发明名称 Thromboxane A2 (TP) receptor antagonists
摘要 The present invention relates to novel TP receptor antagonists, which optionally cross the blood-brain barrier of a mammal. The invention also provides methods for treating a disorder related to activation of TP receptor utilizing the compounds of the invention.
申请公布号 US8927586(B2) 申请公布日期 2015.01.06
申请号 US201313780458 申请日期 2013.02.28
申请人 The Trustees of the University of Pennsylvania 发明人 Trojanowski John Q.;Lee Virginia M. Y.;Brunden Kurt R.;Smith Amos B.;Huym Donna M.;Ballatore Carlo;Hogan Anne-Marie;Piscitelli Francesco;Shimpei Sugiyama;Wang Xiaozhao
分类号 C07C311/20;C07D317/28;A61K31/18;A61K31/196;A61K31/216;A61K31/357;A61K31/41;A61K31/4174;A61K31/421;A61K31/426;A61K45/06;C07D233/64;C07D257/04;C07D263/32;C07D277/28 主分类号 C07C311/20
代理机构 Saul Ewing, LLP 代理人 Saul Ewing, LLP ;Doyle Kathryn
主权项 1. A composition comprising a compound of Formula (I), or a salt or solvate thereof:wherein: R1 is selected from the group consisting of the bond between carbons 1 and 2 is either a single bond (C1-C2) or a double bond (C1═C2); R2 is selected from the group consisting of F, Cl, Br, I, and CF3; R3 is selected from the group consisting of NR4, S, and O; R4 is selected from the group consisting of H, —(C1-C6 alkyl), —(C1-C6 fluoroalkyl), —(C1-C6 heteroalkyl), —(C1-C3 alkyl)-(C3-C6 cycloalkyl), —(C1-C3 alkyl)-aryl, —(C1-C3 alkyl)-heteroaryl, —C(═O)R5, —CO2R5, and —CH(R)2; and, each occurrence of R5 is independently selected from the group consisting of H, —(C1-C6 alkyl), —(C1-C6 heteroalkyl), and —(C1-C3 alkyl)-(C3-C6 cycloalkyl), wherein the alkyl, heteroalkyl, or cycloalkyl group is optionally substituted.
地址 Philadelphia PA US