发明名称 Amino acid derivatives
摘要 A compound of the formula (1): [wherein R1 is (substituted) alkyl, alkoxy, phenyl, hetero ring etc.; A is bond, CO, SO2; R2 is H, (substituted) alkyl etc.; D is alkylene etc.; E is COO, OCO, O, S, SO, SO2 etc.; R3 is (substituted) alkyl, carbocyclic ring, hetero ring; J is O, NR16 (R16 is H, substituted alkyl); R4 is (substituted) alkyl, carbocyclic ring, hetero ring.] 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 US2003013725(A1) 申请公布日期 2003.01.16
申请号 US20020154780 申请日期 2002.05.28
申请人 ONO PHARMACEUTICAL CO., LTD. 发明人 SEKO TAKUYA;KATO MASASHI
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):A61K31/505;A61K31/44;A61K31/24;A61K31/198 主分类号 A61K38/00
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