发明名称 AMINOSÄUREDERIVATE
摘要 A compound of the formula (I): <CHEM> Äwherein R<1> is (substituted) alkyl, alkoxy, phenyl, hetero ring etc.; A is bond, CO, SO2; R<2> is H, (substituted) alkyl etc.; D is alkylene etc.; E is COO, OCO, O, S, SO, SO2 etc.; R<3> is (substituted) alkyl, carbocyclic ring, hetero ring; J is O, NR<16> (R<16> is H, substituted alkyl); R<4> is (substituted) alkyl, carbocyclic ring, hetero ring.Ü or non-toxic salt thereof, and an N-type calcium channel blocker comprising it as an active ingredient. The compounds of the formula (I) possess an inhibitory action on N-type calcium channel, so they are useful as agent for the prevention and/or treatment of cerebral infarct, transient ischemic attack, encephalomyelopathy after cardiac operation, spinal angiopathy, hypertension with stress, neurosis or epilepsy etc. or agent for the treatment of pain.
申请公布号 AT320249(T) 申请公布日期 2006.04.15
申请号 AT19980929830T 申请日期 1998.07.03
申请人 ONO PHARMACEUTICAL CO., LTD. 发明人 SEKO, TAKUYA;CHOME, SHIMAMOTO-CHO;KATO, MASASHI;CHOME, SHIMAMOTO-CHO
分类号 A61K38/00;C07C233/46;C07C233/47;C07C233/51;C07C233/83;C07C235/52;C07C235/84;C07C237/08;C07C237/22;C07C237/36;C07C271/22;C07C309/18;C07C311/06;C07C311/13;C07C311/14;C07C311/19;C07C311/29;C07C311/46;C07C317/50;C07C323/59;C07C323/60;C07C323/62;C07D207/16;C07D211/14;C07D211/20;C07D211/58;C07D211/62;C07D213/30;C07D213/32;C07D213/64;C07D213/643;C07D213/75;C07D213/81;C07D213/82;C07D215/06;C07D215/08;C07D215/12;C07D217/06;C07D233/54;C07D233/90;C07D263/34;C07D277/04;C07D277/06;C07D277/14;C07D277/16;C07D277/56;C07D279/06;C07D279/12;C07D295/135;C07D295/185;C07D307/14;C07D307/24;C07D307/42;C07D307/52;C07D307/68;C07D309/04;C07D309/06;C07D333/16;C07D333/20;C07D333/38;C07D417/12;C07K5/072;C07K5/078;(IPC1-7):A61K31/165;A61K31/42;A61K31/38;A61K31/27;A61K31/215;A61K31/18;A61K31/425;A61K31/34 主分类号 A61K38/00
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