发明名称 | Piperidinyl monocarboxylic acids as S1P1 receptor agonists | ||
摘要 | The present invention relates to novel compounds acting as agonists at S1P (sphingosine-1-phosphate) receptors, compositions containing these compounds, use of these compounds in medicine and their process of preparation.; | ||
申请公布号 | US9266867(B2) | 申请公布日期 | 2016.02.23 |
申请号 | US201214111438 | 申请日期 | 2012.04.10 |
申请人 | BIOPROJET;SUN PHARMA ADVANCED RESEARCH COMPANY LTD | 发明人 | Capet Marc;Berrebi-Bertrand Isabelle;Robert Philippe;Schwartz Jean-Charles;Lecomte Jeanne-Marie;Thennati Rajamannar;Pal Ranjan Kumar;Samanta Biswajit;Pillai Muthukumaran Natarajan;Desai Japan Nitinkumar;Rana Dijixa Chandubhai;Prajapati Kaushik Dhanjubhai;Pathak Sandeep Pankajbhai;Panchal Bhavesh M.;Aradhye Jayraj D. |
分类号 | C07D413/10;C07D271/06;A61K31/454;A61K45/06 | 主分类号 | C07D413/10 |
代理机构 | Stites & Harbison, PLLC | 代理人 | Schulman, Esq. B. Aaron;Stites & Harbison, PLLC |
主权项 | 1. A compound of formula (I): wherein: Ar is a phenyl group optionally substituted by one or more identical or different group(s) selected from the group consisting of halogen, alkyl, cycloalkyl, —Oalkyl, and phenyl; R1 represents —X—(Y)n— where —X— is selected from the group consisting of -alkyl-, -alkenyl-, -alkynyl-, -aryl-, and -alkylaryl-,each Y, identical or different is selected from the group consisting of H, OH, halogen, —Oalkyl, —Oalkylaryl, —OalkylOalkyl, —Oaryl, heteroaryl, —Oaryl(Oalkyl), —Ocycloalkyl, -cycloalkyl, and heterocyclyl;n is 1 to 3; and where R1 is not —C(═O)OH; and R2 is H or alkyl; or one of its stereoisomers or salts thereof. | ||
地址 | Paris FR |