Anticonvulsant Activity and Selective Inhibition of NAD-Dependent Oxidations by 1,2,4-Trisubstituted-5-Imidazolones

Abstract

Nine 1-(3,4-dimethoxyphenylethyl)-2-methyl-4-(substituted benzylidene)-5-imidazolones were synthesized, characterized by their sharp melting points, elemental analyses and infrared spectra and evaluated for anticonvulsant activity. All l,2,4-trisubstituted-5-imidazolones at a dose of 100 mg/kg i.p. possessed anticonvulsant activity and the degree of protection observed against pentylenetetrazol-induced convulsions in mice ranged from 20 to 60%. These 1,2,4-trisubstituted-5-imidazolones selectively inhibited in vitro oxidation of the nicotinamide adenine dinucleotide (NAD)-dependent oxidation of pyruvate, α-ketoglutarate and NADH by rat brain homogenates while the NAD-independent oxidation of succinate remained unaltered. The anticonvulsant activity possessed by 1,2,4-trisubstituted-5-imidazolones was unrelated with their ability to selectively inhibit respiratory activity of rat brain homogenates.

The Meta-Green Fluorescent Protein Chromophore

“…The corresponding methyl ether m - MBDI was also prepared. It is noteworthy that, despite the previously unknown nature of m - HBDI itself, several 2-methyl-substituted derivatives exhibiting various biological activities have been synthesized 2 Left column: absorption spectra of p - HBDI (top) and m - HBDI (bottom) in methanol/water (MW) 1/1 vol.…”

Recent Developments and Biological Activities of 5-Oxo-Imidazolones Derivatives: A Review

“…and reported their anticonvulsant activity. These results showed that introduction of a substituent in the phenyl nucleus of benzylidene moiety increased the anticonvulsant activity [61].…”