C-substituted, 1H-azoles for amphoteric, solvent-less proton conductivity
US-9217062-B2 · Dec 22, 2015 · US
US9321740B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9321740-B2 |
| Application number | US-201213981502-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 26, 2012 |
| Priority date | Jan 26, 2011 |
| Publication date | Apr 26, 2016 |
| Grant date | Apr 26, 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.
Described herein are tetrazole compounds and their use in treating medical disorders, such as obesity. Pharmaceutical compositions and methods of making various tetrazole compounds are provided. The compounds are contemplated to have activity against methionyl aminopeptidase 2.
Opening claim text (preview).
What is claimed is: 1. The compounds N-[1-(1H-tetrazol-5-yl)-5,6,7,8-tetrahydronaphthalen-2-yl]-benzenesulfonamide, N-[3-cyclopropyl-2-(1H-tetrazol-5-yl)-phenyl]-benzenesulfonamide, N-[3-methoxy-2-(1H-tetrazol-5-yl)-phenyl]-benzenesulfonamide, N-[3-methyl-2-(1H-tetrazol-5-yl)-phenyl]-benzenesulfonamide, N-[3-bromo-2-(1H-tetrazol-5-yl)-phenyl]-benzenesulfonamide, and pharmaceutically acceptable salts thereof. 2. A pharmaceutical composition comprising a compound of claim 1 , and a pharmaceutically acceptable carrier. 3. The composition of claim 2 , wherein the composition is formulated as a unit dose. 4. The composition of claim 2 , wherein the composition is formulated for oral administration. 5. The composition of claim 2 , wherein the composition is formulated for intravenous or subcutaneous administration. 6. A method of inducing weight loss in a patient in need thereof, comprising administering to said patient a pharmaceutically effective amount of a compound of claim 1 . 7. A method of treating and/or controlling obesity, comprising administering to a patient in need thereof an effective amount of a compound of claim 1 . 8. The method of claim 7 , wherein the patient is a human. 9. The method of claim 7 , wherein the patient has a body mass index greater than or equal to about 30 kg/m 2 before the administration. 10. The method of claim 7 , wherein the compound is administered orally or subcutaneously.
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
Anorexiants; Antiobesity agents · CPC title
Five-membered rings · CPC title
having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole · CPC title
with nitrogen atoms directly attached to the ring carbon atom · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.