Novel methods of treating hearing loss
US-2024390323-A1 · Nov 28, 2024 · US
US10188659B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10188659-B2 |
| Application number | US-201715685244-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 24, 2017 |
| Priority date | Jul 14, 2013 |
| Publication date | Jan 29, 2019 |
| Grant date | Jan 29, 2019 |
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The present invention provides compounds acting as Insulin/IGF signaling modulators useful in the treatment of neurodegenerative diseases and disorders. The invention provides pharmaceutical compositions including such compounds, and methods of using these compounds and compositions for the treatment of neurodegenerative diseases, in particular neurodegenerative diseases caused by proteotoxicity such as Alzheimer's disease.
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The invention claimed is: 1. A method of inhibiting toxic protein aggregation in a subject having a neurodegenerative disease selected from the group consisting of Amyloidosis, Prion disorders, Motor Neuron disease, Alzheimer's disease, Fronto temporal dementia 17 (FTD17), Huntington disease and Parkinson's disease, the method comprising the step of administering to the subject a therapeutically effective amount of a compound represented by the structure of formula I: wherein A is H or CN; Z is S, SO or SO 2 ; X 1 , X 2 , X 3 , X 4 , X 5 , Y 1 and Y 2 are each independently selected from H, halogen, alkyl, haloalkyl and OR 1 ; and Y 3 and Y 4 are each OR 1 , wherein each R 1 is independently H, C 1 -C 4 alkyl, acyl, —(CH 2 CH 2 O) n H wherein n is an integer of 1 to 20, or a functional group that gives rise to hydroxyl upon hydrolysis, or salts, hydrates, and solvates thereof. 2. The method of claim 1 , wherein the compound is selected from the group consisting of: or salts, hydrates, and solvates thereof. 3. The method of claim 2 , comprising administering to a subject in need thereof a therapeutically effective amount of compound no. 4 or salts, hydrates, and solvates thereof. 4. The method of claim 1 , wherein in compound I: (a) X 3 is Br, Cl, I or CF 3 ; (b) X 1 and X 2 are each Br; or (c) X 1 is CF 3 . 5. The method of claim 1 , wherein Amyloidosis is selected from the group consisting of AL amyloidosis, AA amyloidosis, familial amyloid polyneuropathies, senile systemic amyloidosis, Leptomeningeal amyloidosis, Haemodialysis-associated amyloidosis, Finnish type amyloidosis, Cerebral amyloid angiopathy; Familial visceral amyloidosis; Familial corneal amyloidosis; Primary cutaneous amyloidosis and Senile amyloid of atria of heart. 6. The method of claim 1 , wherein the prion disorders are selected from the group consisting of Finnish type amyloidosis; Creutzfeldt-Jakob disease, fatal familial insomnia (FFI) and Gerstmann-Straussler-Scheinker syndrome (GSS). 7. The method of claim 1 , wherein the neurodegenerative disease is caused by toxic amyloid beta (Aβ) aggregation. 8. The method of claim 7 , wherein the neurodegenerative disease is Alzheimer's disease. 9. The method of claim 1 , wherein the compound inhibits IGF1 signaling. 10. The method of claim 1 , wherein the compound is compound no. 4 or salts, hydrates and solvates thereof, and wherein the neurodegenerative disease is Alzheimer's disease. 11. The method of claim 1 , wherein the compound is compound no. 4 or salts, hydrates and solvates thereof, and wherein the neurodegenerative disease is selected from the group consisting of Alzheimer's disease, Huntington's disease, and Prion disorders.
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