| Literature DB >> 11806708 |
Salida Mirzoeva, Anu Sawkar, Magdalena Zasadzki, Ling Guo, Anastasia V Velentza, Vincent Dunlap, Jean-Jacques Bourguignon, Helena Ramstrom, Jacques Haiech, Linda J Van Eldik, D Martin Watterson.
Abstract
Excessive glial activation, with overproduction of cytokines and oxidative stress products, is detrimental and a hallmark of neurodegenerative disease pathology. Suppression of glial activation is a potential therapeutic approach, and protein kinases are targets of some antiinflammatory drugs. To address an unmet need for selective inhibitors of glial activation, we developed a novel 3-amino-6-phenylpyridazine derivative that selectively blocks increased IL-1 beta, iNOS, and NO production by activated glia, without inhibition of potentially beneficial glial functions.Entities:
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Year: 2002 PMID: 11806708 DOI: 10.1021/jm015573g
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446