Abstract: Disclosed is a compound having the formula: pharmaceutically acceptable salts or solvates thereof and pharmaceutical compositions containing the same, wherein the structural variables are as defined herein. The compounds, salts and solvates of this invention are useful as LXR agonists.
Type:
Grant
Filed:
March 26, 2003
Date of Patent:
April 29, 2008
Assignee:
SmithKline Beecham Corporation
Inventors:
Ajita Bhat, John Jeffrey McAtee, Scott K. Thompson, James S. Frazee, Lara S. Kallander, Chun Ma, Joseph Marino, Michael J. Neeb, Robert A. Stavenger
Abstract: The present invention provides novel substituted isoxazole compounds, pharmaceutical compositions, therapeutic uses and processes for preparing the same.
Abstract: The present invention provides compounds that demonstrate protective effects on target cells from HIV infection in a manner as to bind to chemokine receptor, and which affect the binding of the natural ligand or chemokine to a receptor such as CXCR4 of a target cell.
Type:
Application
Filed:
July 29, 2005
Publication date:
April 24, 2008
Applicant:
SMITHKLINE BEECHAM CORPORATION
Inventors:
Kristjan Gudmundsson, John Franklin Miller, Elizabeth Madalena Turner
Abstract: The present invention relates to a novel human orphan nuclear receptor that binds to a cytochrome P-450 monoxygenase (CYP) promoter and that is activated by compounds that induce CYP gene expression. The invention further relates to nucleic acid sequences encoding such a receptor, to methods of making the receptor and to methods of using the receptor and nucleic acid sequences encoding same. The invention also relates to non-human animals transformed to express the human receptor and to methods of using such animals to screen compounds for drug interactions and toxicities.
Type:
Application
Filed:
June 22, 2007
Publication date:
April 24, 2008
Applicant:
SMITHKLINE BEECHAM CORPORATION
Inventors:
Steven Kliewer, Stacey Jones, Timothy Willson
Abstract: The present invention relates to novel compounds that are useful in the treatment of human papillomaviruses, and also to the methods for the making and use of such compounds.
Type:
Grant
Filed:
June 7, 2004
Date of Patent:
April 1, 2008
Assignee:
SmithKline Beecham Corporation
Inventors:
Sharon Davis Boggs, Kristjan S Gudmundsson, Leah D'Aurora Richardson, Paul Richard Sebahar
Abstract: Valve for an aerosol container for dispensing a suspension of a substance in a liquid propellant contained therein. The valve comprises a valve body (1) having at least one orifice (16) to allow a quantity of the suspension to pass from the container into the valve. The valve further comprises a ring (18) disposed around the valve body (1), the ring being positioned below the at least one orifice to reduce the volume of suspension that can be accommodated within the container below the at least one orifice when the container is orientated with the valve at the bottom, the ring having at least one portion of reduced axial thickness to provide a trough (19) around the valve body below the at least one orifice.
Type:
Grant
Filed:
April 15, 2005
Date of Patent:
April 1, 2008
Assignee:
SmithKline Beecham Corporation
Inventors:
Patrick Di Giovanni, Cheryl Vanessa Rogerson
Abstract: Untranslated regions associated with the heat shock response can be used to obtain increased efficiency of translation of polypeptides that are not necessarily normally associated with the heat shock response. This allows the development of greatly improved expression systems. The invention is also useful, for example, in the treatment of a patient suffering from a deficiency in the expression of a polypeptide and in the provision of vaccines.
Type:
Grant
Filed:
June 27, 2005
Date of Patent:
April 1, 2008
Assignee:
SmithKline Beecham Corporation
Inventors:
Herve Jean-Clement Coste, Jonathan Henry Ellis
Abstract: A medicament dispenser comprising: (i) a housing having an outlet; (ii) a medicament container locatable within said housing; (iii) an electronic dose counter associated with said outlet, wherein said dose counter comprises a first sensor for directly detecting a medicament release dispensible from said medicament container through said outlet is disclosed.
Type:
Grant
Filed:
October 19, 2001
Date of Patent:
March 25, 2008
Assignee:
Smithkline Beecham Corporation
Inventors:
Anthony Patrick Jones, Andrew Paul Horton, Richard William Hartley
Abstract: The invention relates to methods for the treatment of a sleep disorder comprising administering a compound of formula (I): wherein all variables are as defined herein.
Type:
Grant
Filed:
January 18, 2006
Date of Patent:
March 18, 2008
Assignee:
SmithKline Beecham Corporation
Inventors:
Giuseppe Alvaro, Romano Di Fabio, Riccardo Giovannini, Giuseppe Guercio, Yves St-Denis, Antonella Ursini
Abstract: The present invention is related to oxindole derivatives of structure (I), compositions containing the same, and methods of use and manufacture of the same. Such compounds generally are useful pharmacologically as agents in those disease states alleviated by the alteration of mitogen activated signaling pathways in general, and in particular in the inhibition or antagonism of protein kinases, which pathologically involve aberrant cellular proliferation. Such disease states include tumor growth, restenosis, atherosclerosis, pain and thrombosis. In particular, the present invention relates to a series of substituted oxindole compounds, which exhibit Trk family protein tyrosine kinase inhibition, and which are useful in cancer therapy and chronic pain indications.
Type:
Grant
Filed:
June 9, 2005
Date of Patent:
March 4, 2008
Assignee:
SmithKline Beecham Corporation
Inventors:
Karen Elizabeth Lackey, Edgar Raymond Wood, III
Abstract: A compound of formula (I) or a pharmaceutically acceptable salt, solvate, or hydrolysable ester thereof, wherein:
Type:
Grant
Filed:
June 18, 2003
Date of Patent:
March 4, 2008
Assignee:
SmithKline Beecham Corporation
Inventors:
Richard Bell, Paul John Beswick, Romain Luc Marie Gosmini, Richard Martin Grimes, Christopher Charles Frederick Hamlett, Nigel Paul King, Vipulkumar Kantibhai Patel
Abstract: Benzimidazole derivatives, which are useful as TIE-2 and/or VEGFR-2 inhibitors are described herein. The described invention also includes methods of making such benzimidazole derivatives as well as methods of using the same in the treatment of hyperproliferative diseases.
Type:
Grant
Filed:
February 28, 2003
Date of Patent:
March 4, 2008
Assignee:
SmithKline Beecham Corporation
Inventors:
Stanley Dawes Chamberlain, Mui Cheung, Holly Kathleen Emerson, Neil W. Johnson, Kristen Elizabeth Nailor, Douglas McCord Sammond, Marcus Semones
Abstract: The present invention is directed to novel compounds of formula (I): or pharmaceutically acceptable derivatives thereof, and their use as pharmaceuticals, particularly as p38 kinase inhibitors.
Type:
Application
Filed:
October 5, 2005
Publication date:
February 28, 2008
Applicant:
SMITHKLINE BEECHAM CORPORATION
Inventors:
Jeffrey Boehm, James Callahan, Zehong Wan, Hongxing Yan
Abstract: Invented are non-peptide TPO mimetics. Also invented are novel processes and intermediates used in the preparation of the presently invented compounds. Also invented is a method of treating thrombocytopenia, in a mammal, including a human, in need thereof which comprises administering to such mammal an effective amount of a selected hydroxy-1-azobenzene derivative.
Type:
Grant
Filed:
November 9, 2006
Date of Patent:
February 26, 2008
Assignee:
SmithKline Beecham Corporation
Inventors:
Kevin J. Duffy, Connie Erickson-Miller, Julian Jenkins, Juan I. Luengo, Sophie Visonneau
Abstract: A method of modulating KSP kinesin activity in vitro comprising contacting KSP kinesin with at least one chemical entity chosen from compounds represented by Formula I: and pharmaceutically acceptable salts thereof, where the variables are as defined further herein.
Abstract: Invented are non-peptide TPO mimetics. Also invented are novel processes and intermediates used in the preparation of the presently invented compounds. Also invented is a method of treating thrombocytopenia, in a mammal, including a human, in need thereof which comprises administering to such mammal an effective amount of a selected hydroxy-1-azobenzene derivative.
Type:
Grant
Filed:
January 5, 2007
Date of Patent:
February 19, 2008
Assignee:
SmithKline Beecham Corporation
Inventors:
Kevin J. Duffy, Connie Erickson-Miller, Julian Jenkins, Juan Luengo, Alan T. Price, Antony N. Shaw, Sophie Visonneau, Kenneth Wiggall
Abstract: A child resistant blister package includes a film having a surface wherein a plurality of cavities are formed therein containing at least one medicament; a cover sheet which overlies the cavities and is bonded to the film; and a wall structure raised above the surface of the film which extends throughout the film forming an interior region enclosing the plurality of cavities therein.
Abstract: This invention relates to the application of hydrophobic interaction chromatography combination chromatography to the purification of antibody molecule proteins.The questions raised in reexamination request, 09/006,966 filed Mar. 12, 2004 have been considered and the results thereof are reflected in this reissue patent which constitutes the reexamination certificate required by 35 U.S.C. 307 as provided in 37 CFR 1.570(e), for ex parte reexaminations, or the reexamination certificate required by 35 U.S.C. 316 as provided in 37 CFR 1.997(e) for inter partes reexaminations.
Type:
Grant
Filed:
May 27, 2005
Date of Patent:
February 19, 2008
Assignee:
SmithKline Beecham Corporation
Inventors:
Paula Shadle, John C. Erickson, Robert G. Scott, Thomas M. Smith