Abstract: This invention relates to muscarinic receptor antagonist compounds selected from the group of compounds represented by Formula I:
wherein the substituents are as defined in the specification; and their pharmaceutically acceptable salts, individual isomers or a racemic or non-racemic mixture; pharmaceutical compositions containing them; and methods for their use as therapeutic agents.
Type:
Grant
Filed:
February 1, 1999
Date of Patent:
November 20, 2001
Assignee:
Syntex (U.S.A.) LLC
Inventors:
Joan Marie Caroon, Robin Douglas Clark, Michael Patrick Dillon, Ralph New Harris, III, Sharathchandra Surendra Hegde, Clara Jeou Jen Lin, Hans Maag, David Bruce Repke
Abstract: The present invention relates to compounds of Formula (I)
that are p-38 MAP kinase inhibitors, pharmaceutical compositions containing them, methods for their use, and methods for preparing these compounds.
Type:
Grant
Filed:
October 16, 1998
Date of Patent:
November 13, 2001
Assignee:
Syntex (U.S.A.) LLC
Inventors:
Soan Cheng, David Michael Goldstein, Teresa Alejandra Trejo Martin, Eric Brian Sjogren
Abstract: The present invention relates to certain pyrazole derivatives of Formula (I):
that are p-38 MAP kinase inhibitors, pharmaceutical compositions containing them, methods for their use, and methods for preparing these compounds.
Type:
Grant
Filed:
September 22, 1999
Date of Patent:
November 13, 2001
Assignee:
Syntex (U.S.A.) LLC
Inventors:
David Michael Goldstein, Sharada Shenvi Labadie, David Mark Rotstein, Eric Brian Sjogren, Francisco Xavier Talamas
Abstract: The invention provides TCCV-1 or TCCV-2 from human, reagents related thereto including polynucleotides encoding TCCV-1 or TCCV-2, purified polypeptides, and specific antibodies. Methods of making and using these reagents, in particular, methods for screening compounds which modulate TCCV-1 or TCCV-2 activity are provided. Also provided are methods of diagnosis and kits.
Type:
Grant
Filed:
September 23, 1999
Date of Patent:
October 30, 2001
Assignee:
Syntex (U.S.A.) LLC
Inventors:
Paul Shartzer Dietrich, Joseph Gerard McGivern
Abstract: This invention provides methods of treating emphysema and other diseases associated with alveolar damage by treatment with an RAR&ggr; selective agonist. In another aspect, this invention provides methods of promoting tropoelastin gene expression and alveolar matrix repair by contacting the pulmonary intestitial fibroblast with an RAR agonist, preferably an RAR&ggr; selective agonist.
Abstract: Compounds selected from the group of compounds represented by Formula I:
as an individual isomer or as a racemic or non-racemic mixture of isomers, and their pharmaceutically acceptable salts and N-oxides thereof; are sodium channel blockers, and thus exhibit useful pharmacological properties, including utility for the treatment of neuropathic pain conditions.
Type:
Grant
Filed:
April 20, 2000
Date of Patent:
July 17, 2001
Assignee:
Syntex (U.S.A.) LLC
Inventors:
David Garrett Loughhead, Xiao-Fa Lin, Robert James Weikert, Lee Allen Flippin
Abstract: This invention relates to compounds which are generally alpha1A/B-receptor antagonists and which are represented by Formula I:
wherein the substituents are as defined in the specification; or pharmaceutically acceptable salts, hydrates, or N-oxides thereof. The invention further relates to pharmaceutical compositions containing such compounds, methods for their use as therapeutic agents, and a process for their preparation.
Abstract: This invention is directed to a process for the preparation of enteric coated pharmaceutical dosage forms. This invention is further directed to the aqueous enteric coating dispersions suitable for use in the process and the enteric coated pharmaceutical dosage forms prepared by the process.
Abstract: 5-Benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxamides of the formula
where R1 is alkyl and R2 is optionally substituted phenyl,
and the method for their preparation and their conversion to ketorolac and its pharmaceutically acceptable salts.
Type:
Grant
Filed:
December 13, 1999
Date of Patent:
March 6, 2001
Assignee:
Syntex (U.S.A.) LLC
Inventors:
Peter J. Harrington, Hiralal N. Khatri, George C. Schloemer
Abstract: Truncated forms of inhibitory kappa B protein (I&kgr;B-&agr;), nucleic acids encoding the truncates, expression and delivery vectors, and therapeutic and prophylatic uses thereof are provided.
Type:
Grant
Filed:
July 8, 1999
Date of Patent:
February 27, 2001
Assignee:
Syntex (U.S.A.) LLC
Inventors:
Paula Nanette Belloni, Gary Allen Peltz