Abstract: The present invention provides a process for the preparation of 6-amino-4-(3-chloro-4-fluoro-phenylamino)-7-ethoxy-quinoline-3-carbonitrile comprising the steps and products disclosed within this application.
Type:
Grant
Filed:
September 10, 2004
Date of Patent:
April 29, 2008
Assignee:
Wyeth
Inventors:
Sylvain Daigneault, Ronald Stanley Michalak, Michel Bernatchez
Abstract: The present invention relates to uses of proteins that bind MK2 to modulate inflammation. More particularly, the invention relates to uses of proteins that bind MK2 for treating condition that are related to inflammation. The invention is useful for treating inflammatory conditions, particularly those in which a decrease in inflammation would be therapeutically beneficial.
Abstract: This invention relates to a method for the regioselective synthesis of 4,6,7,8-substituted benzo[g]quinoline-3-carbonitriles and 4,6,7,8-substituted benzo[g]quinazolines as well as intermediates thereof. The compounds derived from this invention are useful for the treatment of a variety of diseases that are a result of deregulation of these PTK's, and more specifically, are anti-cancer agents and are useful for the treatment of cancer in mammals. In addition, the compounds derived from this invention are useful for the treatment of polycystic kidney disease in mammals.
Type:
Grant
Filed:
December 11, 2001
Date of Patent:
April 29, 2008
Assignee:
Wyeth
Inventors:
Dan Maarten Berger, Gary Harold Birnberg, Yanong Wang
Abstract: This invention provides compounds of the formula: wherein A?, X and Y are defined in the specification. These compounds are useful as antibacterial agents.
Type:
Grant
Filed:
December 13, 2006
Date of Patent:
April 29, 2008
Assignee:
Wyeth
Inventors:
Phaik-Eng Sum, David Brian How, Darrin William Hopper, Matthew Douglas Vera, Joshua James Sabatini
Abstract: The instant invention provides compositions and methods for downmodulation of immune responses, e.g., autoimmune responses. For example, methods of downmodulating an immune response using agents that specifically block CD28-mediated signaling are provided. The subject methods are useful for both prophylactic and therapeutic downmodulation of immune responses.
Abstract: Sulfamoyl-containing compounds are disclosed, having utility as inhibitors of disease-related targets, such as Heat Shock Protein 90 (HSP90), and which are useful for treating disorders, e.g., proliferative disorders, including HSP90-mediated disorders. Methods for preparing and using the disclosed compounds are also described.
Type:
Application
Filed:
October 19, 2007
Publication date:
April 24, 2008
Applicant:
Wyeth
Inventors:
Jianxin Chen, Gerhard Sperl, Vincent Gullo, Lalitha Sista, Dallas Hughes, Yucai Peng, William Pierceall, Andrew Weiskopf, Jeremy Levin, Russell Dushin, Mercy Otteng
Abstract: Processes for preparing individual diastereomers of mono-pegylated rapamycin 42 ester with 3-hydroxy-2-(hydroxymethyl)-2-methylpropionic acid (CCI-779) are provided.
Abstract: A composition for delivery of osteogenic proteins is disclosed. The composition comprises an osteogenic protein, a calcium phosphate material as a carrier, and an effective amount of an effervescent agent. Methods of making the compositions and methods of using the osteogenic compositions to treat osteoporotic and/or osteopenic bone are also disclosed.
Type:
Application
Filed:
December 17, 2007
Publication date:
April 24, 2008
Applicants:
Wyeth, Etex Corporation
Inventors:
Rebecca Li, Howard Seeherman, Aliassghar Tofighi
Abstract: This invention relates to a method for recombinantly producing, via rescue of mumps virus, a nonsegmented, negative-sense, single-stranded RNA virus, and immunogenic compositions formed therefrom. Additional embodiments relate to methods of producing the mumps virus as an attenuated and/or infectious virus. The recombinant viruses are prepared from cDNA clones, and, accordingly, viruses having defined changes, including nucleotide/polynucleotide deletions, insertions, substitutions and re-arrangements, in the place of the genome are obtained.
Type:
Grant
Filed:
August 2, 2000
Date of Patent:
April 22, 2008
Assignee:
Wyeth
Inventors:
David K. Clarke, J. Erik Johnson, Mohinderjit S. Sidhu, Stephen A. Udem
Abstract: Mutant cholera holotoxins comprising a cholera toxin subunit A having single amino acid substitutions in the amino acid positions 16 or 72 or a double amino acid substitution in the amino acid positions 16 and 68 or 68 and 72 have reduced toxicity compared to the wild-type cholera holotoxin. The mutant cholera holotoxins are useful as adjuvants in immunogenic compositions to enhance the immune response in a vertebrate host to a selected antigen from a pathogenic bacterium, virus, fungus, or parasite, a cancer cell, a tumor cell, an allergen, or a self-molecule.
Type:
Grant
Filed:
December 15, 2006
Date of Patent:
April 22, 2008
Assignees:
Wyeth Holdings Corporation, The Regents of the University of Colorado, A Body Corporate
Inventors:
Bruce A. Green, Randall K. Holmes, Michael G. Jobling, Duzhang Zhu
Abstract: A stick lip balm with efficacious amounts of natural moisturizer and organoleptic/sensory attributes of lip feel associated with moisturizers and emollients is provided. The lip balm of the invention comprises at least 90% botanically derived materials and can be formed into a stick sufficiently robust to substantially retain the stick shape under normal conditions of shipping, storage and usage. A method of making the stick lip balm is also provided.
Type:
Application
Filed:
September 28, 2007
Publication date:
April 17, 2008
Applicant:
Wyeth
Inventors:
Sara Vest Magee, John Oliver Bachert, Neil Partridge, Jay R. Dickerson
Abstract: The invention relates to compounds, compositions comprising the compounds, and methods of using the compounds and compound compositions. The compounds, compositions, and methods described herein can be used for the therapeutic modulation of ion channel function, and treatment of disease and disease symptoms, particularly those mediated by certain calcium channel subtype targets.
Type:
Application
Filed:
December 12, 2007
Publication date:
April 17, 2008
Applicant:
Wyeth
Inventors:
Robert Zelle, Vincent Galullo, Hormoz Mazdiyasni
Abstract: Methods and compositions for inhibiting growth and differentiation factor-8 (GDF-8) activity in vitro and in vivo are provided. The methods and composition can be used for diagnosing, preventing, or treating degenerative disorders of muscle, bone, or glucose homeostasis.
Abstract: A genetic deletion mutant live E. coli vaccine suitable for mass application to poultry, including chickens, is provided. Also provided is a safe and effective method to protect poultry against the ravages of Escherichia coli bacillosis infection and disease in which a live mutant aroA-gene deleted E. coli immunogen is administered to chickens, turkeys and the like via mass application routes such as coarse sprays and drinking water.
Type:
Grant
Filed:
May 3, 2004
Date of Patent:
April 15, 2008
Assignee:
Wyeth
Inventors:
Henry H. Fan, Mahesh Kumar, Roberto Marcello La Ragione, Martin John Woodward
Abstract: Thioamide compounds, and specifically, thioamide pyrrole compounds, and preparation thereof are provided. These thioamide compounds can be used as progesterone receptor modulators, in contraception, and in the treatment of progesterone-related maladies.
Abstract: The present invention provides a compound of formula I and the use thereof in the therapeutic treatment of a CNS disorder related to or affected by the 5-HT6 receptor.
Abstract: This invention provides compounds of Formula (I), having the structure where G1, G2, G3, G4, A1, A2, Y1, Y2, L1, Z, e and f are defined herein, or a pharmaceutically acceptable salt thereof, which are useful for treating or preventing cancer.
Abstract: The present invention is directed to arylamino-arylpropanolamine derivatives of formula I: or a pharmaceutically acceptable salt thereof, compositions containing these derivatives, and methods of their use for the prevention and treatment of conditions ameliorated by monoamine reuptake including, inter alia, vasomotor symptoms (VMS), sexual dysfunction, gastrointestinal and genitourinary disorders, chronic fatigue syndrome, fibromyalgia syndrome, nervous system disorders, and combinations thereof, particularly those conditions selected from the group consisting of major depressive disorder, vasomotor symptoms, stress and urge urinary incontinence, fibromyalgia, pain, diabetic neuropathy, and combinations thereof.
Type:
Application
Filed:
October 2, 2007
Publication date:
April 10, 2008
Applicant:
Wyeth
Inventors:
An Thien Vu, Stephen Todd Cohn, Eugene Anthony Terefenko, William Jay Moore, Puwen Zhang, Paige Erin Mahaney, Eugene John Trybulski
Abstract: The present invention relates to identification of agents that pay a role in regulating brain amyloid-? (A?) levels in vivo. The invention provides compounds and methods of using such compounds to treat amyloidogenic conditions. It also provides a useful animal model for screening for and evaluating candidate amyloid inhibiting or therapeutic compounds. In particular, ovariectomy (ovx) and estrogen replacement were found to affect brain A?, levels in guinea pigs. Long-term ovx of guinea pigs resulted in increased levels of total brain A?, as compared to intact animals, and the A?42/A?40 ratio was also elevated. Treatment of ovx guinea pigs with ?17-estradiol for ten days partially reversed the ovx-associated increase in brain A? levels.
Type:
Application
Filed:
December 7, 2007
Publication date:
April 10, 2008
Applicants:
Wyeth, Nathan S. Kline Research Institute
Inventors:
Suzana Petanceska, Sam Gandy, Donald Frail