发明名称 Heterocyclic compounds useful for kinase inhibition
摘要 Provided herein are compounds useful for kinase inhibition.
申请公布号 US8957216(B2) 申请公布日期 2015.02.17
申请号 US201113636298 申请日期 2011.03.24
申请人 Amitech Therapeutic Solutions, Inc. 发明人 Arnold Lee Daniel;Murphy Eric A.
分类号 C07D401/12;C07D403/12;C07D401/14;C07D403/14;C07D409/14;C07D413/12;C07D487/04;C07D249/14;C07D413/14;C07D417/12;C07D471/04;C07D487/22 主分类号 C07D401/12
代理机构 Wilson Sonsini Goodrich & Rosati 代理人 Wilson Sonsini Goodrich & Rosati
主权项 1. A compound having the structure (I) or an N-oxide, N,N′-dioxide, N,N′,N″-trioxide, or a pharmaceutically acceptable saltthereof:wherein: Q is O; W is C6-C12 aryl; X is absent; Y is NH; Z1 and Z2 are N; Z3 is NRS, wherein R5 is hydrogen or C1-C6 alkyl; R1 is C3-C12 heteroaryl having 1-3 heteroatoms; optionally substituted with hydrogen, halogen, C1-C6 alkyl, —CF3, —OH, C1-C6 alkoxy, —NR10R11, and —SOmR12, wherein R10 and R11 are independently selected from a group consisting of hydrogen, C1-C6 alkyl, —SO2R12, —S(O)R12, and —COR12 and R12 is C1-C6 alkyl or C3-C12 heteroaryl having 1-3 heteroatoms and m is 0, 1 or 2; each R2 and R3 are independently selected from a group consisting of C1-C6 alkoxy, C1-C6 alkyl, C3-C12 cycloalkyl, and halogen; p is 1 or 2; or, optionally, R2 and R3 are joined to form a five to seven membered carbocycle; R4 is independently selected from a group consisting of hydrogen, halogen, C1-C6 alkyl; and n is 1 or 2.
地址 La Jolla CA US