1159824-67-5Relevant articles and documents
SAR studies around a series of triazolopyridines as potent and selective PI3Kγ inhibitors
Bell, Kathryn,Sunose, Mihiro,Ellard, Katie,Cansfield, Andrew,Taylor, Jess,Miller, Warren,Ramsden, Nigel,Bergamini, Giovanna,Neubauer, Gitte
scheme or table, p. 5257 - 5263 (2012/09/07)
Herein we describe the SAR of a novel series of 6-aryl-2-amino- triazolopyridines as potent and selective PI3Kγ inhibitors. The 6-aryl-triazolopyridine core was identified by chemoproteomic screening of a kinase focused library. Rapid chemical expansion a
UREA TRIAZOLOLO [1, 5-A] PYRIDINE DERIVATIVES AS PI3K INHIBITORS
-
Page/Page column 50, (2010/09/03)
The invention relates to compounds of formula (I) wherein X1,R and R1 to R4 have the meaning as cited in the description and the claims. Said compounds are useful as protein kinase inhibitors, especially inhibitors of PI3K, for the treatment or prophylaxis of immunological, inflammatory, autoimmune, or allergic disorders. The invention also relates to pharmaceutical compositions including said compounds, the preparation of such compounds as well as the production of and use as medicaments.
AMINO TRIAZOLES AS PI3K INHIBITORS
-
Page/Page column 84-85, (2009/07/03)
The invention relates to compounds of formula (I) Said compounds are useful as protein kinase inhibitors, especially inhibitors of P13K, for the treatment or prophylaxis of immunological, inflammatory, autoimmune, or allergic disorders. The invention also relates to pharmaceutical compositions including said compounds, the preparation of such compounds as well as the production of and use as medicaments.