发明名称 CaSR agonists
摘要 By searching various kinds of compounds having CaSR agonistic activity, the present invention provides CaSR agonistic agents, pharmaceutical compositions, preventive or therapeutic agents for diarrhea and kokumi-imparting agents each of which comprise the compound. More specifically, the present invention provides CaSR agonistic agents, pharmaceutical compositions, preventive or therapeutic agents for diarrhea and kokumi-imparting agents each of which comprise a glutamic acid derivative having CaSR agonistic activity or pharmaceutically acceptable salts thereof.
申请公布号 US9174932(B2) 申请公布日期 2015.11.03
申请号 US201414229152 申请日期 2014.03.28
申请人 AJINOMOTO CO., INC. 发明人 Sugiki Masayuki;Okamatsu Toru;Asari Sayaka;Kawato Yayoi;Hatanaka Toshihiro;Yano Tetsuo;Seki Yukie;Miyamura Naohiro;Nagasaki Hiroaki;Eto Yuzuru;Yasuda Reiko
分类号 C07C237/04;C07C309/51;C07F9/38;A23L1/228;A23L1/305;C07F9/40;A23L1/226 主分类号 C07C237/04
代理机构 Oblon, McClelland, Maier & Neustadt, L.L.P. 代理人 Oblon, McClelland, Maier & Neustadt, L.L.P.
主权项 1. A compound of formula (I) or a pharmaceutically acceptable salt thereof: wherein R1, R3, and R5 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, a hydroxyl group, —NH2, an optionally substituted alkyl group having 1 to 6 carbon atoms, and an optionally substituted alkoxy group having 1 to 6 carbon atoms; R4 is selected from the group consisting of a halogen atom, a hydroxyl group, —NH2, and an optionally substituted alkoxy group having 1 to 6 carbon atoms; R2 is selected from the group consisting of a sulfonic acid group, R6 and R7 are each independently a hydrogen atom or an optionally substituted alkyl group having 1 to 6 carbon atoms; and X is a methylene group or an oxygen atom; and excluding a compound wherein X is a methylene group, and R2 is
地址 Tokyo JP