US2015299136A1PendingUtilityA1
Lxr modulators
Est. expiryMay 28, 2029(~2.8 yrs left)· nominal 20-yr term from priority
Inventors:Brett B. BuschWilliam C. Stevens, Jr.Ellen K. KickHaiying ZhangVenkataiah BolluRichard MartinRaju Mohan
A61P 37/00A61P 3/10A61P 5/50A61P 9/10A61P 3/08A61P 35/00A61P 43/00A61P 5/48A61P 3/06A61P 9/00A61P 27/00A61P 25/00A61P 3/04A61P 27/02A61P 25/28A61P 3/00A61P 29/00A61P 17/06A61P 19/02A61P 17/00A61P 17/16A61K 31/4164C07D 233/64A61K 31/415C07C 2601/14
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Claims
Abstract
Compounds, pharmaceutically acceptable salts, isomers, or prodrugs thereof, of the invention are disclosed, which are useful as modulators of the activity of liver X receptors (LXR). Pharmaceutical compositions containing the compounds and methods of using the compounds are also disclosed.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A compound selected from the group consisting of 2-(1-(3-chloro-3′-fluoro-4′-(hydroxymethyl)-5′-(methylsulfonyl)biphenyl-4-yl)-2-(2-(2-fluorophenyl)propan-2-yl)-1H-imidazol-4-yl)propan-2-ol and 2-(2-(2-(2-chloro-6-fluorophenyl)propan-2-yl)-1-(3′-fluoro-4′-(hydroxymethyl)-3-methyl-5′-(methylsulfonyl)biphenyl-4-yl)-1H-imidazol-4-yl)propan-2-ol, or isotope, or a pharmaceutically acceptable salt thereof.
2 . The compound of claim 1 , which is 2-(1-(3-chloro-3′-fluoro-4′-(hydroxymethyl)-5′-(methylsulfonyl)biphenyl-4-yl)-2-(2-(2-fluorophenyl)propan-2-yl)-1H-imidazol-4-yl)propan-2-ol, or isotope, or a pharmaceutically acceptable salt thereof.
3 . The compound of claim 1 , which is 2-(2-(2-(2-chloro-6-fluorophenyl)propan-2-yl)-1-(3′-fluoro-4′-(hydroxymethyl)-3-methyl-5′-(methylsulfonyl)biphenyl-4-yl)-1H-imidazol-4-yl)propan-2-ol, or isotope, or a pharmaceutically acceptable salt thereof.
4 . A pharmaceutical composition comprising a compound of claim 1 , or isotope, or a pharmaceutically acceptable salt thereof, and one or more pharmaceutically acceptable carriers.
5 . A method of treating a disease or disorder comprising administering to a subject in need thereof a therapeutically effective amount of a compound of claim 1 , or isotope, or a pharmaceutically acceptable salt thereof, wherein the disease or disorder is insulin resistance, osteoarthritis, stroke, hyperglycemia, psoriasis, age and UV exposure-related skin wrinkling, diabetes, cancer, Alzheimer's disease, inflammation, immunological disorders, lipid disorders, obesity, macular degeneration, conditions characterized by a perturbed epidermal barrier function, conditions of disturbed differentiation or excess proliferation of the epidermis or mucous membrane, or cardiovascular disorders.
6 . The method of claim 5 , wherein the disease or disorder is a cardiovascular disorder, a lipid disorder, diabetes, or Alzheimer's disease.
7 . The method of claim 6 , wherein the disease or disorder is a cardiovascular disorder.
8 . The method of claim 7 , wherein said cardiovascular disorder is atherosclerosis.
9 . The method of claim 6 , wherein the disease or disorder is a lipid disorder.
10 . The method of claim 9 , wherein said lipid disorder is dyslipidemia.
11 . The method of claim 5 wherein the disease or disorder is diabetes.
12 . The method of claim 5 wherein the disease or disorder is Alzheimer's disease.Join the waitlist — get patent alerts
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