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Design and comparative anticonvulsant activity assessment of CNS-active alkyl-carbamoyl imidazole derivatives
Institution:1. Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden;2. Institute of Pharmacology, Toxicology & Pharmacy, Ludwig-Maximilians-University, Munich, Germany;3. Department of Nuclear Medicine & PET Research, VU University Medical Center, Amsterdam, The Netherlands;4. Division of Pharmacology, LACDR, Leiden University, Leiden, The Netherlands;5. SEIN – Epilepsy Institutes of The Netherlands Foundation, Heemstede, The Netherlands;6. Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, London, United Kingdom
Abstract:A novel series of carbamoyl derivatives of alkylimidazole has been designed and their anticonvulsant activity was comparatively evaluated in the mice- and rats-maximal-electroshock (MES), subcutaneous-metrazol (scMet) seizure tests and the mice-6 Hz psychomotor (6 Hz) models. The ten new designed molecules contain in their chemical structure imidazole, alkyl side-chain and carbamate as three potential active moieties.In spite of the close structural features of the carbamoyl imidazole derivatives only compounds 7, 8, 13 and 16 were active at the MES test with ED50 values ranging from 12 to 20 mg/kg coupled with high protective index (PI = TD50/ED50) values of 4.1–7.3 after ip administration to rats. A similar phenomenon was observed in mice where compounds 7, 8, 9, 12 had MES-ED50 values of 14–26 mg/kg. Compounds 7 and 13 also demonstrated anticonvulsant activity in the 6 Hz model with ED50 values of 32 and 44 mg/kg, respectively. As the most active entities, compounds 7, 8 followed by 13 and 16, thus offer an optimal efficacy–safety profile and consequently, might be promising candidates for development as new antiepileptics.
Keywords:New antiepileptic drugs  Alkyl-carbamoyl imidazole derivatives  Anticonvulsant activity
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