Hydantoins that modulate BACE-mediated APP processing

Patent metadata

Field	Value
Publication number	US-10766867-B2
Application number	US-201715833862-A
Country	US
Kind code	B2
Filing date	Dec 6, 2017
Priority date	Feb 12, 2013
Publication date	Sep 8, 2020
Grant date	Sep 8, 2020

Abstract

In certain embodiments hydantoin compounds are provided herein that are effective to inhibit BACE activity against APP. Without being bound to a particular theory, it is believed the activity of the hydantoins identified herein appears to be associated with binding to BACE and/or to APP particularly when these moieties form a BACE/APP complex. Accordingly, it is believed the compounds described herein represent a new class of compounds designated herein as APP-Binding-BACE Inhibitors (ABBIs) and provide a new mechanism to modulate APP processing. The hydantoins described herein appear to show improved brain permeability and functional BACE inhibition.

First claim

What is claimed is:

1. A method of ameliorating one or more symptoms of a pre-Alzheimer's condition and/or cognitive dysfunction, or delaying the progression of a pre-Alzheimer's condition or cognitive dysfunction to Alzheimer's disease, said method comprising:
administering to a subject in need thereof a hydantoin in an amount sufficient to ameliorate one or more symptoms of a pre-Alzheimer's cognitive dysfunction, and/or to delay the progression of a pre-Alzheimer's cognitive dysfunction to Alzheimer's disease, wherein said hydantoin is a compound having a formula selected from the group consisting of

or a pharmaceutically acceptable salt thereof.

2. The method of claim 1 , wherein said method is a method of delaying the progression of a pre-Alzheimer's cognitive dysfunction to Alzheimer's disease.

3. The method of claim 1 , wherein:
said administration produces a reduction in the CSF of levels of one or more components selected from the group consisting of Aβ42, sAPPβ, total-Tau (tTau), phospho-Tau (pTau), APPneo, soluble Aβ40, pTau/Aβ42 ratio and tTau/Aβ42 ratio, and/or an increase in the CSF of levels of one or more components selected from the group consisting of Aβ42/Aβ40 ratio, Aβ42/Aβ38 ratio, sAPPα, sAPPβ/sAPPβ ratio, sAPPα/Aβ40 ratio, and sAPPα/Aβ42 ratio; and/or
said administration produces a reduction of the plaque load in the brain of the subject; and/or
said administration produces a reduction in the rate of plaque formation in the brain of the subject; and/or
said administration produces an improvement in the cognitive abilities of the subject; and/or
said administration produces an improvement in, a stabilization of, or a reduction in the rate of decline of the clinical dementia rating (CDR) of the subject.

4. The method of claim 1 , wherein said hydantoin is a compound having a formula:

or a pharmaceutically acceptable salt thereof.

5. The method of claim 4 , wherein said method is a method of delaying the transition from a cognitively asymptomatic pre-Alzheimer's condition to a pre-Alzheimer's cognitive dysfunction.

6. The method of claim 4 , wherein said method is a method of delaying the onset of a pre-Alzheimer's cognitive dysfunction.

7. The method of claim 4 , wherein said method is a method of delaying the progression of a pre-Alzheimer's cognitive dysfunction to Alzheimer's disease.

8. A method of ameliorating one or more symptoms of Alzheimer's disease, and/or reversing Alzheimer's disease, and/or reducing the rate of progression of Alzheimer's disease, said method comprising:
administering to a subject in need thereof a hydantoin in an amount sufficient to ameliorate one or more symptoms of Alzheimer's disease, and/or to reverse Alzheimer's disease, and/or to reduce the rate of progression of Alzheimer's disease, wherein said hydantoin is a compound having a formula selected from the group consisting of:

or a pharmaceutically acceptable salt thereof.

9. The method of claim 8 , wherein:
said subject is diagnosed with early stage Alzheimer's disease; or
said subject is diagnosed with mid-stage Alzheimer's disease; or
said subject is diagnosed with late-stage Alzheimer's disease.

10. The method of claim 8 , wherein:
said administering ameliorates one or more symptoms of Alzheimer's disease; and/or
said administering reduces the rate of progression of Alzheimer's disease; and/or
said administering results in a reduction in the CSF of levels of one or more components selected from the group consisting of Aβ42, sAPPβ, total-Tau (tTau), phospho-Tau (pTau), APPneo, soluble Aβ40, pTau/Aβ42 ratio and tTau/Aβ42 ratio, and/or an increase in the CSF of levels of one or more components selected from the group consisting of Aβ42/Aβ40 ratio, Aβ42/Aβ38 ratio, sAPPα, sAPPα/sAPPβ ratio, sAPPα/Aβ40 ratio, and sAPPα/Aβ42 ratio; and/or
said administration produces a reduction of the plaque load in the brain of the subject; and/or
said administration produces a reduction in the rate of plaque formation in the brain of the subject; and/or
said administration produces an improvement in the cognitive abilities of the subject; and/or
said administration produces an improvement in, a stabilization of, or a reduction in the rate of decline of the clinical dementia rating (CDR) of the subject; and/or
said administration produces a perceived improvement in quality of life by the subject; and/or
said administering results in reduced cerebral amyloidosis and/or downstream neurodegeneration.

11. The method of claim 8 , wherein:
said subject shows a clinical dementia rating indicative of Alzheimer's disease; and/or
said subject has a familial risk for having Alzheimer's disease; and/or
said subject has a familial Alzheimer's disease (FAD) mutation.

12. The method of claim 8 , wherein said hydantoin is a compound having a formula:

or a pharmaceutically acceptable salt thereof.

13. A method of slowing the progression, stopping, or reversing age-related macular degeneration (AMD) in a mammal, said method comprising administering to said mammal a hydantoin in an amount sufficient to slow the progression, stop, or reverse age-related macular degeneration in said mammal, wherein said hydantoin is a compound having a formula selected from the group consisting of:

or a pharmaceutically acceptable salt thereof.

14. The method of claim 13 , wherein said hydantoin is a compound having a formula:

or a pharmaceutically acceptable salt thereof.

15. A method for delaying the onset of a disease or a disorder, or reversing or retarding the progress of the disease or the disorder, or reducing the severity of the disease or the disorder, or alleviating one or more symptoms of the disease or the disorder, wherein the disease or the disorder is associated with BACE activity and characterized by the production of amyloid deposits and/or neurofibrillary tangles in a subject, wherein said method comprises providing to said subject a therapeutically effective amount of a hydantoin, wherein said hydantoin is a compound having a formula selected from the group consisting of:

Assignees

• Buck Inst Res Aging

Inventors

• John Varghese
• Bredesen Dale E

Classifications

• C07D403/10

  linked by a carbon chain containing aromatic rings · CPC title

• C07D401/10

  linked by a carbon chain containing aromatic rings · CPC title

• C07D233/88 Primary

  Nitrogen atoms, e.g. allantoin · CPC title

• C07D233/76 Primary

  with substituted hydrocarbon radicals attached to the third ring carbon atom · CPC title

• C07D233/70 Primary

  One oxygen atom · CPC title