Abstract: This invention relates to potent potassium channel blocker compounds of structural Formula I or a formulation thereof for the treatment of glaucoma and other conditions which leads to elevated intraoccular pressure in the eye of a patient. This invention also relates to the use of such compounds to provide a neuroprotective effect to the eye of mammalian species, particularly humans.
Type:
Grant
Filed:
August 31, 2004
Date of Patent:
February 24, 2009
Assignee:
Merck & Co. Inc.
Inventors:
Meng Hsin Chen, James B. Doherty, Luping Liu, Swaminathan Natarajan, Robert M. Tynebor
Abstract: The invention relates to processes for preparing compounds having the formula, and crystalline forms thereof, wherein Ar is aryl or heteroaryl, L is an optional alkylene linker, and R2, R3, R4, and R5, are as defined in the specification herein, which compounds are useful as kinase inhibitors, in particular, inhibitors of protein tyrosine kinase and p38 kinase.
Type:
Grant
Filed:
July 29, 2005
Date of Patent:
February 17, 2009
Assignee:
Bristol-Myers Squibb Company
Inventors:
Jean Lajeunesse, John D. DiMarco, Michael Galella, Ramakrishnan Chidambaram
Abstract: Provided is an efficient method for the preparation of 3-aryloxy-3-arylpropylamines, their optical stereoisomers, and pharmaceutically acceptable salts thereof. The process allows for the isolation of 3-aryloxy-3-arylpropylamines in high yield and purity. The present invention further relates to a process for producing fluoxetine, tomoxetine, norfluoxetine, duloxetine, nisoxetine, and their optically enriched (R)- and (S)-enantiomers.
Type:
Grant
Filed:
July 8, 2005
Date of Patent:
February 3, 2009
Assignee:
Apotex Pharmachem Inc.
Inventors:
Zhi-Xian Wang, Mohammed Abdul Raheem, Gamini Weeratunga, Bhaskar Reddy Guntoori
Abstract: The invention relates to compounds of formula (I): and pharmaceutically acceptable salts and pharmaceutically acceptable esters thereof, wherein R1, R2, R3, R4, R5, R6, A, m, n and p are defined as in claim 1. These compounds can be used as pharmaceutical compositions for the treatment of, for example, diabetes.
Abstract: Novel inhibitors of cathepsin S, K, B, and L, the pharmaceutically acceptable salts and N-oxides thereof, their uses as therapeutic agents and the methods of their making.
Type:
Grant
Filed:
April 24, 2006
Date of Patent:
January 27, 2009
Assignee:
Aventis Pharmaceuticals Inc.
Inventors:
Sukanthini Thurairatnam, David John Aldous, Vincent Leroy, Andreas Paul Timm
Abstract: Compounds of the invention, such as compounds of formula (I): where n, m, A, B, R1, R2, R3, R4 and R5 are defined herein, are useful as modulators of the activity of liver X receptors. Pharmaceutical compositions containing the compounds and methods of using the compounds are also disclosed.
Type:
Grant
Filed:
July 24, 2004
Date of Patent:
January 27, 2009
Assignee:
X-Ceptor Therapeutics, Inc.
Inventors:
Christopher D Bayne, Alan T Johnson, Shao-Po Lu, Raju Mohan, Michael C Nyman, Edwin J Schweiger, William C Stevens, Jr., Haixia Wang, Yinong Xie
Abstract: Heterocyclic arylsulfonamidobenzylic compounds are provided which are useful in treating lipid disorders, metabolic disorders and cell-proliferative diseases.
Type:
Grant
Filed:
August 8, 2006
Date of Patent:
January 6, 2009
Assignee:
Amgen Inc.
Inventors:
Xian Yun Jiao, Frank Kayser, David J. Kopecky, Sharon McKendry, Derek E. Piper, Andrew K. Shiau
Abstract: The present invention relates to compounds of the Formula wherein R1, R3, R4, R5, R6, R7 and R8 are as defined. Compounds of the Formula I have activity inhibiting production of A?-peptide. The invention also relates to pharmaceutical compositions and methods of treating disorders and diseases, for example, neurodegenerative and/or neurological disorders, e.g., Alzheimer's disease, in a mammal comprising compounds of the Formula I.