| Literature DB >> 26230873 |
Luc J Farmer1, Mark W Ledeboer2, Thomas Hoock2, Michael J Arnost2, Randy S Bethiel2, Youssef L Bennani1, James J Black2, Christopher L Brummel2, Ananthsrinivas Chakilam2, Warren A Dorsch2, Bin Fan2, John E Cochran2, Summer Halas2, Edmund M Harrington2, James K Hogan2, David Howe2, Hui Huang2, Dylan H Jacobs2, Leena M Laitinen2, Shengkai Liao2, Sudipta Mahajan2, Valerie Marone2, Gabriel Martinez-Botella2, Pamela McCarthy2, David Messersmith2, Mark Namchuk2, Luke Oh2, Marina S Penney2, Albert C Pierce2, Scott A Raybuck2, Arthur Rugg2, Francesco G Salituro2, Kumkum Saxena2, Dean Shannon2, Dina Shlyakter2, Lora Swenson2, Shi-Kai Tian2, Christopher Town2, Jian Wang2, Tiansheng Wang2, M Woods Wannamaker2, Raymond J Winquist2, Harmon J Zuccola2.
Abstract
While several therapeutic options exist, the need for more effective, safe, and convenient treatment for a variety of autoimmune diseases persists. Targeting the Janus tyrosine kinases (JAKs), which play essential roles in cell signaling responses and can contribute to aberrant immune function associated with disease, has emerged as a novel and attractive approach for the development of new autoimmune disease therapies. We screened our compound library against JAK3, a key signaling kinase in immune cells, and identified multiple scaffolds showing good inhibitory activity for this kinase. A particular scaffold of interest, the 1H-pyrrolo[2,3-b]pyridine series (7-azaindoles), was selected for further optimization in part on the basis of binding affinity (Ki) as well as on the basis of cellular potency. Optimization of this chemical series led to the identification of VX-509 (decernotinib), a novel, potent, and selective JAK3 inhibitor, which demonstrates good efficacy in vivo in the rat host versus graft model (HvG). On the basis of these findings, it appears that VX-509 offers potential for the treatment of a variety of autoimmune diseases.Entities:
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Year: 2015 PMID: 26230873 DOI: 10.1021/acs.jmedchem.5b00301
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446