IP Library › Granted Patent US 10,858,358
Granted Patent B2
US 10,858,358 · App. 16/586,498 · Granted Dec 8, 2020

S1PR2 antagonists and uses therefor

Inventors: Christopher McMaster (Halifax, CA); Gordon Simms (Halifax, CA)
Assignee: DALHOUSIE UNIVERSITY
C07D471/04A61K31/444A61P3/10A61P9/00A61P9/10A61P9/12A61P11/00A61P15/00A61P19/10A61P25/00A61P25/28A61P27/02C07C229/24C07C317/48C07F9/3808C07J31/006C07F9/091C07F9/65583
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 10,858,358
App. No.
16/586,498
Granted
Dec 8, 2020
Kind
B2
Abstract

Methods and compositions are provided for the treatment of familial exudative vitreoretinopathy (FEVR) through the administration of a therapeutically effective amount of a sphingosine-1-phosphate receptor type 2 (S1PR2) antagonist. Also provided herein are (Z)-2-cyano-1-(2,6-dichloropyridin-4-yl)-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)guanidine and analogs thereof, and their use in treating retinopathies and diseases characterized by insufficient angiogenesis.

Claims (72)

1. A compound of formula (XII):

or a pharmaceutically acceptable salt thereof,

wherein:

G 1 is CR 12 or NR 13 , wherein R 12 and R 13 are each independently selected from the group consisting of H, C 1 -C 4 alkyl, and benzyl;

R c and R d are independently selected from the group consisting of H, C 1 -C 4 alkyl, and benzyl; or R c and R d are joined to form a 5- or 6-membered heterocycloalkyl ring; and,

the cyano group is in the (Z) or (E) configuration.

2. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein:

G 1 is CR 12 and R 12 is H; and,

R d is H.

3. The compound of claim 2 , selected from the group consisting of:

(E)-2-cyano-3-(2,6-dichloropyridin-4-yl)-1-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)-1-methylguanidine;

(E)-2-cyano-3-(2,6-dichloropyridin-4-yl)-1-ethyl-1-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)guanidine;

(E)-2-cyano-3-(2,6-dichloropyridin-4-yl)-1-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)-1-propylguanidine;

(E)-1-butyl-2-cyano-3-(2,6-dichloropyridin-4-yl)-1-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)guanidine;

(E)-2-cyano-3-(2,6-dichloropyridin-4-yl)-1-isopropyl-1-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)guanidine;

(E)-1-benzyl-2-cyano-3-(2,6-dichloropyridin-4-yl)-1-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)guanidine; and,

a diastereomer of the foregoing, wherein the cyano group is in the (Z) form; or the pharmaceutically acceptable salt of any of the foregoing.

4. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein:

G 1 is CR 12 and R 12 is H; and,

R c is H.

5. The compound of claim 4 , selected from the group consisting of:

(Z)-2-cyano-1-(2,6-dichloropyridin-4-yl)-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)-1-methylguanidine;

(Z)-2-cyano-1-(2,6-dichloropyridin-4-yl)-1-ethyl-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)guanidine;

(Z)-2-cyano-1-(2,6-dichloropyridin-4-yl)-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)-1-propylguanidine;

(Z)-1-butyl-2-cyano-1-(2,6-dichloropyridin-4-yl)-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)guanidine;

(Z)-2-cyano-1-(2,6-dichloropyridin-4-yl)-1-isopropyl-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)guanidine;

(Z)-1-benzyl-2-cyano-1-(2,6-dichloropyridin-4-yl)-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)guanidine; and,

a diastereomer of the foregoing, wherein the cyano group is in the (E) form; or the pharmaceutically acceptable salt of any of the foregoing.

6. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein:

G 1 is CR 12 ; and,

R c and R d are each H.

7. The compound of claim 6 , selected from the group consisting of:

(Z)-2-cyano-1-(2,6-dichloropyridin-4-yl)-3-(1-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)ethyl)guanidine;

(Z)-2-cyano-1-(2,6-dichloropyridin-4-yl)-3-(1-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)propyl)guanidine;

(Z)-2-cyano-1-(2,6-dichloropyridin-4-yl)-3-(1-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)-2-methylpropyl)guanidine;

(Z)-2-cyano-1-(2,6-dichloropyridin-4-yl)-3-(1-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)-2-phenylethyl)guanidine; and,

a diastereomer of the foregoing, wherein the cyano group is in the (E) form; or the pharmaceutically acceptable salt of any of the foregoing.

8. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein:

G 1 is NR 13 ; and,

R c and R d are each H.

9. The compound of claim 8 , selected from the group consisting of:

(E)-N′-cyano-N-(2,6-dichloropyridin-4-yl)-2-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)hydrazinecarboximidamide;

(E)-N′-cyano-N-(2,6-dichloropyridin-4-yl)-2-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)-2-methylhydrazinecarboximidamide;

(E)-N′-cyano-N-(2,6-dichloropyridin-4-yl)-2-ethyl-2-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)hydrazinecarboximidamide;

(E)-N′-cyano-N-(2,6-dichloropyridin-4-yl)-2-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)-2-propylhydrazinecarboximidamide;

(E)-2-butyl-N′-cyano-N-(2,6-dichloropyridin-4-yl)-2-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)hydrazinecarboximidamide;

(E)-N′-cyano-N-(2,6-dichloropyridin-4-yl)-2-isopropyl-2-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)hydrazinecarboximidamide;

(E)-2-b enzyl-N′-cyano-N-(2,6-dichloropyridin-4-yl)-2-(4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)hydrazinecarboximidamide; and,

a diastereomer of the foregoing, wherein the cyano group is in the (Z) form; or the pharmaceutically acceptable salt of any of the foregoing.

10. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein:

G 1 is CR 12 and R 12 is H.

11. The compound of claim 10 , selected from the group consisting of:

(Z)-2-cyano-1-(2,6-dichloropyridin-4-yl)-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)-1,3-dimethylguanidine;

(Z)-2-cyano-1-(2,6-dichloropyridin-4-yl)-3-isopropyl-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)-1-methylguanidine;

(Z)-2-cyano-1-(2,6-dichloropyridin-4-yl)-1-isopropyl-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)-3-methylguanidine;

(Z)-1-benzyl-2-cyano-3-(2,6-dichloropyridin-4-yl)-1-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)-3-methylguanidine;

(Z)-1-benzyl-2-cyano-1-(2,6-dichloropyridin-4-yl)-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)-3-methylguanidine; and,

a diastereomer of the foregoing, wherein the cyano group is in the (E) form; or the pharmaceutically acceptable salt of any of the foregoing.

12. The compound or pharmaceutically acceptable salt thereof of claim 1 , wherein:

G 1 is CR 12 and CR 12 is H; and,

R c and R d are joined to form a 5- or 6-membered heterocycloalkyl ring.

13. The compound of claim 12 , selected from the group consisting of:

(Z)—N-(1-(2,6-dichloropyridin-4-yl)-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)tetrahydropyrimidin-2(1H)-ylidene)cyanamide;

(Z)—N-(1-(2,6-dichloropyridin-4-yl)-3-((4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yl)methyl)imidazolidin-2-ylidene)cyanamide; and,

a diastereomer of the foregoing, wherein the cyano group is in the (E) form; or the pharmaceutically acceptable salt of any of the foregoing.

14. A method of treating an eye condition in a subject in need thereof, comprising administering to the subject a pharmaceutically effective amount of the compound of claim 1 , or a pharmaceutically-acceptable salt thereof.

15. The method of claim 14 , wherein the eye condition is caused by a primary defect in retinal vascularization followed by secondary aberrant neovascularization that can result in retina detachment.

16. The method of claim 14 , wherein the eye condition is a retinopathy.

17. The method of claim 16 , wherein the retinopathy is selected from the group consisting of diabetic retinopathy, macular degeneration, hypertensive retinopathy, radiation retinopathy, solar retinopathy, retinopathy of prematurity (ROP), Norrie disease (ND), familial exudative vitreoretinopathy (FEVR), Coats' disease, sickle cell retinopathy, and retinitis pigmentosa.

18. The method of claim 17 , wherein the retinopathy is FEVR.

19. A method of treating a disease characterized by insufficient angiogenesis in a subject in need thereof, comprising administering to the subject a pharmaceutically effective amount of the compound of claim 1 , or a pharmaceutically-acceptable salt thereof.

20. The method of claim 19 , wherein the disease is selected from the group consisting of atherosclerosis, hypertension, diabetes, restenosis, pre-eclampsia, menorrhagia, neonatal respiratory distress, pulmonary fibrosis, nephropathy, osteoporosis, amyotrophic lateral sclerosis, stroke, and Alzheimer's disease.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 8, 2020
From: MCMASTER, CHRISTOPHER; SIMMS, GORDON
To: DALHOUSIE UNIVERSITY
Reel/Frame 053154/0882 →
Continuity (5)
Continuation In Part 16269339 · Feb 6, 2019
Continuation In Part 16234014 · Dec 27, 2018
Continuation 15578998
Provisional Application 62169375 · Jun 1, 2015
Related Publication 20200017494A1 · Jan 16, 2020