发明名称 Methods of using pyruvate kinase activators
摘要 Described herein are methods for using compounds that activate pyruvate kinase.
申请公布号 US9388164(B2) 申请公布日期 2016.07.12
申请号 US201214115290 申请日期 2012.05.03
申请人 AGIOS PHARMACEUTICALS, INC 发明人 Su Shin-San M.
分类号 A61K31/535;C07D471/04;C07D401/12;A61K31/397;A61K31/4427;A61K31/4725;A01N1/02;C07D401/14 主分类号 A61K31/535
代理机构 Lando & Anastasi, LLP 代理人 Lando & Anastasi, LLP
主权项 1. A method for increasing the lifetime of red blood cells (RBCs) in need thereof comprising contacting blood with an effective amount of (1) a compound of formula I or a pharmaceutically acceptable salt thereof; (2) a composition comprising a compound of formula I or a salt thereof, and a carrier or (3) a pharmaceutically acceptable composition comprising a compound of formula I or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, wherein: A is aryl or heteroaryl, wherein the aryl or heteroaryl is optionally substituted, and the aryl or heteroaryl is optionally fused to an optionally substituted carbocyclyl or an optionally substituted heterocyclyl; X is selected from —NH—S(O)2—, —N(alkyl)-S(O)2—, —S(O)2—N(H)—, and —S(O)2—N(alkyl)-; R1a is selected from hydrogen, alkyl, and arylalkyl; and R1b is selected from OR3, N(alkyl)R3 and NHR3; or R1a is alken-1-yl and R1b is absent; each R2 is independently selected from halo, haloalkyl, alkyl, alkoxy and hydroxyl; R3 is selected from hydrogen, alkyl, optionally substituted aryl, optionally substituted heteroaryl, arylalkyl, C(O)Ra, and C(O)N(H)Ra, wherein Ra is selected from alkyl, alkenyl, aryl, heteroaryl, arylalkyl and heteroarylalkyl; and wherein any aryl or heteroaryl portion of Ra is optionally substituted; each R4 is independently selected from haloalkyl, alkyl, alkoxy and hydroxyl; n is 0, 1, or 2; and m is 0, 1, or 2.
地址 Cambridge MA US