发明名称 Rho KINASE INHIBITOR COMPRISING AMIDE COMPOUND
摘要 PROBLEM TO BE SOLVED: To provide a therapeutic agent having markedly and selectively Rho kinase-inhibitory activity, free from any problematic toxicity, having favorable oral absorbability and pharmacokinetics (medicinal absorption, distribution, metabolism and excretion) and good physical properties (e.g. stability) in terms of compound, and useful for various diseases involving Rho kinase. SOLUTION: The objective Rho kinase inhibitor comprises an amide compound of the general formula (I) [where, Ra is a (substituted) nitrogen-containing heterocyclic ring; Rb is H or the like; and Rc is an aryl bearing 1-5 substituent(s) being the same or different, or the like]. An isomer thereof or a pharmaceutically acceptable salt thereof is an option of the inhibitor.
申请公布号 JP2003073357(A) 申请公布日期 2003.03.12
申请号 JP20010266055 申请日期 2001.09.03
申请人 MITSUBISHI PHARMA CORP 发明人 UEHATA MASAYOSHI;TAKANASHI SHINICHI;HAMAGUCHI SEISHI
分类号 G01N33/50;A61K31/437;A61K31/4409;A61K31/4427;A61K31/4436;A61K31/444;A61K31/4725;A61K31/5025;A61K31/538;A61P1/00;A61P9/00;A61P9/04;A61P9/08;A61P9/10;A61P9/12;A61P11/00;A61P11/06;A61P15/00;A61P15/06;A61P15/10;A61P19/08;A61P25/00;A61P25/28;A61P27/02;A61P27/06;A61P29/00;A61P31/18;A61P35/00;A61P35/04;A61P37/06;A61P43/00;C07D213/75;C07D403/12;C07D405/12;C07D409/12;C07D471/04;C07D487/04;C07D495/04;(IPC1-7):C07D213/75;A61K31/440;A61K31/442;A61K31/443;A61K31/472;A61K31/502 主分类号 G01N33/50
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