Abstract: Benzo[de]isoquinoline-1,3-diones which are selective inhibitors of bacterial DNA gyrase and DNA topoisomerase useful in antibacterial agents are described as well as methods for their preparation and formulation. Novel intermediates useful in the preparation of the final products are also described.
Type:
Grant
Filed:
August 11, 2000
Date of Patent:
March 26, 2002
Assignee:
Warner-Lambert Company
Inventors:
Albert Kudzoi Amegadzie, Maureen Elizabeth Carey, John Michael Domagala, Liren Huang, Ronald George Micetich, Joseph Peter Sanchez, Rajeshwar Singh, Michael Andrew Stier, Arkadii Vaisburg
Abstract: The present invention provides novel N-type calcium channel blockers, compositions comprising them, and methods of their use. The compounds of the invention are useful in the treatment of stroke, cerebral ischemia, pain, epilepsy, and head trauma.
Abstract: Hydroxylated derivatives of cholesterol lowering agents inhibit the oxidation of lipoproteins, and are thus useful for preventing the progression of atherogenesis and resultant vascular diseases, including heart attacks.
Type:
Grant
Filed:
February 7, 2000
Date of Patent:
March 26, 2002
Assignee:
Warner-Lambert Company
Inventors:
Michael Aviram, Charles Larry Bisgaier, Roger Schofield Newton, Mira Rosenblat
Abstract: The invention relates to the use of trimebutine [2-dimethylamino-2-phenylbutyl-3,4,5-trimethoxy-benzoate hydrogen maleate] or its corresponding stereoisomers for the preparation of a medicament to prevent and/or treat arthritis, osteo-traumatic pain, and neuralgias.
Type:
Grant
Filed:
January 24, 2000
Date of Patent:
March 5, 2002
Assignee:
Warner-Lambert Company
Inventors:
Agnès Grouhel, Gilles Brunelle, François Roman, Jacques Hamon
Abstract: This invention provides a method for treating and preventing neurological disorder such as Alzheimer's disease, and for promoting wound healing comprising administering a compound characterized as being a matrix metalloproteinase inhibitor.
Type:
Grant
Filed:
March 19, 1999
Date of Patent:
January 22, 2002
Assignee:
Warner-Lambert Company
Inventors:
Thomas Michael Andrew Bocan, Peter Alan Boxer, Joseph Thomas Peterson, Jr., Denis Schrier, Andrew David White
Abstract: Described are neuroprotective agents of Formula I
wherein
R is an amino acid or nitrogen heterocyclic ring which is saturated or unsaturated of from 5 to 8 members which may have additional oxygen or sulfur atoms therein. The other provisions or substituents are described in the specification.
Type:
Grant
Filed:
November 25, 1998
Date of Patent:
January 22, 2002
Assignee:
Warner-Lambert Company
Inventors:
Brian Edward Kornberg, Sham Shridhar Nikam, Michael Francis Rafferty
Abstract: The invention is a series of 7-substituted quinazolin-2,4-diones useful as antibacterial agents, processes for the preparation of the compounds, and a pharmaceutical composition containing one or more of the compounds.
Type:
Grant
Filed:
March 15, 2000
Date of Patent:
December 18, 2001
Assignee:
Warner-Lambert Company
Inventors:
John Michael Domagala, Edmund Lee Ellsworth, Liren Huang, Thomas Eric Renau, Rajeshwar Singh, Michael Andrew Stier
Abstract: Compositions that comprise a GABA analog, such as gabapentin or pregabalin in combination with caffeine are disclosed. The compositions are used to treat pain in mammals.
Abstract: The present invention provides compounds that block calcium channels and have the Formula I:
and pharmaceutically acceptable salts, esters, and pro-drugs thereof, wherein
R1 and R2 are independently H, phenylcyclopentylcarbonyl, C1-C7 alkyl, cyclohexylmethyl, benzyl, C1-C5 alkylbenzyl, or C1-C5 alkoxybenzyl,
A is —C(O)— or —CH2—;
R3 is H or —CH3;
R4 is C1-C4 alkyl or piperidin-1-ylethyl;
R5 is phenyl-(CH2)n—, C1-C4 alkylphenyl-(CH2)n—, or halophenyl-(CH2)n—; and
n is 1 or 2.
The present invention also provides pharmaceutical compositions containing the compounds of Formula I and methods of using them to treat stroke, cerebral ischemia, head trauma, and epilepsy.
Abstract: Novel substituted amino acids of formula
are disclosed and are useful as agents in the treatment of epilepsy, faintness attacks, hypokinesia, cranial disorders, neurodegenerative disorders, depression, anxiety, panic, pain, and neuropathological disorders. Processes for the preparation and intermediates useful in the preparation are also disclosed.
Type:
Grant
Filed:
August 16, 2000
Date of Patent:
November 13, 2001
Assignee:
Warner-Lambert Company
Inventors:
Justin Stephen Bryans, David Christopher Horwell, Jean-Marie Receveur
Abstract:
The present invention provides novel N-type calcium channel blockers, compositions comprising them, and methods of their use. The compounds of the invention are useful in the treatment of stroke, cerebral ischemia, pain, epilepsy, and head trauma.
Abstract: Phenylamino benzoic acid, benzamides, and benzyl alcohol derivatives of the formula
where R1, R2, R3, R4, R5, and R6 are hydrogen or substituent groups such as alkyl, and where R7 is hydrogen or an organic radical, and Z is COOR7, tetrazolyl, CONR6R7, or CH2OR7, are potent inhibitors of MEK and, as such, are effective in treating cancer and other proliferative diseases such as inflammation, psoriasis and restenosis, as well as stroke, heart failure, and immunodeficiency disorders.
Type:
Grant
Filed:
January 5, 2000
Date of Patent:
October 30, 2001
Assignee:
Warner-Lambert Company
Inventors:
Stephen Douglas Barrett, Alexander James Bridges, Donna Reynolds Cody, Annette Marian Doherty, David Thomas Dudley, Alan Robert Saltiel, Mel Conrad Schroeder, Haile Tecle
Abstract: Inhibitors of protein farnesyl transferase enzymes are described, as well as methods for the preparation and pharmaceutical compositions of the same, which are useful in treating cancer, restenosis, psoriasis, endometriosis, atherosclerosis, or viral infections.
Type:
Grant
Filed:
November 2, 1998
Date of Patent:
October 9, 2001
Assignee:
Warner-Lambert Company
Inventors:
Ellen M. Dobrusin, Annette M. Doherty, James S. Kaltenbronn, Daniele M. Leonard, Dennis J. McNamara, Judith Sebolt-Leopold, Kevon R. Shuler
Abstract: Sulfonamide compounds are described which are inhibitors of matrix metalloproteinases, particularly stromelysin-1 and gelatinase A (72 kD gelatinase). Also described are methods for the treatment of multiple sclerosis, atherosclerotic plaque rupture, aortic aneurism, heart failure, restenosis, periodontal disease, corneal ulceration, burns, decubital ulcers, chronic ulcers or wounds, cancer metastasis, tumor angiogenesis, arthritis, or other autoimmune or inflammatory disorders dependent upon tissue invasion by leukocytes using the compounds.
Type:
Grant
Filed:
June 22, 2000
Date of Patent:
October 2, 2001
Assignee:
Warner-Lambert Company
Inventors:
Daniel F. Ortwine, Claude F. Purchase, Jr., Andrew D. White
Abstract: The present invention relates to compounds of Formula I that inhibit matrix metalloproteinases and to a method of inhibiting matrix metalloproteinases using the compounds.
wherein Q is an un-natural amino acid. More particurlarly, the present invention relates to a method of treating diseases in which matrix metalloproteinases are involved such as multiple sclerosis, atherosclerotic plaque rupture, restenosis, aortic aneurism, heart failure, periodontal disease, corneal ulceration, burns, decubital ulcers, chronic ulcers or wounds, cancer metastasis, tumor angiogenesis, arthiritis, or other autoimmune or inflammatory diseases dependent upon tissue invasion by leukocytes.
Type:
Grant
Filed:
March 2, 1999
Date of Patent:
September 25, 2001
Assignee:
Warner-Lambert Company
Inventors:
Joseph Armand Picard, Drago Robert Sliskovic
Abstract: Dyskinesias in humans are treated by administering a therapeutically effective dose of an NR1A/2B site-selective NMDA receptor antagonist compound to a human suffering therefrom.
Abstract: The present invention provides compounds having the Formula I
The present invention also provides methods of treating or preventing atherosclerosis, coronary heart disease, and restenosis using the compounds of Formula I, and pharmaceutical compositions comprising the compounds of Formula I.
Type:
Grant
Filed:
August 18, 1999
Date of Patent:
September 4, 2001
Assignee:
Warner-Lambert Company
Inventors:
Helen Tsenwhei Lee, Randy Ranjee Ramharack, Bruce David Roth, Karen Elaine Sexton