Abstract: Pyrimidine derivatives, which are useful as VEGFR2 inhibitors are described herein. The described invention also Includes methods of making such pyrimidine derivatives as well as methods of using the same in the treatment of hyperproliferative diseases.
Type:
Grant
Filed:
December 19, 2001
Date of Patent:
September 12, 2006
Assignee:
SmithKline Beecham Corporation
Inventors:
Amogh Boloor, Mui Cheung, Ronda Davis, Philip Anthony Harris, Kevin Hinkle, Robert Anthony Mook, Jr., Jeffery Alan Stafford, James Marvin Veal
Abstract: A compound of formula (I) or pharmaceutically acceptable salts and solvates thereof, for the treatment of a hPPAR mediated disease or condition
Type:
Grant
Filed:
May 9, 2002
Date of Patent:
August 15, 2006
Assignee:
SmithKline Beecham Corporation
Inventors:
Paul John Beswick, Christopher Charles Hamlett, Vipulkumar Patel, Michael Lawrence Sierra, Nigel Grahame Ramsden
Abstract: Compounds of formula (I) and pharmaceutically acceptable salts, solvates and hydrolysable esters thereof wherein X is O or S X1 is O or S; X is S or O; R1 and R2 are independently H, methyl, or halogen; R4 and R5 are independently H or C1-3 alkyl or R4 and R5 may, together with the carbon atom to which they are bonded, form a 3–5 membered cycloalkyl ring; R6 and R7 are independently H, C1-3 alkyl, or allyl; each R3 is independently halogen, C1-6 straight or branched alkyl, or CF3; and y is 0, 1, 2, 3, 4 or 5 act as hPPAR alpha agonists.
Abstract: A method of treating inflammatory diseases comprising administering 2-[2-methyl-4-[[[4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methyl]sulfanyl]phenoxy]acetic acid is disclosed.
Abstract: Compounds, compositions and methods for altering insulin secretion, particularly in the context of treatment of subjects having, or suspected of being at risk for having, diabetes mellitus. The compounds have the following structure (I): including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof, wherein W1, W2, X, R1, R2, R3, R4, m and n are defined herein.
Type:
Grant
Filed:
February 10, 2003
Date of Patent:
October 25, 2005
Assignee:
SmithKline Beecham Corporation
Inventors:
Yazhong Pei, Soumitra S. Ghosh, Ian William James
Abstract: The invention relates to pharmaceutical formulations and methods for preparing pharmaceutical formulations of histamine releasers. The present invention provides methods for determining the concentration of physiologically acceptable excipients for use in the formulations of the invention. The present invention also provides methods for suppressing pharmaceutically-induced histamine release by administering to an animal, the formulations of the present invention. A kit useful for preparing pharmaceutical formulations of histamine releasers is also provided.
Type:
Grant
Filed:
December 13, 2000
Date of Patent:
June 28, 2005
Assignee:
SmithKline Beecham Corporation
Inventors:
Alison G. Floyd, Mir A Hashim, Peiyuan Lin, Robert A. Mook, Andrea Sefler, Kathleen Cornell Meserve, Patricia Neal Ricciarelli, Timothy David Spitzer