IP Library › Granted Patent US 7,781,469
Granted Patent B2
US 7,781,469 · App. 11/920,999 · Granted Aug 24, 2010

Arylacetate derivatives having isoxazole skeleton

Assignee: Shionogi & Co., Ltd.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,781,469
App. No.
11/920,999
Granted
Aug 24, 2010
Kind
B2
Abstract

A compound of the formula (I): pharmaceutically acceptable salt or solvate thereof, wherein Y is a group of the formula: wherein Ring A is optionally substituted aryl or optionally substituted heteroaryl, X 3 is COOR 17 or the like Y is not optionally substituted phenyl which is substituted with the formula: —CR 9 R 10 X 3 at the para position, R 1 to R 10 are each independently halogen, hydroxy, optionally substituted lower alkyl, optionally substituted aryl or the like, X 1 is —O—, —S— or the like.

Claims (39)

1. A compound of the formula (I):

or a pharmaceutically acceptable salt thereof,

wherein:

Y is a group of the formula:

wherein

R 5 , R 6 , R 7 and R 8 are each independently hydrogen, halogen, hydroxy, cyano, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted lower alkoxy, optionally substituted lower alkylthio, optionally substituted acyl, optionally substituted amino, optionally substituted aryl, optionally substituted aryloxy, optionally substituted arylthio or optionally substituted heterocycle,

R 9 and R 10 are each independently hydrogen, halogen, cyano, optionally substituted lower alkyl, optionally substituted lower alkoxy, optionally substituted amino or optionally substituted aryl,

X 3 is COOR 17 or C(═NR 17 )NR 18 OR 19 ,

wherein R 17 , R 18 and R 19 are each independently hydrogen or optionally substituted lower alkyl,

R 1 is optionally substituted aryl or optionally substituted heterocycle,

R 2 is optionally substituted lower alkyl,

R 3 and R 4 are each independently hydrogen, halogen, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl or optionally substituted heterocycle, and

X 1 is O, S or —ON═CR 14 - wherein R 14 is hydrogen or optionally substituted lower alkyl.

2. The compound or pharmaceutically acceptable salt thereof according to claim 1 , wherein R 3 and R 4 are hydrogen.

3. The compound or pharmaceutically acceptable salt thereof according to claim 1 , wherein R 5 , R 6 , R 7 and R 8 are each independently hydrogen, halogen, optionally substituted lower akyl or optionally substituted lower alkoxy.

4. The compound or pharmaceutically acceptable salt thereof according to claim 1 , wherein R 9 and R 10 are each independently hydrogen or halogen.

5. The compound or pharmaceutically acceptable salt thereof according to claim 1 , wherein X 3 is COOR 17 wherein R 17 is hydrogen or optionally substituted lower alkyl.

6. The compound or pharmaceutically acceptable salt thereof according to claim 1 , wherein R 1 is optionally substituted aryl or heterocycle,

the substituent(s) of the aryl of R 1 is/are selected from the group consisting of halogen,

optionally substituted lower alkyl and optionally substituted lower alkoxy,

R 2 is optionally substituted lower alkyl,

the substituent(s) of the lower alkyl of R 2 is/are selected from the group consisting of optionally substituted lower alkoxy, lower alkylamino, optionally substituted imino, optionally substituted iminooxy, lower alkylsulfonyl, cycloalkyloxy, optionally substituted aryl and optionally substituted heterocycle,

R 3 and R 4 are hydrogen,

R 5 , R 6 , R 7 and R 8 are each independently, hydrogen, halogen, lower alkyl or lower alkoxy,

R 9 and R 10 are each independently hydrogen or halogen,

X 1 is O, S or —ON═CR 14 - wherein R 14 is hydrogen, and

X 3 is COOR 17 wherein R 17 is hydrogen or lower alkyl.

7. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to claim 1 as an active ingredient, and a pharmaceutically acceptable excipient and/or carrier.

8. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to claim 2 as an active ingredient, and a pharmaceutically acceptable excipient and/or carrier.

9. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to claim 3 as an active ingredient, and a pharmaceutically acceptable excipient and/or carrier.

10. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to claim 4 as an active ingredient, and a pharmaceutically acceptable excipient and/or carrier.

11. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to claim 5 as an active ingredient, and a pharmaceutically acceptable excipient and/or carrier.

12. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to claim 6 as an active ingredient, and a pharmaceutically acceptable excipient and/or carrier.

13. A method of treating hyperlipidemia, obesity, arteriosclerosis, atherosclerosis or hyperglycemia comprising administering an effective amount of the compound or pharmaceutically acceptable salt thereof according to claim 1 to a patient in need thereof.

14. A method of treating hyperlipidemia, obesity, arteriosclerosis, atherosclerosis or hyperglycemia comprising administering an effective amount of the compound or pharmaceutically acceptable salt thereof according to claim 2 to a patient in need thereof.

15. A method of treating hyperlipidemia, obesity, arteriosclerosis, atherosclerosis or hyperglycemia comprising administering an effective amount of the compound or pharmaceutically acceptable salt thereof according to claim 3 to a patient in need thereof.

16. A method of treating hyperlipidemia, obesity, arteriosclerosis, atherosclerosis or hyperglycemia comprising administering an effective amount of the compound or pharmaceutically acceptable salt thereof according to claim 4 to a patient in need thereof.

17. A method of treating hyperlipidemia, obesity, arteriosclerosis, atherosclerosis or hyperglycemia comprising administering an effective amount of the compound or pharmaceutically acceptable salt thereof according to claim 5 to a patient in need thereof.

18. A method of treating hyperlipidemia, obesity, arteriosclerosis, atherosclerosis or hyperglycemia comprising administering an effective amount of the compound or pharmaceutically acceptable salt thereof according to claim 6 to a patient in need thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2007
From: KANDA, YASUHIKO
To: SHIONOGI & CO., LTD.
Reel/Frame 020191/0339 →
Priority Claims (2)
JP 2005-155803 · May 27, 2005 · national
JP 2005-327171 · Nov 11, 2005 · national
Continuity (1)
Related Publication 20090062531A1 · Mar 5, 2009