Compounds, compositions, and methods for the treatment of synucleinopathies
View Patent ↗Bis- and tris-dihydroxyaryl compounds and their methylenedioxy analogs and pharmaceutically acceptable esters, their synthesis, pharmaceutical compositions containing them, and their use in the treatment of synucleinopathies, such as Parkinson's disease, and the manufacture of medicaments for such treatment.
1. A method of treating the formation, deposition, accumulation, or persistence of α-synuclein/NAC fibrils, comprising treating the fibrils with an effective amount of a compound of the formula:
or a pharmaceutically acceptable salt thereof, where:
R is a C 3 -C 10 alkylene group, in which:
a) there are optionally 1 or 2 non-adjacent double bonds;
b) 2 non-adjacent methylene groups are replaced by NR′, where R′ is H or alkyl; and
c) 1 or 2 methylene groups are replaced by a carbonyl group.
2. The method of claim 1 wherein the compound is selected from:
or a pharmaceutically acceptable salt thereof.
3. The method of claim 1 wherein treatment is provided to a mammal.
4. The method of claim 3 , wherein the mammal is a human.
5. The method of claim 1 , wherein the amount of the compound administered is between 0.1 mg/Kg/day and 1000 mg/Kg/day.
6. The method of claim 5 , wherein the amount of compound administered is between 1 mg/Kg/day and 100 mg/Kg/day.
7. The method of claim 5 , wherein the amount of compound administered is between 10 mg/Kg/day and 100 mg/Kg/day.
8. A method of inhibiting or relieving a synuclein disease, comprising administration of a therapeuticallv effective amount of a compound of the formula:
or a pharmaceutically acceptable salt thereof, where:
R is a C 3 -C 10 alkylene group, in which:
a) there are optionally 1 or 2 non-adjacent double bonds;
b) 2 non-adjacent methylene groups are replaced by NR′, where R′ is H or alkyl; and
c) 1 or 2 methylene groups are replaced by a carbonyl group.
9. The method of claim 8 , wherein the synuclein disease is selected from the group consisting of Parkinson's disease, familial Parkinson's disease, Lewy body disease, the Lewy body variant of Alzheimer's disease, dementia with Lewy bodies, multiple system atrophy, and the Parkinsonism-dementia complex of Guam.
10. The method of claim 8 , wherein the synuclein disease is Parkinson's disease.
11. The method of claim 8 , wherein the amount of the compound administered is between 0.1 mg/Kg/day and 1000 mg/Kg/day.
12. The method of claim 11 , wherein the amount of compound administered is between 1 mg/Kg/day and 100 mg/Kg/day.
13. The method of claim 11 , wherein the amount of compound administered is between 10 mg/Kg/day and 100 mg/Kg/day.
14. A method of providing neuroprotection from a synuclein disease to a mammal comprising the step of administrating a therapeutically effective amount of a compound of the formula:
or a pharmaceutically acceptable salt thereof, where:
R is a C 3 -C 10 alkylene group, in which:
a) there are optionally 1 or 2 non-adjacent double bonds;
b) 2 non-adjacent methylene groups are replaced by NR′, where R′ is H or alkyl; and
c) 1 or 2 methylene groups are replaced by a carbonyl group.
15. The method of claim 14 , wherein the synuclein disease is selected from the group consisting of Parkinson's disease, familial Parkinson's disease, Lewy body disease, the Lewy body variant of Alzheimer's disease, dementia with Lewy bodies, multiple system atrophy, and the Parkinsonism-dementia complex of Guam.
16. The method of claim 14 , wherein the synuclein disease is Parkinson's disease.
17. The method of claim 14 , wherein the amount of the compound administered is between 0.1 mg/Kg/day and 1000 mg/Kg/day.
18. The method of claim 17 , wherein the amount of compound administered is between 1 mg/Kg/day and 100 mg/Kg/day.
19. The method of claim 17 , wherein the amount of compound administered is between 10 mg/Kg/day and 100 mg/Kg/day.
20. The method of claim 14 wherein the therapeutically effective amount of compound administered is administered orally.