IP Library Granted Patent US 8,263,589
Granted Patent B2
US 8,263,589 · App. 12/294,605 · Granted Sep 11, 2012

Inhibitors of protein aggregation

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 8,263,589
App. No.
12/294,605
Granted
Sep 11, 2012
Kind
B2
Abstract

The invention relates generally to the use of diaminophenothiazine compounds to inhibit or reverse the aggregation of synuclein, and for their use in the manufacture of medicaments for this purpose (e.g. for the treatment of Parkinson's Disease). Also provided are related methods of detecting or labelling of aggregated synuclein.

Claims (81)

1. A method of treatment of a synucleinopathy, which synucleinopathy results in a neurodegenerative disease state and/or clinical dementia,

which method comprises orally administering to a subject a therapeutically effective amount of a diaminophenothiazine compound having the following formula:

wherein each one of R 1 , R 2 , R 4 , R 6 , R 8 , and R 9 is independently selected from:

—H;

—F; —Cl; —Br; —I;

—OH; —OR;

—SH; —SR;

—NO 2 ;

—C(═O)R;

—C(═O)OH; —C(═O)OR;

—C(═O)NH 2 ; —C(═O)NHR; —C(═O)NR 2 ; —C(═O)NR N1 R N2 ;

—NH 2 ; —NHR; —NR 2 ; —NR N1 R N2 ;

—NHC(═O)H; —NRC(═O)H; —NHC(═O)R; —NRC(═O)R; and

—R;

wherein each R is independently selected from:

unsubstituted aliphatic C 1-6 alkyl; substituted aliphatic C 1-6 alkyl;

unsubstituted aliphatic C 2-6 alkenyl; substituted aliphatic C 2-6 alkenyl;

unsubstituted C 3-6 cycloalkyl; substituted C 3-6 cycloalkyl;

unsubstituted C 6-10 -carboaryl; substituted C 6-10 carboaryl;

unsubstituted C 5-10 heteroaryl; substituted C 5-10 heteroaryl; and

unsubstituted C 6-10 -carboaryl-C 1-4 alkyl; substituted C 6-10 -carboaryl-C 1-4 alkyl;

wherein, in each group —NR N1 R N2 , independently, R N1 and R N2 taken together with the nitrogen atom to which they are attached form a ring having from 3 to 7 ring atoms;

each one of R 3NA and R 3NB is independently selected from:

—H;

unsubstituted aliphatic C 1-6 alkyl; substituted aliphatic C 1-6 alkyl;

unsubstituted aliphatic C 2-6 alkenyl; substituted aliphatic C 2-6 alkenyl;

unsubstituted C 3-6 cycloalkyl; substituted C 3-6 cycloalkyl;

unsubstituted C 6-10 -carboaryl; substituted C 6-10 -carboaryl;

unsubstituted C 5-10 heteroaryl; substituted C 5-10 heteroaryl; and

unsubstituted C 6-10 -carboaryl-C 1-4 alkyl; substituted C 6-10 -carboaryl-C 1-4 alkyl;

or: R 3NA and R 3NB taken together with the nitrogen atom to which they are attached form a ring having from 3 to 7 ring atoms;

and wherein the group —NR 7NA R 7NB is the same as the group —NR 3NA R 3NB :

and wherein X is one or more anionic counter ions to achieve electrical neutrality;

and pharmaceutically acceptable salts, mixed salts, and hydrates-thereof;

wherein the therapeutically effective amount of a diaminophenothizine compound orally administered to the subject is selected from the group consisting of

(i) a daily total dose of the diaminophenothizine compound orally administered to the subject of 200 mg-400 mg;

(ii) a daily total dose of the diaminophenothizine compound orally administered to the subject of 100 mg-400 mg;

(iii) in dosage units of about 10, 20, 30, 40, 50, 60, 80, 90, 100, 110, 120, or 130 mg three times a day; and

(iv) in dosage units of about 10, 20, 30, 40, 50, 60, 80, 90, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, or 200 mg twice a day.

2. The method according to claim 1 , wherein each one of R 1 , R 2 , R 4 , R 6 , R 8 , and R 9 is independently selected from: —H and —R.

3. The method according to claim 1 , wherein each one of R 1 , R 2 , R 4 , R 6 , R 8 , and R 9 is independently selected from: —H, -Me, -Et, -nPr, and -iPr.

4. The method according to claim 1 , wherein each of R 1 , R 2 , R 4 , R 6 , R 8 , and R 9 is —H.

5. The method according to claim 1 , wherein each one of R 3NA and R 3NB is independently selected from: —H, -Me, -Et, -nPr, and -iPr.

6. The method according to claim 5 , wherein each one of R 3NA and R 3NB is independently selected from: —H and -Me.

7. The method according to claim 1 , wherein X − is selected from Cl − , Br − , and I − .

8. The method according to claim 1 , wherein the compound is selected from the following compounds, and pharmaceutically acceptable salts, mixed salts, and hydrates thereof:

A

MTC

B

ETC

C

DMMTC

D

DEMTC

E

DMETC

F

DEETC

G

MTZ

H

ETZ

I

MTI

J

MTI.HI

K

ETI

L

ETI.HI

M

MTN

N

ETN

9. The method according to claim 1 wherein said treatment comprises orally administering to said subject said diaminophenothizine compound in combination with a compound that modulates dopamine levels in the subject.

10. The method according to claim 1 wherein a 400, 300, 200, or 100 mg daily total dose of said diaminophenothizine compound is orally administered to the subject.

11. The method according to claim 1 wherein the synuclein is α-synuclein.

12. The method according to claim 1 , wherein a daily total dose of the diaminophenothizine compound orally administered to the subject is 200 mg-400 mg.

13. The method according to claim 1 , wherein a daily total dose of the diaminophenothizine compound orally administered to the subject is 100 mg-400 mg.

14. The method according to claim 1 wherein the subject is orally administered the diaminophenothiazine compound in dosage units of about 10, 20, 30, 40, 50, 60, 80, 90, 100, 110, 120, or 130 mg three times a day.

15. The method according to claim 1 , wherein the subject is orally administered the diaminophenothiazine compound in dosage units of about 10, 20, 30, 40, 50, 60, 80, 90, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, or 200 mg twice a day.

Assignments (3)
CHANGE OF ADDRESS Recorded Jan 20, 2015
From: WISTA LABORATORIES LTD.
To: WISTA LABORATORIES LTD.
Reel/Frame 034781/0897 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 11, 2008
From: WISCHIK, CLAUDE MICHEL; RICKARD, JANET ELIZABETH; HARRINGTON, CHARLES ROBERT; HORSLEY, DAVID; THE UNIVERSITY COURT OF THE UNIVERSITY OF ABERDEEN
To: TAURX THERAPEUTICS LTD
Reel/Frame 021814/0308 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 11, 2008
From: TAURX THERAPEUTICS LTD
To: WISTA LABORATORIES LTD.
Reel/Frame 021814/0519 →