发明名称 NOVEL ALIPHATIC COMPOUND, METHOD OF SYNTHESIS, AND METHOD OF UTILIZATION
摘要 <p>Fatty acid amide derivatives (I) are new. Fatty acid amide derivatives of formula (I) and their stereoisomers and salts are new. [Image] A : C nH (2n-2m)-CH 3; n : 4-22; m : number of unsaturated bonds and is 0-7; l : 0-10; s : 0; p+q : 4-5; or s : 1; and p+q : 3-4; R : 1-10C alkyl; and R AH or 1-10C alkyl. ACTIVITY : Antiaggregant; Antiinflammatory; Cardiant; Antiarteriosclerotic; Cerebroprotective; Vasotropic; Thrombolytic; Antianginal; Hepatotropic; Antilipemic. MECHANISM OF ACTION : Cytokine-Antagonist; TNF-Antagonist-alpha ; PDGF-Antagonist; Cholesterol-Antagonist. In assays, (4Z,7Z,10Z,13Z,16Z,19Z)-N-[2-(1-methylpyrrolidin-2-yl)ethyl]docosahexaenamide (Ia) inhibited platelet aggregation with an IC 5 0 of 1.5 MicroM, compared to 5.0 MicroM for indomethacin.</p>
申请公布号 EP1408030(A1) 申请公布日期 2004.04.14
申请号 EP20020738748 申请日期 2002.06.18
申请人 MARUHA CORPORATION 发明人 TAMAI, T.;YOSHIKAI, K.;NISHIKAWA, M.;OGASAWARA, KUNIO;MUROTA, I.
分类号 A61K31/40;A61K31/495;A61P9/00;A61P9/10;A61P29/00;C07D207/09;C07D295/32;(IPC1-7):C07D207/09;C07D295/22 主分类号 A61K31/40
代理机构 代理人
主权项
地址