| Literature DB >> 27933950 |
Romain Siegrist1, Davide Pozzi1, Gaël Jacob1, Caterina Torrisi1, Kilian Colas1, Bertrand Braibant1, Jacques Mawet1, Thomas Pfeifer1, Ruben de Kanter1, Catherine Roch1, Melanie Kessler1, Richard Moon, Olivier Corminboeuf1, Olivier Bezençon1.
Abstract
Despite the availability of numerous antiepileptic drugs, 20-30% of epileptic patients are pharmacoresistant with seizures not appropriately controlled. Consequently, new strategies to address this unmet medical need are required. T-type calcium channels play a key role in neuronal excitability and burst firing, and selective triple T-type calcium channel blockers could offer a new way to treat various CNS disorders, in particular epilepsy. Herein we describe the identification of new 1,4-benzodiazepines as brain penetrant and selective triple T-type calcium channel blockers. From racemic hit 4, optimization work led to the preparation of pyridodiazepine 31c with improved physicochemical properties, solubility, and metabolic stability. The racemic mixture was separated by chiral preparative HPLC, and the resulting lead compound (3R,5S)-31c showed promising efficacy in the WAG/Rij-rat model of generalized nonconvulsive absence-like epilepsy.Entities:
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Year: 2016 PMID: 27933950 DOI: 10.1021/acs.jmedchem.6b01356
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446