The synthesis and anticonvulsant activity of some omega-phthalimido-N-phenylacetamide and propionamide derivatives
Articles > Article · 2004
Authors: Zeynep SOYER, FATMA SULTAN KILIÇ, KEVSER EROL, Mehmet Varol PABUÇÇUOĞLU
ARCHIV DER PHARMAZIE, Journal Indexed in SCI Expanded, International, 2004, vol 337, pp 105-111
Summary
In this study, by combining anilide and N',N'-phthaloylglycinamide pharmacophores which are known to produce potent anticonvulsant compounds, sixteen omega-phthalimido-N-phenylacetamide and propionamide derivatives bearing substituents at positions 2 or 2,6 on N-phenyl ring have been synthesized. The structural confirmation of the title compounds was achieved by interpretation of spectral and analytical data. The anticonvulsant activity of the title compounds was determined against maximal electroshock seizure at 100 mg/kg dose level in mice. The preliminary screening results indicated that omega-phthalimido-N-phenylacetamide and propionamide nuclei have pronounced anticonvulsant activity against maximal electroshock seizure.