IP Library › Granted Patent US 9,845,305
Granted Patent B2
US 9,845,305 · App. 15/296,164 · Granted Dec 19, 2017

Treprostinil derivative compounds and methods of using same

Inventors: Cyrus K. Becker (Pleasanton, CA); Jürg R. Pfister (South San Francisco, CA); Gwenaella Rescourio (San Mateo, CA); Meenakshi S. Venkatraman (Fremont, CA); Xiaoming Zhang (Sunnyvale, CA)
Assignee: CORSAIR PHARMA, INC.
C07D321/00A61K9/0014A61K9/7023A61K31/165A61K31/216A61K31/341A61K31/365A61K45/06C07C59/72C07C69/712C07C69/734C07C69/74C07C69/96C07C219/16C07C235/20C07D207/08C07D211/60C07D257/06C07D263/24C07D263/26C07D265/30C07D295/088C07D295/145C07D307/20C07D317/34C07D317/40C07D453/02C07C2601/02C07C2601/08C07C2601/14C07C2602/42C07C2603/14
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Quick Facts
Patent No.
US 9,845,305
App. No.
15/296,164
Granted
Dec 19, 2017
Kind
B2
Abstract

Compounds represented by formulae I, II, III, and IV including pro-drugs for treprostinil and prostacyclin analogs. Uses include treatment of pulmonary hypertension (PH) or pulmonary arterial hypertension (PAH). The structures of the compounds can be adapted to the particular application for a suitable dosage. Transdermal applications can be used.

Claims (34)

1. A compound according to the following formula:

wherein:

R 20 , R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , R 27 , R 28 , R 29 , R 30 , R 31 , R 32 , R 33 , R 34 , R 35 and R 36 are independently H or deuterium;

Z is P 1 , wherein P 1 is selected from the group consisting of:

wherein:

m is 1, 2, 3 or 4;

R 14 and R 15 are independently in each occurrence selected from the group consisting of H, alkyl, cycloalkyl, alkylcycloalkyl, haloalkyl, heteroalkyl, substituted alkyl, aryl, heteroaryl, arylalkyl, heteroarylalkyl, substituted aryl, substituted heteroaryl, substituted arylalkyl, and substituted heteroarylalkyl; or

R 14 and R 15 taken together with the atoms to which they attach optionally form a 5- to 7-membered ring optionally incorporating one or two ring heteroatoms chosen from N, O and S, which is unsubstituted or substituted with 1, 2 or 3 substituents independently selected from the group consisting of halo, methyl and methoxy;

R 18 and R 19 are independently in each occurrence hydrogen or alkyl, wherein the alkyl is unsubstituted or substituted with 1 substituent selected from the group consisting of halo, hydroxy, alkoxy, amino, thio, methylthio, —C(O)OH, —C(O)O-(alkyl), —CONH 2 , aryl and heteroaryl, wherein the aryl or heteroaryl are unsubstituted or substituted with a substituent selected from the group consisting of alkyl, halo, haloalkyl, hydroxy, alkoxy, and haloalkoxy;

R 14 and R 18 taken together with the atoms to which they attach optionally form a 5- to 7-membered ring;

R 14 and R 19 taken together with the atoms to which they attach optionally form a 5- to 7-membered ring;

R 15 and R 18 taken together with the atoms to which they attach optionally form a 5- to 7-membered ring; and

R 15 and R 19 taken together with the atoms to which they attach optionally form a 5- to 7-membered ring; and

R 1 and R 2 are independently H or P 2 , wherein P 2 is selected from the group consisting of:

wherein:

m is 1, 2, 3 or 4; and

R 14 is independently in each occurrence selected from the group consisting of H, alkyl, cycloalkyl, alkylcycloalkyl, haloalkyl, heteroalkyl, substituted alkyl, aryl, heteroaryl, arylalkyl, heteroarylalkyl, substituted aryl, substituted heteroaryl, substituted arylalkyl, and substituted heteroarylalkyl;

or an enantiomer or a pharmaceutically acceptable salt thereof.

2. The compound of claim 1 , wherein R 1 is H and R 2 is P 2 .

3. The compound of claim 1 , wherein R 1 is P 2 and R 2 is H.

4. The compound of claim 1 , wherein R 1 is P 2 and R 2 is P 2 .

5. The compound of claim 1 , wherein R 1 and R 2 are each H.

6. The compound of claim 1 , wherein each of R 20 to R 36 is H.

7. The compound of claim 1 , wherein at least one of R 20 to R 36 is deuterium.

8. A composition comprising at least one compound according to claim 1 and at least one other component.

9. The composition of claim 8 , which is formulated for transdermal delivery.

10. The composition of claim 9 , which is formulated for transdermal delivery with a patch.

11. The composition of claim 8 , further comprising at least one solvent.

12. A method of treating pulmonary hypertension, comprising administering to a subject in need of treatment a therapeutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt, solvate, or enantiomer thereof.

13. The method of claim 12 , wherein the pulmonary hypertension is pulmonary arterial hypertension.

14. The method of claim 12 , wherein the compound is administered topically.

15. The method of claim 14 , wherein the compound is administered transdermally.

16. The method of claim 15 , wherein the compound is administered via a transdermal patch.

17. The method of claim 12 , further comprising administering an additional therapeutic agent selected from the group consisting of vasoactive agents, diuretics, anticoagulants and cardiac glycosides.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 11, 2024
From: BECKER, CYRUS K.; PFISTER, JÜRG R.; RESCOURIO, GWENAELLA; VENKATRAMAN, MEENAKSHI S.; ZHANG, XIAOMING
To: CORSAIR PHARMA, INC.
Reel/Frame 066101/0853 →
Continuity (4)
Continuation 14333456 · Jul 16, 2014
Continuation In Part 14153498 · Jan 13, 2014
Provisional Application 61751608 · Jan 11, 2013
Related Publication 20170081303A1 · Mar 23, 2017