Abstract: Disclosed are compounds represented by formulae I, II, and III, and the compositions and methods thereof for treating viral infections caused by a Flaviviridae family virus.
Abstract: Artificial chromosomes, including ACes, that have been engineered to contain available sites for site-specific, recombination-directed integration of DNA of interest are provided. These artificial chromosomes permit tractable, efficient, rational engineering of the chromosome for a variety of applications.
Type:
Grant
Filed:
December 6, 2004
Date of Patent:
April 21, 2009
Assignee:
SmithKline Beecham Corporation
Inventors:
Edward Perkins, Carl Perez, Michael Lindenbaum, Amy Greene, Josephine Leung, Elena Fleming, Sandra Stewart
Abstract: The present invention relates to novel pharmaceutical aerosol formulations comprising: (A) a therapeutic agent in the form of particles coated by at least one coating excipient and at least one surfactant, in suspension in (B) a liquefied propellant gas for the administration of therapeutic agents particularly by the pulmonary route and to process for preparing these formulations. It also relates to novel particles suitable for use in such formulations.
Type:
Grant
Filed:
February 11, 2003
Date of Patent:
April 21, 2009
Assignee:
SmithKline Beecham Corporation
Inventors:
Pascal Cavaillon, Nathalie Llorca, Olivier Louis, Patrick Rosier
Abstract: The invention provides an isolated protein which is a member of the TNF ligand superfamily and comprising: i) a polypeptide having the amino acid sequence of figure (1); or ii) a variant of the polypeptide of i).
Type:
Application
Filed:
November 26, 2008
Publication date:
April 16, 2009
Applicant:
SMITHKLINE BEECHAM CORPORATION
Inventors:
Stuart Neville Farrow, Allard Kaptein, Jeremy David Alisdair Kitson, Alison Janet Winder
Abstract: This invention relates to novel compounds and compositions thereof, useful in the treatment of disease states mediated by the chemokine, Interleukin-8 (IL-8).
Abstract: Compounds of formula (I): are inhibitors of p38 kinase and are useful in the treatment of conditions or disease states mediated by p38 kinase activity or mediated by cytokines produced by the activity of p38.
Type:
Grant
Filed:
August 7, 2006
Date of Patent:
April 7, 2009
Assignee:
SmithKline Beecham Corporation
Inventors:
Nicola Mary Aston, Paul Bamborough, Ann Louise Walker
Abstract: The present invention provides compounds of formula (I): wherein all variables are as defined herein, pharmaceutical compositions containing the same, processes for preparing the same and their use as pharmaceutical agents.
Type:
Grant
Filed:
February 11, 2004
Date of Patent:
April 7, 2009
Assignee:
SmithKline Beecham Corporation
Inventors:
Ronda Davis-Ward, Robert Anthony Mook, Jr., Michael J Neeb, James M Salovich
Abstract: The invention relates to new methods of preparing substituted benzimidazole compounds, such as 2-bromo-5,6-dichlorobenzimidazole, which are useful in the preparation of compounds having antiviral activity.
Abstract: This invention relates to non-steroidal compounds that are modulators of androgen, glucocorticoid, mineralocorticoid, and progesterone receptors, and also to the methods for the making and use of such compounds.
Type:
Grant
Filed:
March 3, 2005
Date of Patent:
April 7, 2009
Assignee:
SmithKline Beecham Corporation
Inventors:
Philip Stewart Turnbull, Rodolfo Cadilla, David John Cowan, Andrew Lamont Larkin, Istvan Kaldor, Eugene Lee Stewart
Abstract: Heteroaromatic compounds are described, methods for their preparation, pharmaceutical compositions containing them, methods of use, and their use in medicines. In particular, the invention relates to quinazoline and pyridopyrimidine derivatives which exhibit protein tyrosine kinase inhibition.
Type:
Grant
Filed:
August 1, 2007
Date of Patent:
March 24, 2009
Assignee:
SmithKline Beecham Corporation
Inventors:
George Stuart Cockerill, Karen Elizabeth Lackey
Abstract: This invention relates to novel humanized and other recombinant or engineered antibodies or monoclonal antibodies to the vitronectin ?v?3 receptor and to the genes encoding same. Such antibodies are useful for the therapeutic and/or prophylactic treatment of ?v?3-mediated disorders, such as restenosis, in human patients.
Type:
Grant
Filed:
October 18, 2006
Date of Patent:
March 17, 2009
Assignee:
SmithKline Beecham Corporation
Inventors:
Zdenka L Jonak, Kyung O Johanson, Alexander Taylor
Abstract: Provided herein are certain substituted N-phenethylbenzamide of formula V: that may be useful for treating certain cellular proliferation diseases and disorders by modulating the activity of CENP-E.
Abstract: Amino acids (136 to 142) and amino acids (162 to 168) of human osteopontin constitute two sites at which osteopontin interacts with ?4 integrins. Products capable of disrupting those interactions are useful in therapy, particularly in the treatment of inflammatory diseases.
Type:
Grant
Filed:
March 23, 2001
Date of Patent:
March 17, 2009
Assignee:
Smithkline Beecham Corporation
Inventors:
Simon Barry, Carmel Horgan, Steven Ludbrook
Abstract: The present invention relates generally to novel therapeutic compounds and AXOR 109 agonists, and processes for the manufacture and use of the same.
Type:
Application
Filed:
January 19, 2007
Publication date:
March 12, 2009
Applicant:
SMITHKLINE BEECHAM CORPORATION
Inventors:
Jerzy Ryszard Szewczyk, Christopher P. Laudeman, Thomas Dock, Zibin Chen, Anderson Evans, Yue H. Li
Abstract: The present invention relates to aminopyrazine derivatives, compositions and medicaments containing the same, as well as processes for the preparation and use of such compounds, compositions and medicaments. Such aminopyrazine derivatives are useful in the treatment of diseases associated with inappropriate tyrosine and/or serine/threonine kinase activity.
Type:
Application
Filed:
October 31, 2008
Publication date:
March 5, 2009
Applicant:
SMITHKLINE BEECHAM CORPORATION
Inventors:
Michael John Alberti, David Harold Drewry, David Drysdale Miller, Paul Bamborough
Abstract: The present invention relates to a compound represented by Formula (I): and pharmaceutically acceptable salts. Compounds of the present invention inhibit Aurora kinase, making them especially suitable for the treatment of a number of diseases, including solid tumor cancers and hematological cancers.
Type:
Grant
Filed:
September 14, 2007
Date of Patent:
February 24, 2009
Assignee:
SmithKline Beecham Corporation
Inventors:
Martha A. Sarpong, Nicholas D. Adams, Jeffrey Michael Axten, Amita M. Chaudhari, Dashyant Dhanak, Toshihiro Hamajima, Kenneth Allen Newlander, Cynthia A. Parrish, Jerry Leroy Adams, Domingos J. Silva, Jun Tang
Abstract: A crystal structure of the cfms kinase domain, co-crystal structure with a bound small molecule, as well as methods of using the same in the discovery of cfms inhibitors and in the treatment of diseases mediated by inappropriate cfms activity.
Type:
Grant
Filed:
May 9, 2006
Date of Patent:
February 17, 2009
Assignee:
SmithKline Beecham Corporation
Inventors:
Holly Kathleen Emerson, David Lee Musso, Stanley Dawes Chamberlain, Gregory Edward Peckham
Inventors:
Andrew McDonald, Gustave Bergnes, Bainian Feng, David J. Morgans, Jr., Steven David Knight, Kenneth A. Newlander, Dashyant Dhanak, Christopher A. Brook