Inhibitors of protein aggregation
View Patent ↗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.
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.