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 |