发明名称 Substituted isoquinolin-1(2H)-ones, and methods of use thereof
摘要 Chemical entities that modulate PI3 kinase activity, pharmaceutical compositions containing the chemical entities, and methods of using these chemical entities for treating diseases and conditions associated with P13 kinase activity are described herein.
申请公布号 US8785456(B2) 申请公布日期 2014.07.22
申请号 US201213403394 申请日期 2012.02.23
申请人 Intellikine LLC 发明人 Ren Pingda;Liu Yi;Wilson Troy Edward;Li Liansheng;Chan Katrina;Rommel Christian
分类号 A61K31/52;C07D473/00 主分类号 A61K31/52
代理机构 Jones Day 代理人 Jones Day
主权项 1. A method of inhibiting a phosphatidyl inositol-3 kinase (PI3 kinase) in a subject, comprising administering to the subject an effective amount of a compound of Formula I-1:or a pharmaceutically acceptable salt thereof, wherein: B is a moiety of Formula II:wherein: Wc is aryl, heteroaryl, heterocycloalkyl, or cycloalkyl, and q is an integer of 0, 1, 2, 3, or 4; X is a bond or —(CH(R9))z—, and z is an integer of 1; Y is —N(R9)—; Wd is: R1 is hydrogen, alkyl, alkenyl, alkynyl, alkoxy, amido, alkoxycarbonyl, sulfonamido, halo, cyano, or nitro; R2 is alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, heteroarylalkyl, alkoxy, amino, halo, cyano, hydroxy or nitro; R3 is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, alkoxy, amido, amino, alkoxycarbonyl, sulfonamido, halo, cyano, hydroxy or nitro; and each instance of R9 is independently hydrogen, alkyl, or heterocycloalkyl.
地址 La Jolla CA US