Methods of treating elevated plasma cholesterol
The present invention relates to compounds of Formula I, pharmaceutically acceptable salts, solvates or formulations thereof. Compounds of Formula I increase significantly low density lipoprotein receptor and are useful for preventing and treating of elevated cholesterol.
1. A method of lowering low-density lipoprotein (LDL)-cholesterol level in the bloodstream of a subject, the method comprising administering to the subject a LDL-lowering amount of 5-[(4-fluoro-phenylamino)-methyl]-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, 5-(4-fluoro-phenoxymethyl)-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, or 5-[2-(4-fluoro-phenyl)-ethyl]-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide
or
a pharmaceutically acceptable salt thereof.
2. The method of claim 1 , wherein the compound is 5-[(4-fluoro-phenylamino)-methyl]-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, or a pharmaceutically acceptable salt thereof.
3. The method of claim 1 , wherein the compound is 5-(4-fluoro-phenoxymethyl)-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, or a pharmaceutically acceptable salt thereof.
4. The method of claim 1 , wherein the compound is 5-[2-(4-fluoro-phenyl)-ethyl]-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, or a pharmaceutically acceptable salt thereof.
5. The method of claim 1 , wherein the subject has been diagnosed with atherosclerosis, hypercholesterolemia, hypertriglyceridemia, diabetic complications, dyslipidemia, hyperlipidemia, hypoalphalipoproteinemia, metabolic syndrome, stroke, vascular dementia, chronic kidney disease, coronary heart disease, coronary artery disease, retinopathy, inflammation, thrombosis, peripheral vascular disease or congestive heart failure.
6. A method of treating atherosclerosis, hypercholesterolemia, dyslipidemia, or hyperlipidemia the method comprising administering to a subject in need thereof, a therapeutically effective amount of 5-[(4-fluoro-phenylamino)-methyl]-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, 5-(4-fluoro-phenoxymethyl)-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, or 5-[2-(4-fluoro-phenyl)-ethyl]-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide;
or
a pharmaceutically acceptable salt thereof.
7. The method of claim 6 , wherein the compound is 5-[(4-fluoro-phenylamino)-methyl]-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, or a pharmaceutically acceptable salt thereof.
8. The method of claim 6 , wherein the compound is 5-(4-fluoro-phenoxymethyl)-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, or a pharmaceutically acceptable salt thereof.
9. The method of claim 6 , wherein the compound is 5-[2-(4-fluoro-phenyl)-ethyl]-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, or a pharmaceutically acceptable salt thereof.
10. The method of claim 1 , wherein a pharmaceutical composition comprising the compound or the salt is administered to the subject.
11. A method of inducing low density lipoprotein receptor (LDLR) expression in a cell, the method comprising contacting the cell with an effective amount of 5-[(4-fluoro-phenylamino)-methyl]-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, 5-(4-fluoro-phenoxymethyl)-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, or 5-[2-(4-fluoro-phenyl)-ethyl]-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide;
or
a pharmaceutically acceptable salt thereof.
12. A method of modulating LDLR mRNA activity in a cell, the method comprising contacting the cell with an effective amount of 5-[(4-fluoro-phenylamino)-methyl]-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, 5-(4-fluoro-phenoxymethyl)-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide, or 5-[2-(4-fluoro-phenyl)-ethyl]-3-hydroxy-4-hydroxymethyl-pyridine-2-carboxylic acid hydroxyamide;
or
a pharmaceutically acceptable salt thereof.
13. The method of claim 1 , further comprising administering a second cholesterol lowering agent to the subject.
14. The method of claim 13 , wherein the second cholesterol lowering agent is a cholesterol synthesis inhibitor.
15. The method of claim 14 , wherein the cholesterol synthesis inhibitor is a statin.
16. The method of claim 15 , wherein the statin is atorvastatin.