IP Library Granted Patent US 9,586,896
Granted Patent B2
US 9,586,896 · App. 14/880,173 · Granted Mar 7, 2017

Nitroxyl donors with improved therapeutic index

Inventors: Vincent Jacob Kalish (Annapolis, MD); Frederick Arthur Brookfield (Abingdon, GB); Stephen Martin Courtney (Abingdon, GB); Lisa Marie Frost (Abingdon, GB); John P. Toscano (Glen Arm, MD)
Assignee: Cardioxyl Pharmaceuticals, Inc.
C07C317/14A61K31/18A61K31/222A61K31/24A61K31/255A61K31/341A61K31/343A61K31/381A61K31/404A61K31/42A61K31/433A61K31/4436A61K31/538A61K31/5377A61K47/12A61K47/40C07D307/64
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Quick Facts
Patent No.
US 9,586,896
App. No.
14/880,173
Granted
Mar 7, 2017
Kind
B2
Abstract

The disclosed subject matter provides N-substituted hydroxylamine derivative compounds, pharmaceutical compositions and kits comprising such compounds, and methods of using such compounds or pharmaceutical compositions. In particular, the disclosed subject matter provides methods of using such compounds or pharmaceutical compositions for treating heart failure.

Claims (26)

1. A compound of formula (4):

wherein

R is hydrogen, —(C 2 -C 4 )alkenyl, phenyl, benzyl, cyclopentyl, cyclohexyl, —(C 5 -C 7 )heterocycloalkyl, benzyloxy, —O—(C 1 -C 6 )alkyl, —NH 2 , —NH—(C 1 -C 4 )alkyl, or —N((C 1 -C 4 )alkyl) 2 ,

wherein said —(C 2 -C 4 )alkenyl, phenyl, benzyl, cyclopentyl, cyclohexyl, —(C 5 -C 7 )heterocycloalkyl, benzyloxy, —O—(C 1 -C 6 )alkyl, —NH—(C 1 -C 4 )alkyl, or —N((C 1 -C 4 )alkyl) 2 can be unsubstituted or substituted with one or more substituents selected from halo, —(C 1 -C 6 )alkyl, —(C 2 -C 4 )alkenyl, —(C 2 -C 3 )alkynyl, —(5—or 6—membered)heteroaryl, —O—(C 1 -C 6 )alkyl, —S—(C 1 -C 6 )alkyl, —C(halo) 3, —CH(halo) 2 , —CH 2 (halo), —CN, —NO 2 , —NH 2 , —NH—(C 1 -C 4 )alkyl, —N(—(C 1 -C 4 )alkyl) 2 , —C(=O)(C 1 -C 4 )alkyl, —C(═O)(C 1 -C 4 )alkyl, —OC(═O)(C 1 -C 4 )alkyl, —OC(═O)NH 2 , —S(═O)(C 1 -C 4 )alkyl, or —S(═O) 2 (C 1 -C 4 )alkyl.

2. The compound of claim 1 , wherein R is benzyl or phenyl.

3. The compound of claim 1 , wherein R is phenyl.

4. The compound of claim 1 , wherein R is benzyl.

5. The compound of claim 1 , wherein R is —NH 2 .

6. The compound of claim 1 , wherein R is unsubstituted.

7. The compound of claim 1 , wherein R is substituted with a substituent selected from -halo, —NH 2 , —NHCH 3 , —CF 3 , or —OCH 3 .

8. A method of treating a cardiovascular disease, comprising administering an effective amount of the compound of claim 1 to a patient in need thereof.

9. The method of claim 8 , wherein the compound is administered intravenously.

10. The method of claim 8 , wherein the cardiovascular disease is heart failure.

11. The method of claim 10 , wherein the compound is administered intravenously.

12. The method of claim 8 , wherein the cardiovascular disease is acute decompensated heart failure.

13. The method of claim 12 , wherein the compound is administered intravenously.

14. A pharmaceutical composition comprising the compound of claim 1 and at least one pharmaceutically acceptable excipient.

15. The pharmaceutical composition of claim 14 , wherein the pharmaceutical composition is suitable for intravenous administration.

16. The pharmaceutical composition of claim 14 , wherein the at least one pharmaceutically acceptable excipient is at least one species of cyclodextrin.

17. The pharmaceutical composition of claim 16 , wherein the pharmaceutical composition is suitable for intravenous administration.

18. A method of treating a cardiovascular disease, comprising administering an effective amount of the pharmaceutical composition of claim 14 a patient in need thereof.

19. The method of claim 18 , wherein the pharmaceutical composition is administered intravenously.

20. The method of claim 18 , wherein the cardiovascular disease is heart failure.

21. The method of claim 20 , wherein the pharmaceutical composition is administered intravenously.

22. The method of claim 18 , wherein the cardiovascular disease is acute decompensated heart failure.

23. The method of claim 22 , wherein the pharmaceutical composition is administered intravenously.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 13, 2015
From: KALISH, VINCENT JACOB; TOSCANO, JOHN P.; BROOKFIELD, FREDERICK ARTHUR; COURTNEY, STEPHEN MARTIN; FROST, LISA MARIE
To: CARDIOXYL PHARMACEUTICALS, INC.
Reel/Frame 036778/0520 →
Continuity (5)
Continuation 14641377 · Mar 7, 2015
Continuation 14158456 · Jan 17, 2014
Provisional Application 61782781 · Mar 14, 2013
Provisional Application 61754237 · Jan 18, 2013
Related Publication 20160031807A1 · Feb 4, 2016