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

Article Details

Citation

Tamayo N, Liao L, Goldberg M, Powers D, Tudor YY, Yu V, Wong LM, Henkle B, Middleton S, Syed R, Harvey T, Jang G, Hungate R, Dominguez C

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

Bioorg Med Chem Lett. 2005 May 2;15(9):2409-13.

PubMed ID
15837335 [ View in PubMed
]
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.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Mitogen-activated protein kinase 14Q16539Details