发明名称 SUBSTITUTED PYRIDINES AS P2X3 AND P2X2/3 ANTAGONISTS
摘要 Methods of treating diseases associated with P2X3 and/or a P2X2/ with compounds;;formula I: or a pharmaceutically acceptable salt thereof, wherein, X, Y, R1, R2, R3, R4, R5, R6 and R7 are as defined herein.
申请公布号 US2017056398(A1) 申请公布日期 2017.03.02
申请号 US201615347629 申请日期 2016.11.09
申请人 Roche Palo Alto LLC 发明人 Chen Li;Dillon Michael Patrick;Feng Lichun;Yang Minmin
分类号 A61K31/497 主分类号 A61K31/497
代理机构 代理人
主权项 1. A method for modulating P2X3 and R2X2/3 receptor activity in a subject comprising administering to a subject in need thereof an therapeutically effective amount of a compound of formula I, or a pharmaceutically acceptable salt thereof, wherein: R1 is C1-6alkyl or halo; R2 is C3-6cycloalkyl, C1-6alkoxy-C1-6alkyl, hydroxy-C1-6alkyl, or heteroaryl-C1-6alkyl; R3 is hydrogen, halo, C1-6alkyl, or C1-6alkoxy-carbonyl; R4 is hydrogen, halo, C1-6alkyl; or, R3 and R4 together with the atoms to which they are attached may form a fused 6-membered aromatic ring that optionally includes one or two nitrogens; or, R3 and R4 together with the atom to which they are attached may form C3-6cycloalkyl; R5, R6 and R7 each independently is fluoro or hydrogen. X is CRa− wherein Ra is C1-6alkyl or halo; and, Y is —O—, —CHRb—, or —NRc—, wherein Rb and Rc each independently is hydrogen or C1-6alkyl;with the proviso that when Y is CH2, R2 is C3-6cycloalkyl, C1-6alkoxy-C1-6alkyl, or hydroxy-C1-6alkyl.
地址 South San Francisco CA US