in rats while 1d proved to be a potent non antiinflammatory analgesic.
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