IP Library Granted Patent US 7,943,613
Granted Patent B2
US 7,943,613 · App. 12/097,564 · Granted May 17, 2011

Compounds, their preparation and use

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Quick Facts
Patent No.
US 7,943,613
App. No.
12/097,564
Granted
May 17, 2011
Kind
B2
Abstract

Novel compounds of the general formula (I), the use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds and methods of treatment employing these compounds and compositions. The present compounds are activators of PPARδ and should be useful for treating conditions mediated by the same.

Claims (35)

1. (E)-[4-[3-(4-Fluorophenyl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]allyloxy]-2-methyl-phenoxy]acetic acid or a pharmaceutically acceptable salt thereof.

2. The compound of claim 1 , where the compound is (E)-[4-[3-(4-fluorophenyl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]allyloxy]-2-methyl-phenoxy]acetic acid.

3. The compound of claim 1 , where the compound is a pharmaceutically acceptable salt of (E)-[4-[3-(4-fluorophenyl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]allyloxy]-2-methyl-phenoxy]acetic acid.

4. The compound of claim 3 , where the pharmaceutically acceptable salt of (E)-[4-[3-(4-fluorophenyl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]allyloxy]-2-methyl-phenoxy]acetic acid is selected from the group consisting of a sodium salt, a potassium salt, a magnesium salt, and a calcium salt.

5. The compound of claim 4 , where the compound is a sodium salt of (E)-[4-[3-(4-fluorophenyl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]allyloxy]-2-methyl-phenoxy]acetic acid.

6. (Z)-[4-[3-(4-Fluorophenyl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]allyloxy]-2-methyl-phenoxy]acetic acid or a pharmaceutically acceptable salt thereof.

7. The compound of claim 6 , where the compound is (Z)-[4-[3-(4-fluorophenyl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]allyloxy]-2-methyl-phenoxy]acetic acid.

8. The compound of claim 6 , where the compound is a pharmaceutically acceptable salt of (Z)-[4-[3-(4-fluorophenyl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]allyloxy]-2-methyl-phenoxy]acetic acid.

9. The compound of claim 8 , where the pharmaceutically acceptable salt of (Z)-[4-[3-(4-fluorophenyl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]allyloxy]-2-methyl-phenoxy]acetic acid is selected from the group consisting of a sodium salt, a potassium salt, a magnesium salt, and a calcium salt.

10. The compound of claim 9 , where the compound is a sodium salt of (Z)-[4-[3-(4-fluorophenyl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]allyloxy]-2-methyl-phenoxy]acetic acid.

11. A pharmaceutical composition comprising a compound according to claim 1 and a pharmaceutically acceptable carrier or excipient.

12. A pharmaceutical composition comprising a compound according to claim 2 and a pharmaceutically acceptable carrier or excipient.

13. A pharmaceutical composition comprising a compound according to claim 3 and a pharmaceutically acceptable carrier or excipient.

14. A pharmaceutical composition comprising a compound according to claim 4 and a pharmaceutically acceptable carrier or excipient.

15. A pharmaceutical composition comprising a compound according to claim 5 and a pharmaceutically acceptable carrier or excipient.

16. A pharmaceutical composition comprising a compound according to claim 6 and a pharmaceutically acceptable carrier or excipient.

17. A pharmaceutical composition comprising a compound according to claim 7 and a pharmaceutically acceptable carrier or excipient.

18. A pharmaceutical composition comprising a compound according to claim 8 and a pharmaceutically acceptable carrier or excipient.

19. A pharmaceutical composition comprising a compound according to claim 9 and a pharmaceutically acceptable carrier or excipient.

20. A pharmaceutical composition comprising a compound according to claim 10 and a pharmaceutically acceptable carrier or excipient.

21. A compound of formula (I) or a pharmaceutically acceptable salt thereof:

wherein is a double bond, with either E or Z substitution;

X 1 is C 1-6 -alkyl substituted with morpholino;

X 2 is phenylene;

X 3 is phenyl substituted with one or more halogens;

Ar is phenylene optionally substituted with methyl;

Y 1 is O;

Y 2 is O;

Z is CH 2 ;

R 1 is H; and

R 2 is H;

or a hydrate of any of the foregoing.

22. The compound of claim 21 wherein X 1 is morpholin-4-ylmethyl.

23. A pharmaceutical composition comprising a compound according to claim 21 and a pharmaceutically acceptable carrier or excipient.

24. A pharmaceutical composition comprising a compound according to claim 22 and a pharmaceutically acceptable carrier or excipient.

Assignments (7)
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY DATA PREVIOUSLY RECORDED AT REEL: 036254 FRAME: 0792. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Sep 24, 2015
From: M&F TTP HOLDINGS LLC, AS COLLATERAL AGENT
To: VTVX HOLDINGS II LLC
Reel/Frame 036675/0399 →
RELEASE OF SECURITY INTEREST Recorded Aug 3, 2015
From: M&F TTP HOLDINGS LLC, AS COLLATERAL AGENT
To: VTVX HOLDINGS I LLC
Reel/Frame 036254/0792 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2015
From: VTVX HOLDINGS II LLC
To: VTV THERAPEUTICS LLC
Reel/Frame 036242/0362 →
CHANGE OF NAME Recorded Jul 30, 2015
From: HIGH POINT PHARMACEUTICALS, LLC
To: VTVX HOLDINGS II LLC
Reel/Frame 036236/0159 →
SECURITY INTEREST Recorded Feb 26, 2015
From: HIGH POINT PHARMACEUTICALS, LLC
To: M&F TTP HOLDINGS LLC, AS COLLATERAL AGENT
Reel/Frame 035103/0029 →
NOTICE OF RELEASE OF SECURITY INTEREST IN PATENTS FOR REEL/FRAME 030982/0793 Recorded Apr 7, 2014
From: M&F TTP HOLDINGS LLC
To: HIGH POINT PHARMACEUTICALS, LLC
Reel/Frame 032621/0867 →
SECURITY AGREEMENT Recorded Aug 9, 2013
From: HIGH POINT PHARMACEUTICALS, LLC
To: M&F TTP HOLDINGS LLC C/O MACANDREWS & FORBES HOLDINGS INC.
Reel/Frame 030982/0793 →