| Literature DB >> 24205976 |
David F McComsey1, Virginia L Smith-Swintosky, Michael H Parker, Douglas E Brenneman, Ewa Malatynska, H Steve White, Brian D Klein, Karen S Wilcox, Michael E Milewski, Mark Herb, Michael F A Finley, Yi Liu, Mary Lou Lubin, Ning Qin, Allen B Reitz, Bruce E Maryanoff.
Abstract
Broad-spectrum anticonvulsants are of considerable interest as antiepileptic drugs, especially because of their potential for treating refractory patients. Such "neurostabilizers" have also been used to treat other neurological disorders, including migraine, bipolar disorder, and neuropathic pain. We synthesized a series of sulfamide derivatives (4-9, 10a-i, 11a, 11b, 12) and evaluated their anticonvulsant activity. Thus, we identified promising sulfamide 4 (JNJ-26489112) and explored its pharmacological properties. Compound 4 exhibited excellent anticonvulsant activity in rodents against audiogenic, electrically induced, and chemically induced seizures. Mechanistically, 4 inhibited voltage-gated Na(+) channels and N-type Ca(2+) channels and was effective as a K(+) channel opener. The anticonvulsant profile of 4 suggests that it may be useful for treating multiple forms of epilepsy (generalized tonic-clonic, complex partial, absence seizures), including refractory (or pharmacoresistant) epilepsy, at dose levels that confer a good safety margin. On the basis of its pharmacology and other favorable characteristics, 4 was advanced into human clinical studies.Entities:
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Year: 2013 PMID: 24205976 PMCID: PMC4004761 DOI: 10.1021/jm400894u
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446