IP Library Granted Patent US 8,796,485
Granted Patent B2
US 8,796,485 · App. 13/079,273 · Granted Aug 5, 2014

CaSR agonists

Inventors: Masayuki Sugiki (Kawasaki, JP); Toru Okamatsu (Kawasaki, JP); Sayaka Asari (Kawasaki, JP); Yayoi Kawato (Kawasaki, JP); Toshihiro Hatanaka (Kawasaki, JP); Tetsuo Yano (Kawasaki, JP); Yukie Seki (Kawasaki, JP); Naohiro Miyamura (Kawasaki, JP); Hiroaki Nagasaki (Kawasaki, JP); Yuzuru Eto (Kawasaki, JP); Reiko Yasuda (Kawasaki, JP)
Assignee: Ajinomoto Co., Inc.
C07F9/3834C07C309/51C07F9/4021C07C237/04A23L1/228A23L1/3051
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Quick Facts
Patent No.
US 8,796,485
App. No.
13/079,273
Granted
Aug 5, 2014
Kind
B2
Abstract

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.

Claims (15)

1. A glutamic acid derivative of formula (I) or a pharmaceutically acceptable thereof:

wherein R 1 and R 3 -R 5 are each independently selected from the group consisting of a hydrogen atom, a halogeno group, a hydroxyl group, a nitro group, —NH 2 , an optionally substituted alkyl group having 1 to 6 carbon atoms, and an optionally substituted alkoxy group having 1 to 6 carbon atoms;

R 2 is selected from the group consisting of a nitro group, a sulfonic acid group,

R 6 is a hydroxyl group;

R 7 is 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.

2. A pharmaceutical composition comprising a glutamic acid derivative of formula (I) or a pharmaceutically acceptable salt thereof:

wherein R 1 and R 3 -R 5 are each independently selected from the group consisting of a hydrogen atom, a halogeno group, a hydroxyl group, —NH 2 , an optionally substituted alkyl group having 1 to 6 carbon atoms, and an optionally substituted alkoxy group having 1 to 6 carbon atoms;

R 2 is selected from the group consisting of a sulfonic acid group,

R 6 and R 7 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, R 2 is

3. A pharmaceutical composition comprising the glutamic acid derivative or pharmaceutically acceptable salt thereof according to claim 1 and a pharmaceutically acceptable carrier.

4. The glutamic acid derivative or pharmaceutically acceptable salt thereof of claim 1 , wherein X is methylene.

5. The glutamic acid derivative or pharmaceutically acceptable salt thereof of claim 2 , wherein X is methylene.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 21, 2016
From: AJINOMOTO CO., INC.
To: EA PHARMA CO., LTD.
Reel/Frame 039094/0087 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2011
From: SUGIKI, MASAYUKI; OKAMATSU, TORU; ASARI, SAYAKA; KAWATO, YAYOI; HATANAKA, TOSHIHIRO; YANO, TETSUO; SEKI, YUKIE; MIYAMURA, NAOHIRO; NAGASAKI, HIROAKI; ETO, YUZURU; YASUDA, REIKO
To: AJINOMOTO CO., INC.
Reel/Frame 026456/0402 →
Priority Claims (1)
JP 2008-258003 · Oct 3, 2008 · national
Continuity (2)
Continuation PCTJP2009067342 · Oct 5, 2009
Related Publication 20110251418A1 · Oct 13, 2011