发明名称 NOVEL COMPOUNDS FOR MEDICAL USE AS PEPTIDASE EFFECTORS
摘要 <P>PROBLEM TO BE SOLVED: To provide a novel compound which can concertedly inhibit ectoenzymes dipeptidyl peptidase IV (DPIV) and alanyl aminopeptidase (APN) cooperatively. <P>SOLUTION: The compound is a compound of formula (I) or an acid addition salt with an organic acid and/or inorganic acid. (In the formula, residues R1, R2, R3 and R4 may be the same or different, -H, >C(=O), -C(=O)O- and the like; E represents -O-, -S-, -NH- and the like; Y represents -O-, -NH- and the like; B represents an alkyl substituted group or an alkoxy substituted group having an aryl group or a heterocyclic ring; and C represents a substitution group having amide bond or sulfonamide bond). <P>COPYRIGHT: (C)2012,JPO&INPIT
申请公布号 JP2012031170(A) 申请公布日期 2012.02.16
申请号 JP20110162967 申请日期 2011.07.26
申请人 IMTM GMBH 发明人 ANSORGE SIEGFRIED;BANK UTE;HEIMBURG ANTJE;JULIUS HEIKO;NORDHOFF CARSTEN;TAEGER MICHAEL
分类号 C07C237/10;A61K8/42;A61K8/44;A61K8/46;A61K8/49;A61K8/58;A61K31/165;A61K31/167;A61K31/18;A61K31/221;A61K31/27;A61K31/405;A61K31/4245;A61K31/425;A61K31/427;A61K31/4418;A61K31/505;A61K31/52;A61K31/695;A61K45/00;A61P1/00;A61P1/04;A61P3/10;A61P9/10;A61P11/00;A61P11/06;A61P17/00;A61P17/02;A61P17/06;A61P17/10;A61P19/02;A61P21/02;A61P25/00;A61P25/14;A61P25/16;A61P25/28;A61P29/00;A61P31/04;A61P31/12;A61P31/14;A61P33/06;A61P35/00;A61P35/04;A61P37/02;A61P37/06;A61P37/08;A61P43/00;A61Q19/00;C07C271/20;C07C311/32;C07C311/35;C07C311/41;C07D209/08;C07D209/20;C07D213/30;C07D213/56;C07D239/26;C07D271/12;C07D277/04;C07D417/12;C07D473/00;C07F7/18 主分类号 C07C237/10
代理机构 代理人
主权项
地址