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J Med Chem ; 57(22): 9323-42, 2014 Nov 26.
Article in English | MEDLINE | ID: mdl-25369270

ABSTRACT

Janus kinases (JAK1, JAK2, JAK3, and TYK2) are involved in the signaling of multiple cytokines important in cellular function. Blockade of the JAK-STAT pathway with a small molecule has been shown to provide therapeutic immunomodulation. Having identified JAK1 as a possible new target for arthritis at Galapagos, the compound library was screened against JAK1, resulting in the identification of a triazolopyridine-based series of inhibitors represented by 3. Optimization within this chemical series led to identification of GLPG0634 (65, filgotinib), a selective JAK1 inhibitor currently in phase 2B development for RA and phase 2A development for Crohn's disease (CD).


Subject(s)
Chemistry, Pharmaceutical/methods , Janus Kinase 1/antagonists & inhibitors , Protein Kinase Inhibitors/chemistry , Pyridines/chemistry , Triazoles/chemistry , Adenosine Triphosphate/chemistry , Animals , Arthritis/drug therapy , Collagen/chemistry , Crohn Disease/drug therapy , Crystallography, X-Ray , Cytokines/metabolism , Dimerization , Disease Models, Animal , Drug Design , Drug Evaluation, Preclinical , Humans , Inhibitory Concentration 50 , Kinetics , Phosphorylation , Rats , Recombinant Proteins/chemistry , Structure-Activity Relationship
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