发明名称 BROMODOMAIN INHIBITORS FOR TREATING DISEASE
摘要 Disclosed herein are compounds and compositions useful in the treatment of bromodomain-containing protein-mediated diseases, such as cancer, having the structure of Formula I:;;Methods of inhibiting activity of a bromodomain-containing protein in a human or animal subject are also provided.
申请公布号 US2016060260(A1) 申请公布日期 2016.03.03
申请号 US201514838570 申请日期 2015.08.28
申请人 Board of Regents, The University of Texas System 发明人 Palmer Wylie;Jones Philip;Liu Gang;Petrocchi Alessia;Reyna Naphtali;Subrumanian Govindan;Theroff Jay;Yau Anne
分类号 C07D471/04;A61K31/498;A61K31/437;A61K31/454;A61K31/4439;A61K31/4184;C07D401/14;C07D403/12;C07D235/26;A61N5/10;C07D401/12;C07D405/12;C07D405/14;A61K45/06;A61B18/02;A61N7/00;A61K31/5377 主分类号 C07D471/04
代理机构 代理人
主权项 1. A compound of structural Formula I or a salt thereof, wherein: m is chosen from the integers 0, 1, 2, and 3; X is chosen from alkyl, aryl, cycloalkyl, heteroaryl, heteroarylalkyl, heterocycloalkyl, and heterocycloalkylalkyl; each R1 is independently chosen from alkenyl, alkyl, H, and haloalkyl; each R2 is independently chosen from alkenyl, alkoxy, alkyl, aryl, arylalkyl, cyano, cycloalkyl, H, halo, haloalkoxy, heteroaryl, heteroarylalkyl, heterocycloalkyl, hydroxyl, N(R3)2, C(O)OH, N(R3)C(O)C(R3)3, N(R3)C(O)OC(R3)3, C(O)OC(R3)3, and C(O)N(R3)2, wherein two R2 groups together with the atoms to which they are attached optionally form an aryl, cycloalkyl, heteroaryl, or heterocycloalkyl ring, which may be optionally substituted with between 0 and 3 R3 groups; each R3 is independently chosen from alkenyl, alkoxy, alkyl, aminoalkyl, aryl, arylalkyl, cyano, cycloalkyl, cycloalkylalkyl, cycloalkylalkoxy, H, halo, haloalkyl, heteroaryl, heteroarylalkyl, heterocycloalkyl, heterocycloalkylalkyl, and hydroxyl; and G is phenyl, which may be optionally substituted.
地址 Austin TX US