Abstract: The present invention relates to benzimidazolinylpiperidine derivatives useful as ligands for CGRP (Calcitonin Gene-Related Peptide) receptors, their use in therapy, pharmaceutical compositions comprising them and methods of treatment using them.
Type:
Grant
Filed:
May 30, 2001
Date of Patent:
April 22, 2003
Assignees:
Merck Sharpe & Dohme Ltd., Merck & Co, Inc.
Inventors:
Arthur A. Patchett, Raymond George Hill, Lihu Yang
Abstract: This invention encompasses a process for making a compound of Formula A
These compounds are intermediates useful in the preparation of certain non-steroidal anti-inflammnatory agents.
Type:
Grant
Filed:
January 17, 2002
Date of Patent:
December 17, 2002
Assignee:
Merck & Co., Inc.
Inventors:
Cheng Yi Chen, Weirong Chen, Paul O'Shea, Lushi Tan, Richard Tillyer, Feng Xu, Philippe Dagneau
Abstract: A COX-2 selective inhibiting drug is disclosed as useful in treating or preventing prostate cancer. The compound is used alone or in combination with other drugs.
Type:
Grant
Filed:
January 26, 2001
Date of Patent:
November 26, 2002
Assignee:
Merck & Co., Inc.
Inventors:
Joanne Waldstreicher, Briggs W. Morrison
Abstract: Compounds represented by formula I:
as well as pharmaceutically acceptable salts, esters, N-oxides and hydrates thereof are disclosed. Pharmaceutical compositions and methods of use are also included. The compounds are active against the caspase-3 enzyme, and thus are useful to treat fin caspase-3 mediated diseases and conditions.
Type:
Grant
Filed:
July 19, 2000
Date of Patent:
September 3, 2002
Assignee:
Merck Frosst Canada & Co.
Inventors:
Yongxin Han, Andre Giroux, Robert Zamboni, Daniel J. McKay, Christopher I. Bayly, Erich L. Grimm, John Colucci
Abstract: Polymorphic, amorphous and hydrated forms of the title compound having the following structure:
are disclosed. The compound is a potent and selective cyclooxygenase-2 (COX-2) inhibitor.
Abstract: Compounds represented by formula I:
as well as pharmaceutically acceptable salts and hydrates thereof are disclosed as useful for treating or preventing diseases and conditions mediated by PDE-IV.
Pharmaceutical compositions and methods of treatment are also included.
Type:
Grant
Filed:
March 1, 2001
Date of Patent:
August 20, 2002
Assignee:
Merck Frosst Canada & Co.
Inventors:
Marc Labelle, Claudio Sturino, Nicolas Lachance, Dwight Macdonald
Abstract: Immunoregulatory compounds are disclosed of the formula:
as well as the pharmaceutically acceptable salts and hydrates thereof, are disclosed. The compounds are useful for treating immune mediated diseases and conditions, such as bone marrow, organ and tissue transplant rejection.
Pharmaceutical compositions and methods of use are included.
Type:
Grant
Filed:
August 30, 2001
Date of Patent:
August 20, 2002
Assignee:
Merck & Co., Inc.
Inventors:
Suzanne Mandala, James Bergstrom, Richard Hajdu, Hugh Rosen, William Parsons, Deborah J. Card, Malcolm Maccoss, Rupprecht Kathleen
Abstract: Disclosed herein are compounds of Formula I
and pharmaceutically acceptable salts thereof which have been found useful in the treatment of nitric oxide synthase mediated diseases and disorders, including neurodegenerative disorders, disorders of gastrointestinal motility and inflammation.
Type:
Grant
Filed:
January 4, 2000
Date of Patent:
April 16, 2002
Assignee:
Merck & Co., Inc.
Inventors:
Charles G. Caldwell, Malcolm Maccoss, William K. Hagmann, Shrenik K. Shah, Kothandaraman Shankaran, Karla L. Furman
Abstract: This invention encompasses the novel compounds of formula A, which are useful in the treatment of prostaglandin mediated diseases,
or a pharmaceutically acceptable salt, hydrate or ester thereof. The invention also encompasses pharmaceutical compositions and methods for treatment of prostaglandin mediated diseases.
Type:
Grant
Filed:
September 14, 2000
Date of Patent:
April 9, 2002
Assignee:
Merck Frosst Canada & Co.
Inventors:
Patrick Lacombe, Marc Labelle, Rejean Ruel
Abstract: This invention encompasses the novel compounds of formula A, which are useful in the treatment of prostaglandin mediated diseases,
or a pharmaceutically acceptable salt, hydrate or ester thereof. The invention also encompasses certain pharmaceutical compositions and methods for treatment of prostaglandin mediated diseases comprising the use of compounds of formula A.
Type:
Grant
Filed:
September 14, 2000
Date of Patent:
April 9, 2002
Assignee:
Merck Frosst Canada & Co.
Inventors:
Patrick Lacombe, Marc Labelle, Rejean Ruel
Abstract: Disclosed are novel chromophore containing compounds of Formula I and their use in determining interleukin-1&bgr; convertase (ICE) activity. ICE has been implicated in inflammatory or immune-based diseases of the lung and airways; central nervous system and surrounding membranes; the eyes and ears; joints, bones, and connective tissues; cardiovascular system including the pericardium; the gastrointestinal and urogenital systems; the skin and mucosal membranes.
Type:
Grant
Filed:
December 17, 1991
Date of Patent:
February 19, 2002
Assignee:
Merck & Co., Inc.
Inventors:
Kevin T. Chapman, Malcolm Maccoss, Richard A. Mumford, Nancy A. Thornberry, Jeffrey R. Weidner, William K. Hagmann
Abstract: The present invention relates to biphenylene lactams of Formula II which are ligands at the prostaglandin receptors, as well as a method for treating prostaglandin mediated diseases comprising administration to a patient in need of such a treatment of a non-toxic therapeutically effective amount of compound of Formula II, and the like.
Type:
Grant
Filed:
October 1, 1999
Date of Patent:
August 21, 2001
Assignee:
Merck Frosst Canada & Co.
Inventors:
Joseph G. Atkinson, Marc Labelle, Patrick Lacombe, Rejean Ruel
Abstract: Compounds of formula I:
as well as pharmaceutically acceptable salts, hydrates and esters thereof, are disclosed.
The compounds are useful for treating or preventing prostaglandin mediated diseases. Pharmaceutical compositions containing such compounds and methods of treatment are also included.
Type:
Grant
Filed:
March 10, 1999
Date of Patent:
June 5, 2001
Assignee:
Merck Frosst Canada & Co.
Inventors:
Yves Gareau, Marc LaBelle, Helene Juteau, Michel Gallant, Nicolas LaChance, Michel Belley
Abstract: This invention encompasses a novel process for synthesizing the compound represented by formula I:
These compounds are useful as non-steroidal anti-inflammatory agents.
Type:
Grant
Filed:
September 13, 2000
Date of Patent:
May 15, 2001
Assignee:
Merck Frosst Canada & Co.
Inventors:
Paul O'Shea, Xin Wang, Richard D. Tillyer, Sophie-Dorothee Clas, Chad Dalton
Abstract: Compounds represented by formula I:
as well as pharmaceutically acceptable salts, esters and hydrates thereof are disclosed along with pharmaceutical compositions and methods of treatment. The compounds are useful as inhibitors of caspase-3, which is implicated in modulating apoptosis.
Type:
Grant
Filed:
March 16, 2000
Date of Patent:
May 1, 2001
Assignee:
Merk Frosst Canada & Co.
Inventors:
Yongxin Han, Andre Giroux, Erich Grimm, Renee Aspiotis, Sebastien Francoeur, Robert Zamboni, Petpiboon Prasit, Christopher Bayly, Dan McKay, Cameron Black
Abstract: The invention encompasses the novel compound of Formula (I) as well as a method of treating cyclooxygenase-2 mediated diseases comprising administration to a patient in need of such treatment of a non-toxic therapeutically effective amount of a compound of Formula (I). The invention also encompasses certain pharmaceutical compositions for treatment of cyclooxygenase-2 mediated diseases comprising compounds of Formula (I).
Type:
Grant
Filed:
June 12, 1997
Date of Patent:
April 24, 2001
Assignee:
Merck Frosst Canada & Co.
Inventors:
Cameron Black, Erich Grimm, Serge Leger, Petpiboon Prasit, Zhaoyin Wang