发明名称 Proteostasis regulators
摘要 The present invention is directed to compounds having the Formulae (Ia-Ie), (II), (IIIa-IIId), (IVa-IVc), (Va-Vb), (VIa-VIe), (VII), (VIIIa-VIIIc), and (IX), pharmaceutically acceptable salts, prodrugs and solvates thereof, compositions of any of thereof and methods for the treatment of a condition associated with a dysfunction in proteostasis comprising an effective amount of these compounds.
申请公布号 US9556166(B2) 申请公布日期 2017.01.31
申请号 US201213468757 申请日期 2012.05.10
申请人 Proteostasis Therapeutics, Inc. 发明人 Foley Megan;Tait Bradley;Cullen Matthew
分类号 C07D401/06;C07D403/06;C07D405/06;C07D471/04;C07D207/333;C07D207/337;C07D231/12;C07D249/06;C07D263/32;C07D275/02;C07D295/185;C07D333/20 主分类号 C07D401/06
代理机构 Elmore Patent Law Group, P.C. 代理人 Elmore Patent Law Group, P.C. ;Hoda Mahreen Chaudhry;Elmore, Esq. Carolyn S.
主权项 1. A compound having the Formula (II): or a pharmaceutically acceptable salt, or solvate thereof, wherein: D is optionally substituted phenyl; Q is C(Rd); each Ri is independently selected from the group consisting of hydrogen and optionally substituted C1-C10 alkyl; R5 and R6 are each independently selected from the group consisting of hydrogen and optionally substituted C1-C10 alkyl; Z1 is NRcRc; each Rc is independently selected from the group consisting of hydrogen and optionally substituted C1-C10 alkyl; or alternatively, the two Rc groups are taken together with the nitrogen atom to which they are attached to form an optionally substituted 3- to 8-membered heterocyclic; and Rd is optionally substituted C1-C10 alkyl.
地址 Cambridge MA US