David P. Cardin - Wilmington MA, US Paul Greenspan - Acton MA, US Stepan Vyskocil - Arlington MA, US Jeffrey Gaulin - Rockingham NH, US Tianlin Xu - Shrewsbury MA, US Christelle C. Renou - Stoneham MA, US
David P. Cardin - Wilmington MA, US Jeffrey Gaulin - Rockingham NH, US Paul Greenspan - Acton MA, US Christelle C. Renou - Stoneham MA, US Stepan Vyskocil - Arlington MA, US Tianlin Xu - Shrewsbury MA, US
- Cambridge MA, US David P. Cardin - Wilmington MA, US Takaharu Hirayama - Kanagawa, JP Masaaki Hirose - Tokyo, JP Yongbo Hu - Winchester MA, US Hiroyuki Kakei - Kanagawa, JP Hong Myung Lee - Cambridge MA, US Takashi Motoyaji - Kanagawa, JP Noriyuki Nii - Kanagawa, JP Zhan Shi - Concord MA, US Stepan Vyskocil - Arlington MA, US Hiroyuki Watanabe - Hyogo, JP
This invention provides compounds of formula I and subsets thereof: wherein T, J, R, R, R, o, R, and Rand subsets thereof are as described in the specification. The compounds are inhibitors of NAMPT and are thus useful for treating cancer, inflammatory conditions, or T-cell mediated autoimmune disease.
Indole-Substituted Pyrrolopyrimidinyl Inhibitors Of Uba6
- Cambridge MA, US David P. Cardin - Wilmington MA, US Alexandra E. Gould - Cambridge MA, US Paul D. Greenspan - Acton MA, US Sean J. Harrison - Belmont MA, US
International Classification:
C07D 487/04
Abstract:
Disclosed are chemical entities that inhibit Uba6, each of which is a compound of Formula /: Formula (I) or a pharmaceutically acceptable salt thereof, wherein R*is —H or —CH; and Y is Formula (II) or Formula (III), wherein Ris —H, —CHor Calkyloxycarbonyl; and R, Rand Rare defined herein; pharmaceutical compositions comprising the chemical entities; and methods of using the chemical entities. These chemical entities are useful for treating disorders, particularly cell proliferation disorders, including cancers.