TRICYCLIC HETEROARYL COMPOUNDS USEFUL AS INHIBITORS OF JANUS KINASE
申请人:Bennani Yousseff
公开号:US20100081645A1
公开(公告)日:2010-04-01
The present invention relates to compounds useful as inhibitors of protein kinases, particularly of JAK family kinases. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders.
[EN] TRICYCLIC HETEROARYL COMPOUNDS USEFUL AS INHIBITORS OF JANUS KINASE<br/>[FR] COMPOSÉS HÉTÉROARYLE TRICYCLIQUES UTILES EN TANT QU'INHIBITEURS DE LA JANUS KINASE
申请人:VERTEX PHARMA
公开号:WO2008079521A2
公开(公告)日:2008-07-03
[EN] The present invention relates to compounds useful as inhibitors of protein kinases, particularly of JAK family kinases. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders. [FR] L'invention concerne des composés utiles en tant qu'inhibiteurs de protéine kinases, notamment des kinases de la famille JAK. L'invention concerne également des compositions pharmaceutiquement acceptables comprenant lesdits composés et des procédés d'utilisation des compositions dans le traitement de diverses pathologies, affections ou troubles.
Janus Kinase 2 Inhibitors. Synthesis and Characterization of a Novel Polycyclic Azaindole
作者:Tiansheng Wang、John P. Duffy、Jian Wang、Summer Halas、Francesco G. Salituro、Albert C. Pierce、Harmon J. Zuccola、James R. Black、James K. Hogan、Scott Jepson、Dina Shlyakter、Sudipta Mahajan、Yong Gu、Thomas Hoock、Mark Wood、Brinley F. Furey、J. Daniel Frantz、Lisa M. Dauffenbach、Ursula A. Germann、Bin Fan、Mark Namchuk、Youssef L. Bennani、Mark W. Ledeboer
DOI:10.1021/jm901383u
日期:2009.12.24
The Synthesis and characterization of a novel polycyclic azaindole based derivative is disclosed, and its binding to JAK2 is described. The compound is further evaluated for its ability to block the EPO/JAK2 signaling cascade in vitro and in vivo.