IP Library Granted Patent US 9,370,504
Granted Patent B2
US 9,370,504 · App. 13/057,401 · Granted Jun 21, 2016

Pharmaceutical composition containing 1,2-dithiolthione derivative for preventing or treating disease caused by overexpression of LXR-α

Inventors: Sang Geon Kim (Seoul, KR); Sung Hwan Ki (Seoul, KR); Seong Hwan Hwang (Ulsan, KR)
Assignee: SNU R&DB FOUNDATION
A61K31/385
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Quick Facts
Patent No.
US 9,370,504
App. No.
13/057,401
Granted
Jun 21, 2016
Kind
B2
Abstract

Provided is a pharmaceutical composition that contains a 1,2-dithiolthionederivative, and is effective to prevent and treat a disease caused by overactivity of a liver X receptorα (LXRα) or a sterol response element binding protein (SREBP-1). Specifically, the pharmaceutical composition includes 1,2-dithiolthione derivatives such as 4-methyl-5-(2-pyrazinyl)-1,2-dithiol-3-thione, 3-methyl-1,2-dithiol-3-thione, or 5-(6-methoxypyrazinyl)-4-methyl-1,2-dithiol-3-thione. The pharmaceutical composition is effective for preventing and treating hypertension caused by renin, aldosteronism, adrenoleukodystrophy, glomerulosclerosis, proteinuria, nephropathy, liver steatosis, hypertriglyceridemia or hyperreninemia.

Claims (8)

1. A method for treating liver steatosis, comprising administering an effective amount of a compound selected from the group consisting of the following compounds, or a pharmaceutically acceptable salt thereof, to a subject in need thereof:

2. A method for treating liver steatosis, comprising administering an effective amount of 4-methyl-5-(2-pyrazinyl)-1,2-dithiol-3-thione, or a pharmaceutically acceptable salt thereof, to a subject in need thereof.

3. The method for treating liver steatosis according to claim 1 , wherein the compound or the pharmaceutically acceptable salt thereof is administered at a dose of 1-500 mg in one day.

4. The method for treating liver steatosis according to claim 1 , wherein the compound or the pharmaceutically acceptable salt thereof is administered at a dose of 60-120 mg in one day.

5. The method for treating liver steatosis according to claim 2 , wherein the compound or the pharmaceutically acceptable salt thereof is administered at a dose of 1-500 mg in one day.

6. The method for treating liver steatosis according to claim 2 , wherein the compound or the pharmaceutically acceptable salt thereof is administered at a dose of 60-120 mg in one day.

7. The method for treating liver steatosis according to claim 3 , wherein the compound or the pharmaceutically acceptable salt thereof is administered at a dose of 30-200 mg in one day.

8. The method for treating liver steatosis according to claim 5 , wherein the compound or the pharmaceutically acceptable salt thereof is administered at a dose of 30-200 mg in one day.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2011
From: KIM, SANG GEON; KI, SUNG HWAN; HWANG, SEONG HWAN
To: SNU R&DB FOUNDATION
Reel/Frame 025751/0802 →
Priority Claims (1)
KR 10-2008-0075994 · Aug 4, 2008 · national
Continuity (1)
Related Publication 20110152524A1 · Jun 23, 2011