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Design and synthesis of potent pyridazine inhibitors of p38 MAP kinase. | LitMetric

AI Article Synopsis

  • A new type of pyridazine compound that targets p38 MAP kinase shows strong potential as an inhibitor.
  • These compounds effectively reduced cytokine release in cell-based tests and performed well in animal models, specifically for rheumatoid arthritis.
  • In studies, they significantly lowered TNF-alpha production in mice and showed good results in a rat model of collagen-induced arthritis.

Article Abstract

Novel potent trisubstituted pyridazine inhibitors of p38 MAP (mitogen activated protein) kinase are described that have activity in both cell-based assays of cytokine release and animal models of rheumatoid arthritis. They demonstrated potent inhibition of LPS-induced TNF-alpha production in mice and exhibited good efficacy in the rat collagen induced arthritis model.

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http://dx.doi.org/10.1016/j.bmcl.2005.02.010DOI Listing

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