发明名称 Pyrido[2,3-b]pyrazine compounds useful as IP receptor agonist
摘要 The present invention provides heterocyclic derivatives which activate the IP receptor. Activating the IP receptor signaling pathway is useful to treat many forms of PAH, pulmonary fibrosis and exert beneficial effects in fibrotic conditions of various organs in animal models and in patients. Pharmaceutical compositions comprising such derivatives are also encompassed. Examples of compounds of the invention include the compounds according to Formula Ia, or a pharmaceutically acceptable salt thereof, and the compounds of the examples.;
申请公布号 US8754085(B2) 申请公布日期 2014.06.17
申请号 US201113388819 申请日期 2011.07.14
申请人 Novartis AG 发明人 Charlton Steven John;Leblanc Catherine;McKeown Stephen Carl
分类号 A61K31/495 主分类号 A61K31/495
代理机构 代理人
主权项 1. A compound, or a pharmaceutically acceptable salt thereof, selected from the group consisting of: 7-(2,3-diphenyl-7,8-dihydropyrido[3,2-b]pyrazin-5(6H)-yl)heptanoic acid; 7-(2,3-bis(4-fluorophenyl)-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)heptanoic acid; 7-(2,3-di-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)heptanoic acid; 7-(2,3-bis(4-methoxyphenyl)-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)heptanoic acid; 6-(2,3-diphenyl-7,8-dihydropyrido[3,2-b]pyrazin-5(6H)-yl)hexanoic acid; and 5-(2,3-diphenyl-7,8-dihydropyrido[3,2-b]pyrazin-5(6H)-yl)pentanoic acid.
地址 Basel CH