Design of semicarbazones and their bio-isosteric analogues as potential anticonvulsants

Citation
Sn. Pandeya et al., Design of semicarbazones and their bio-isosteric analogues as potential anticonvulsants, PHARMAZIE, 56(2), 2001, pp. 121-124
Citations number
8
Categorie Soggetti
Pharmacology & Toxicology
Journal title
PHARMAZIE
ISSN journal
00317144 → ACNP
Volume
56
Issue
2
Year of publication
2001
Pages
121 - 124
Database
ISI
SICI code
0031-7144(200102)56:2<121:DOSATB>2.0.ZU;2-X
Abstract
A series of semicarbazones and hydrazones were prepared and evaluated for a nticonvulsant activity. Some compounds provided significant protection agai nst maximal electroshock (MES) and subcutaneous strychnine induced seizures (ScSty). Compound 2a emerged as the most active compound at a dose of 30 m g/kg in ScSty test. The compounds 1a. 1g and 2a-e showed significant potent iation of sedative and hypnotic activity of pentobarbitone sodium. Thus com pound 2a could serve as a prototype for future developments.