发明名称 Substituted N-aryl pyridinones
摘要 Disclosed herein are substituted N-Aryl pyridinone fibrotic inhibitors and/or collagen infiltration modulators of Formula I, process of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.;
申请公布号 US9504677(B2) 申请公布日期 2016.11.29
申请号 US201514718993 申请日期 2015.05.21
申请人 Auspex Pharmaceuticals, Inc. 发明人 Gant Thomas G.;Sarshar Sepehr
分类号 A01N43/40;A61K31/44;C07D211/72;A61K31/4418;C07D213/64;A61K45/06;C07B59/00 主分类号 A01N43/40
代理机构 Baker & Hostetler LLP 代理人 Baker & Hostetler LLP
主权项 1. A method of treating or ameliorating one or more symptoms of a fibrotic-meditated disorder, a collagen-mediated disorder, or a fibrotic-mediated and collagen-mediated disorder in a patient in need of treatment, said method comprising administering to the patient a compound having the structure of Formula I: or a pharmaceutically acceptable salt, solvate, or prodrug thereof; wherein: R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, and R11 are independently selected from the group consisting of hydrogen and deuterium; at least one of R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, and R11 is deuterium; and at least one deuterium has a deuterium enrichment of no less than about 10%.
地址 LaJolla CA US