Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/56389
Title: Synthesis and anticonvulsant activity of some 1,4-dihydropyridine derivatives
Authors: Begum, Safia
Sirisha, Kalam
Keywords: 1,4-Dihydropyridine;Hantzsch method;Pentylenetetrazole;Anticonvulsant;Synthesis
Issue Date: Mar-2021
Publisher: NISCAIR-CSIR, India
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.
Page(s): 433-438
URI: http://nopr.niscair.res.in/handle/123456789/56389
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.60B(03) [March 2021]

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