Novel methods of treating hearing loss
US-2024390323-A1 · Nov 28, 2024 · US
US9259412B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9259412-B2 |
| Application number | US-201214354332-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 24, 2012 |
| Priority date | Oct 25, 2011 |
| Publication date | Feb 16, 2016 |
| Grant date | Feb 16, 2016 |
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The present invention relates to modafinil or derivatives thereof as a medicine for the treatment of vascular diseases or KCa3.1 channel (Ca activated K channel) mediated diseases and a novel use of the same. More specifically, the present invention relates to a pharmaceutical composition for the prevention or treatment of vascular diseases or KCa3.1 channel-mediated diseases comprising modafinil or a derivative of modafinil, or pharmaceutically acceptable salts thereof which relax blood vessels and inhibit KCa3.1 channel currents by increasing intracellular cAMP, a method for treating vascular diseases or KCa3.1 channel-mediated diseases using the composition and a health functional food composition for the prevention or improvement of vascular diseases or the KCa3.1 channel-mediated diseases comprising modafinil or a modafinil derivative compound, or sitologically acceptable salts thereof.
Opening claim text (preview).
The invention claimed is: 1. A method of treating KCa3.1 channel-mediated disease comprising administering the composition comprising modafinil or derivatives of modafinil having below Chemical Formulas 2 to 5, or pharmaceutically acceptable salts thereof to an individual in need thereof, wherein the KCa3.1 channel-mediated disease is any one selected from the group consisting of sickle cell anemia; immune diseases comprising acute immune response or auto-immune diseases; vascular diseases comprising hypertension, ischemic coronary artery disease, arteriosclerosis, peripheral arterial occlusion, restenosis, atherosclerosis or pulmonary hypertension; cancers comprising prostate cancer or pancreatic cancer; and secretory diarrhea 2. The method of claim 1 , the composition further comprising a pharmaceutically acceptable carrier. 3. The method of claim 1 , wherein the composition relaxes vascular smooth muscle by increasing intracellular cAMP concentration. 4. The method of claim 1 , wherein the composition inhibits KCa3.1 channel by increasing intracellular cAMP concentration.
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