Ozer, Erdem KamilGunduz, Miyase GozdeEl-Khouly, AhmedSara, YildirimSimsek, RahimeIskit, Alper BektasSafak, Cihat2020-03-262020-03-2620180250-46851303-829Xhttps://dx.doi.org/10.1515/tjb-2016-0247https://hdl.handle.net/20.500.12395/36973Objective: The aim of this study was to synthesize ten 1,4-dihydropyridine (DHP) derivatives in which substituted cyclohexane rings were fused to the DHP ring and to determine how different ester groups and the benzoyl substituent introduced in 4-phenyl ring affected their calcium channel blocking activity. Methods: A microwave-assisted one-pot method was applied for the synthesis of compound 1-5 according to a modified Hantzsch reaction. The benzoyl moiety was introduced in the 4-phenyl ring of these dihydropyridines by refluxing with benzoyl chloride in acetone in the presence of anhydrous potassium carbonate. Synthesized products were characterized by elemental analysis, IR, H-1-NMR and C-13-NMR spectroscopy. The inhibitory actions of compounds 1-10 on calcium channel blocking activity were tested on isolated rat aorta preparations. Results: The obtained pharmacological results showed that although all compounds are potent relaxing agents on isolated rat aorta smooth muscle, introduction of a benzoyloxy substitiuent on the phenyl ring (compound 6-10) decreased the relaxant effect of these compunds. Conclusion: The reported 1,4-DHP derivatives have calcium channel blocking activity on rat aorta smooth muscle.en10.1515/tjb-2016-0247info:eu-repo/semantics/closedAccess1,4-DihydropyridineCalcium channelHexahydroquinolineIsolated aortic ringsRelaxant effectsArticle436578586Q4WOS:000450015000002Q4