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J Med Chem ; 45(3): 563-6, 2002 Jan 31.
Article in English | MEDLINE | ID: mdl-11806708

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.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/chemical synthesis , Central Nervous System Agents/chemical synthesis , Pyridazines/chemical synthesis , Animals , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Astrocytes/metabolism , Calcium-Calmodulin-Dependent Protein Kinase Type 2 , Calcium-Calmodulin-Dependent Protein Kinases/antagonists & inhibitors , Cells, Cultured , Central Nervous System Agents/chemistry , Central Nervous System Agents/pharmacology , Drug Evaluation, Preclinical , Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/chemistry , Enzyme Inhibitors/pharmacology , Interleukin-1/antagonists & inhibitors , Microglia/drug effects , Nitric Oxide/antagonists & inhibitors , Nitric Oxide/metabolism , Nitric Oxide Synthase/antagonists & inhibitors , Nitric Oxide Synthase Type II , Pyridazines/chemistry , Pyridazines/pharmacology , Rats , Structure-Activity Relationship
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