G-protein-coupled receptor regulators and methods of use thereof
US-2024417378-A1 · Dec 19, 2024 · US
US9469653B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9469653-B2 |
| Application number | US-201414164616-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 27, 2014 |
| Priority date | Aug 18, 2011 |
| Publication date | Oct 18, 2016 |
| Grant date | Oct 18, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A pharmaceutical composition for preventing or treating a degenerative brain disease, and a method of screening a material for preventing or treating a degenerative brain disease. The method may effectively screen a prophylactic or therapeutic candidate material for preventing or treating a degenerative brain disease. A variety of degenerative brain diseases may be effectively prevented or treated using the pharmaceutical composition including a screened material for preventing or treating a degenerative brain disease.
Opening claim text (preview).
What is claimed is: 1. A method for treating a degenerative brain disease, the method comprising administering to a subject in need thereof an effective amount of a pharmaceutical composition comprising a compound represented by Formula 1 below, a pharmaceutically acceptable salt, an isomer, a solvate, a hydrate, or a combination thereof, wherein, in Formula 1 above, R 1 and R 2 are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a carboxyl group, a hydroxyl group, a substituted or unsubstituted C 1 -C 12 alkyl group, a substituted or unsubstituted C 2 -C 12 alkenyl group, a substituted or unsubstituted C 2 -C 12 alkynyl group, a substituted or unsubstituted C 3 -C 15 cycloalkyl group, a substituted or unsubstituted C 3 -C 40 heterocycloalkyl group, (a substituted or unsubstituted C 6 -C 20 aryl) C 1 -C 12 alkyl group, a substituted or unsubstituted C 1 -C 12 alkoxy group, a substituted or unsubstituted C 6 -C 20 arylamine group, a substituted or unsubstituted C 6 -C 30 diarylamine group, a substituted or unsubstituted C 6 -C 20 aryloxy group, a substituted or unsubstituted C 6 -C 20 aryl group, or a substituted or unsubstituted C 5 -C 20 heteroaryl group; and X is —O—, —S—, or —N(H)—, and the compound represented by Formula 1 is at least one of N-cyclohexyl-2-phenyloxazolo[5,4-b]pyridine-5-amine, 2-phenyl-5-(pyrrolidine-1-yl)thiazolo[5,4-b]pyridine, 2-(2-chlorophenyl)-5-(pyrrolidine-1-yl)oxazolo[5,4-b]pyridine, 2-(3-chlorophenyl)-5-(pyrrolidine-1-yl)oxazolo[5,4-b]pyridine, 2-(4-fluorophenyl)-5-(pyrrolidine-1-yl)oxazolo[5,4-b]pyridine, 2-phenyl-5-(piperidine-1-yl)oxazolo[5,4-b]pyridine, 2-phenyl-5-(piperidine-1-yl)thiazolo[5,4-b]pyridine, 2-(2-chlorophenyl)-5-(piperidine-1-yl)oxazolo[5,4-b]pyridine, 2-(3-fluorophenyl)-5-(piperidine-1-yl)oxazolo[5,4-b]pyridine, 2-(3-chlorophenyl)-5-(piperidine-1-yl)oxazolo[5,4-b]pyridine, 3-(5-(piperidine-1-yl)oxazolo[5,4-b]pyridine-2-yl)benzonitrile, 2-(4-fluorophenyl)-5-(piperidine-1-yl)oxazolo[5,4-b]pyridine, 2-(4-bromophenyl)-5-(piperidine-1-yl)oxazolo[5,4-b]pyridine, 2-(3-chlorophenyl)-N-methyloxazolo[5,4-b]pyridine-5-amine, or 2-(4-chlorophenyl)-N-methyloxazolo[5,4-b]pyridine-5-amine. 2. The method of claim 1 , wherein the degenerative brain disease is selected from the group consisting of Alzheimer's disease, mild cognitive impairment, vascular dementia, frontotemporal dementia, Louis corpuscle dementia, Creutzfeld-Jakob disease, traumatic head injuries, syphilis, acquired immune deficiency syndrome (AIDS), viral infection, brain abscess, brain tumor, dementia in metabolic disease, hypoxia, Parkinson's disease, Huntington's disease, Pick's disease, epilepsy, ischemia, stroke, attention deficit hyperactivity disorder (ADHD), schizophrenia, depression, manic-depression, and stress disorder.
Related publications grouped by family.
Answers are generated from the same data shown on this page.