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|Title:||Synthesis and anticonvulsant activity of some 1,4-dihydropyridine derivatives|
|Abstract:||A series of asymmetrical 4-alkyl/aryl-2,6-dimethyl-3-N-(aryl/heteroaryl)-carbamoyl-5-ethoxycarbonyl-1, 4-dihydropyridines 3a-d and symmetrical 4-alkyl/aryl-2,6-dimethyl-3,5-bis-(ethoxycarbonyl)-1,4-dihydropyridines 4a and 4b have been prepared by the condensation of various benzaldehydes, ethylacetoacetate, 2-aminopyridine or p-toludine in ethanol (Hantzch method). The structures of all the synthesized 1,4-dihydropyridine derivatives have been confirmed by spectral data (IR, 1H NMR) and elemental analysis. Compounds 3a-c, 4a and 4b (10 mg/kg) have been evaluated for their anticonvulsant effect against pentylenetetrazole- induced convulsions with phenytoin (4 mg/kg) as the standard. The anticonvulsant potential of the newly synthesized compounds have been assessed on the basis of increase in latency (onset time) to induce convulsions; decrease in number of convulsions and increase in latency of death compared to control and standard.|
|Appears in Collections:||IJC-B Vol.60B(03) [March 2021]|
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|IJCB 60B(3) 433-438.pdf||Main Article||193.81 kB||Adobe PDF||View/Open|
|IJCB 60B(3) 433-438_Suppl Data.pdf||Supplementary Data||51.96 kB||Adobe PDF||View/Open|
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