G-protein-coupled receptor regulators and methods of use thereof
US-2024417378-A1 · Dec 19, 2024 · US
US10159667B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10159667-B2 |
| Application number | US-201414392160-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 17, 2014 |
| Priority date | Jun 26, 2013 |
| Publication date | Dec 25, 2018 |
| Grant date | Dec 25, 2018 |
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.
The present invention relates to a composition for preventing or treating renal diseases. The composition of the present invention improves lipid metabolism, prevents histological damage including renal fibrosis, alleviates microalbuminuria, and maintains nephrons of renal glomeruli. Therefore, the composition is useful for treating renal diseases.
Opening claim text (preview).
The invention claimed is: 1. A method of treating a renal disease in a subject who does not have diabetes, comprising: administering to the subject who has the renal disease who does not have diabetes a pharmaceutical composition comprising a therapeutically effective amount of a compound of Formula 1: or a pharmaceutically acceptable salt thereof, wherein: X is OR 1 and R 1 is tert-butyl; and the renal disease is a glomerulonephritis. 2. The method of claim 1 , wherein the pharmaceutically acceptable salt is selected from the group consisting of acetic acid, benzenesulfonic acid, benzoic acid, camphorsulfonic acid, citric acid, ethanesulfonic acid, fumaric acid, gluconic acid, glutamic acid, hydrobromic acid, hydrochloric acid, isethionic acid, lactic acid, maleic acid, malic acid, mandelic acid, methanesulfonic acid, mucic acid, nitric acid, pamoic acid, pantothenic acid, phosphoric acid, succinic acid, sulfuric acid, tartaric acid, p-toluenesulfonic acid and adipic acid. 3. The method of claim 1 , wherein the pharmaceutical composition further comprises an angiotensin converting enzyme inhibitor or an angiotensin II receptor blocker, wherein: the angiotensin converting enzyme inhibitor is selected from the group consisting of captopril, enalapril, benazepril, imidapril, lisinopril, prinopril, ramipril, moexipril, fosinopril and quinapril; and the angiotensin II receptor blocker is selected from the group consisting of candesartan, eprosartan, irbesartan, losartan, telmisartan and valsartan.
having six-membered rings with two {or more} nitrogen atoms as the only ring heteroatoms, e.g. piperazine {or tetrazines}(A61K31/48 takes precedence {; with three nitrogen atoms A61K31/53}) · CPC title
Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title
Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00 · CPC title
of the kidneys · CPC title
Non-condensed pyrazines · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.