GluN2C/D Subunit Selective Antagonists of the N-Methyl-D-Aspartate Receptor
US-2024294493-A1 · Sep 5, 2024 · US
US9901569B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9901569-B2 |
| Application number | US-201514924605-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 27, 2015 |
| Priority date | Oct 30, 2014 |
| Publication date | Feb 27, 2018 |
| Grant date | Feb 27, 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.
Compositions and methods for inhibiting Leishmaniasis using AIs are provided. Aspects provide compositions and methods for administering AIs alone or in combination with other compounds to infected hosts.
Opening claim text (preview).
What is claimed as new and desired to be protected by Letters Patent of the United States is: 1. A method of reducing the Leishman-Donovan units (LDU) of Leishmaniasis in a host, comprising: administering a daily dose of at least about 0.1 mg/kg of an autophagy inducer (AI) to the host wherein the AI is AR-12 (2-amino-N-(4-(5-(phenanthren-2-yl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)phenyl)acetamide) and is co-administered with a second compound, and the Leishman-Donovan units (LDU) of Leishmaniasis in the host of Leishmaniasis are reduced. 2. The method of claim 1 , wherein the Leishman-Donovan units (LDU) are reduced to less than about 47% of the untreated control. 3. The method of claim 1 , wherein the second compound is selected from the group consisting of sodium stibogluconate (SSG), amphotericin B, pentamidine isethionate, miltefosine, ketoconazole, itraconazole, and fluconazole. 4. The method of claim 3 , wherein the resulting Leishman-Donovan units (LDU) is less than about 1% of the untreated control. 5. A method of treating a host infected with Leishmaniasis, comprising: administering a daily dose of at least about 0.1 mg/kg of an autophagy inducer (AI) and a second compound to the host, wherein the AI is AR-12 (2-amino-N-(4-(5-(phenanthren-2-yl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)phenyl)acetamide). 6. The method of claim 5 , wherein the second compound is selected from the group consisting of sodium stibogluconate (SSG), amphotericin B, pentamidine isethionate, miltefosine, ketoconazole, itraconazole, and fluconazole.
Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title
1,2-Diazoles · 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
having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin {, digitoxin or digoxin} · CPC title
Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.