Abstract: Disclosed are compounds having Formula (I) and the compositions and methods thereof for treating or preventing a viral infection mediated at least in part by a virus in the Flaviviridae family of viruses, wherein A, R2, m, R, V, W, T, Z, R1, Y, and p are disclosed herein.
Type:
Grant
Filed:
December 12, 2006
Date of Patent:
September 29, 2009
Assignee:
SmithKline Beecham Corporation
Inventors:
Franz Ulrich Schmitz, Christopher Don Roberts, Ali Dehghani Mohammad Abadi, Ronald Conrad Griffith, Martin Robert Leivers, Irina Slobodov, Roopa Rai
Abstract: A compound of formula (I) wherein: R is a group selected from: A-B is a bivalent radical of formula (v), (vi) or (vii) —CH?C(R11)—??(v) —C(R10)?CH— or??(vi) —C(R12)(R10)—C(R11)(R13)—??(viii) and all other variables are as defined herein or a pharmaceutically acceptable salt or solvate thereof, process for their preparation and their use in the treatment of conditions mediated by tachykinins and/or by selective inhibition of serotonin reuptake transporter protein.
Abstract: The present invention relates to piperidine derivatives of formula (I): wherein R, R1, R2, R3, R4, R5, R6, X, Y, m and n are as defined herein; and pharmaceutically acceptable salts and solvates thereof; the process for their preparation and their use in the treatment of conditions mediated by tachykinins.
Type:
Grant
Filed:
February 5, 2003
Date of Patent:
January 27, 2009
Assignee:
Glaxo Group Limited
Inventors:
Giuseppe Alvaro, Alfredo Paio, Alessandro Pontiroli, Simone Spada, Maria Elvira Tranquillini
Abstract: The present invention includes anhydrous crystalline forms of (2S,4S)-4-fluoro-1-[4-fluoro-?-(4-fluorophenyl)-L-phenylalanyl]-2-pyrrolidinecarbonitrile p-toluenesulfonic acid salt.
Type:
Grant
Filed:
July 19, 2004
Date of Patent:
December 9, 2008
Assignee:
SmithKline Beecham Corporation
Inventors:
David H Igo, Paul R Johnson, Daniel E Patterson, Amarjit Sab Randhawa
Abstract: Compounds of formula (I) or derivatives thereof: wherein A, B, Z, R1, R2a, R2b, Rx, R8, and R9 are as defined in the specification, a process for the preparation of such compounds, pharmaceutical compositions comprising such compounds and the use of such compounds in medicine.
Type:
Grant
Filed:
October 30, 2003
Date of Patent:
November 4, 2008
Assignee:
Glaxo Group Limited
Inventors:
Rino Antonio Bit, Gerard Martin Paul Giblin, Adrian Hall, David Nigel Hurst, Ian Reginald Kilford, Neil Derek Miller, Tiziana Scoccitti
Abstract: The invention relates to compounds of formula (I) processes for their preparation, pharmaceutical compositions containing them and to their use in medicine, particularly use in the amelioration of a clinical condition for which a Factor Xa inhibitor is indicated.
Type:
Grant
Filed:
October 11, 2006
Date of Patent:
September 30, 2008
Assignee:
Glaxo Group Limited
Inventors:
Chuen Chan, Julie Nicole Hamblin, Henry Anderson Kelly, Nigel Paul King, Andrew McMurtrie Mason, Vipulkumar Kantibhai Patel, Stefan Senger, Gita Punjabhai Shah, Nigel Stephen Watson, Helen Elisabeth Weston, Caroline Whitworth, Robert John Young
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: The present invention involves a novel crystal form of 17?-hydroxy-7?-(5?-methyl-2?-furyl)-pregna-4,9(11)-dien-3-one-21-carboxylic acid, ?-lactone, having the formula which is an intermediate useful in preparation of an important pharmaceutical, eplerenone.
Type:
Grant
Filed:
September 19, 2003
Date of Patent:
September 26, 2006
Assignee:
Pharmacia Corporation
Inventors:
Bruce Allen Pearlman, Frederick J. Antosz