Synthesis and Anticonvulsant Activity of Various Mannich and Schiff Bases of 1,5-BenzodiazepinesReportar como inadecuado

Synthesis and Anticonvulsant Activity of Various Mannich and Schiff Bases of 1,5-Benzodiazepines - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

International Journal of Medicinal ChemistryVolume 2012 2012, Article ID 237965, 10 pages

Research ArticleDepartment of Pharmaceutical Sciences, Saroj Institute of Technology and Management, Sultanpur Road, Lucknow 226002, India

Received 6 May 2012; Revised 6 September 2012; Accepted 28 September 2012

Academic Editor: Jochen Lehmann

Copyright © 2012 Surendra N. Pandeya and Neha Rajput. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Benzodiazepines have a various behavioral effects in addition to their anxiolytic action. There is every reason to believe that the BZ-GABA receptor complex is involved in these effects, since GABAmimetic manipulations modify the effect of BZ in tests of convulsive activity, motor function, and appetitive behavior. 1,5-Benzodiazepines are biologically important molecules and are extensively used clinically as analgesic, hypnotic, sedative, and antidepressive agents. Hence, 1,5-Benzodiazepines were synthesized by condensation of o-phenylenediamine and ketones, for example, cyclohexanone and acetone in presence of sulfated zirconia catalyst. Mannich bases were synthesized with acetophenone, p-nitroacetophenone, p-chloroacetophenone, and formaldehyde. Schiff bases were synthesized using Mannich base of 1,5-benzodiazepines with p-chloroaniline and p-chlorophenylsemicarbazide in the presence of glacial acetic acid. All the synthesized compounds were characterized by

H NMR and IR spectral analyses. All the synthesized derivatives were evaluated at the dose of 30 mg-kg b.w for anticonvulsant activity by isoniazid induced convulsion model, and the compounds NBZD-3 and NBZD-8 were found to be the most active among all compounds. Among all the synthesized derivatives, compounds NBZD-13 and NBZD-17 were found to be the most active among all compounds using thiosemicarbazide induced model. Although NBZD-8, NBZD-10, and NBZD-18 are the compounds which had shown good anticonvulsant activity and have an advantage over that, they were not sedative.

Autor: Surendra N. Pandeya and Neha Rajput



Documentos relacionados