Abstract: The present invention relates to apoptosis signal-regulating kinase 1 (“ASK1”) inhibiting compounds of the formula wherein the variables are as defined herein. The invention also relates to pharmaceutical compositions, kits and articles of manufacture comprising such compounds; methods and intermediates useful for making the compounds; and methods of using said compounds.
Type:
Grant
Filed:
June 23, 2009
Date of Patent:
May 15, 2012
Assignee:
Takeda Pharmaceutical Company Limited
Inventors:
Edcon Chang, Stephen L. Gwaltney, Angie Vassar
Abstract: Compounds are provided for use with glucokinase that comprise the formula: wherein the variables are as defined herein. Also provided are pharmaceutical compositions, kits and articles of manufacture comprising such compounds; methods and intermediates useful for making the compounds; and methods of using said compounds.
Type:
Grant
Filed:
March 20, 2008
Date of Patent:
May 8, 2012
Assignee:
Takeda San Diego, Inc.
Inventors:
Zacharia Cheruvallath, Jun Feng, Prasuna Guntupalli, Stephen L. Gwaltney, Joanne Miura, Mark Sabat, Mingnam Tang
Abstract: Compounds of the following formula are provided for use with glucokinase: wherein the variables are as defined herein. Also provided are pharmaceutical compositions, kits and articles of manufacture comprising such compounds; methods and intermediates useful for making the compounds; and methods of using said compounds.
Type:
Grant
Filed:
December 17, 2007
Date of Patent:
April 24, 2012
Assignee:
Takeda San Diego, Inc.
Inventors:
Zacharia Cheruvallath, Jun Feng, Prasuna Guntupalli, Stephen L. Gwaltney, Joanne Miura, Mark Sabat, Mingnam Tang, Haxia Wang
Abstract: Disclosed are compounds, pharmaceutical compositions, kits, articles of manufacture, methods of using, and methods of preparing compounds having the formula: wherein the variables are as defined herein. The disclosed compounds are inhibitors of Renin.
Abstract: The invention relates to compounds having the formulae: wherein the variables are as defined herein. The invention further relates to methods of making and using these compounds, and pharmaceutical compositions, kits and articles of manufacture comprise the compounds.
Type:
Grant
Filed:
September 26, 2008
Date of Patent:
March 20, 2012
Assignee:
Takeda Pharmaceutical Company Limited
Inventors:
Benjamin Jones, Stephen W. Kaldor, Walter Keung, Andre A. Kiryanov, Zhe Li, Jeffrey A. Stafford, John Tyhonas, Craig Behnke
Abstract: The invention provides compounds, pharmaceutical compositions, kits, method of preparing, and method of using the compounds which exhibit renin and other S9 proteases activities and consist of the formula:—wherein the variables are as defined herein.
Type:
Grant
Filed:
March 11, 2008
Date of Patent:
March 13, 2012
Assignee:
Takeda Pharmaceutical Company Limited
Inventors:
Stephen L. Gwaltney, Zhiyuan Zhang, Betty Lam
Abstract: The invention relates to compounds having the formula: wherein the variables are as defined herein. The invention further relates to methods of making and using these compounds, and pharmaceutical compositions, kits and articles of manufacture comprise the compounds.
Abstract: Disclosed are compounds of the following formula: in which R1, R2, R5, R6, R7, R11, X, and m are defined in the specification. Also disclosed are pharmaceutical compositions, kits, and articles of manufacture, which contain the compounds, methods and intermediates useful for making the compounds, and methods of using the compounds to treat diseases, disorders, and conditions related to PARP activity.
Type:
Grant
Filed:
March 4, 2011
Date of Patent:
February 28, 2012
Assignee:
Takeda Pharmaceutical Company Limited
Inventors:
Anthony R. Gangloff, Andrew John Jennings, Benjamin Jones, Andre A. Kiryanov
Abstract: Disclosed are compounds of the following formula: in which R1, R2, R5, R6, R7, R31, u, and X are defined in the specification. Also disclosed are pharmaceutical compositions, kits, and articles of manufacture, which contain the compounds, methods and intermediates useful for making the compounds, and methods of using the compounds to treat diseases, disorders, and conditions related to PARP activity.
Type:
Grant
Filed:
January 21, 2010
Date of Patent:
April 19, 2011
Assignee:
Takeda Pharmaceutical Company Limited
Inventors:
Anthony R. Gangloff, Andrew John Jennings, Benjamin Jones, Andre A. Kiryanov
Abstract: Certain ?-amino acids that bind to the alpha-2-delta (?2?) subunit of a calcium channel are disclosed. These compounds and their pharmaceutically acceptable salts are useful in the treatment of a variety of psychiatric, pain and other disorders. Also disclosed are methods of making the ?-amino acids.
Type:
Grant
Filed:
December 7, 2006
Date of Patent:
June 17, 2008
Assignee:
Warner-Lambert Company LLC
Inventors:
Peter Garth Blazecka, Joseph Richard Bozelak, Norman Lloyd Colbry, Timothy Thomas Curran, Annise Paige Goodman, Kevin E. Henegar, Garrett Hoge, Paul D. Johnson, Augustine Tobi Osuma, Mark Stephen Plummer, Jacob Bradley Schwarz, Derek Clinton Vrieze, Ji Zhang
Abstract: P-chiral bisphospholane ligands and methods for their preparation are described. Use of metal/P-chiral bisphospholane complexes to catalyze asymmetric transformation reactions to provide high enantiomeric excesses of formed compounds is also described.
Type:
Grant
Filed:
May 10, 2004
Date of Patent:
June 12, 2007
Assignee:
Warner Lambert Company LLC
Inventors:
Garrett Stewart Hoge, II, Om Prakash Goel
Abstract: The invention is a novel series of cyclic amino acids which are useful in the treatment of epilepsy, faintness attacks, neurodegenerative disorders, depression, anxiety, panic, pain, neuropathological disorders, gastrointestinal disorders such as irritable bowel syndrome (IBS), and inflammation, especially arthritis. A pharmaceutical composition containing a compound of the invention as well as methods of preparing the compounds and novel intermediates useful in the preparation of the final compounds are included.
Type:
Grant
Filed:
March 11, 2005
Date of Patent:
October 17, 2006
Assignee:
Warner-Lambert Company
Inventors:
Justin Stephen Bryans, David Christopher Horwell, Andrew John Thorpe, David Juergen Wustrow, Po-Wai Yuen
Abstract: A process for synthesizing L and D-5,5,5,5?,5?,5?-hexafluoroleucine and protected analogs is disclosed. These compounds have utility in the preparation of fluorous peptides and proteins, which display interesting and unusual properties including strong self-association and an affinity for lipid bilayers.
Type:
Grant
Filed:
August 3, 2004
Date of Patent:
December 13, 2005
Assignee:
Warner-Lambert Company
Inventors:
James T. Anderson, Edward Neil Marsh, Peter Laurence Toogood
Abstract: The invention concerns a process for the preparation of N-aryl-aza-heterocycles of the general formula I by reaction of aza-heterocycles with activated aryl halides with use of caesium carbonate without addition of further catalysts at room temperature.
Type:
Grant
Filed:
July 15, 2004
Date of Patent:
August 23, 2005
Assignee:
Warner-Lambert Company
Inventors:
Hubert Barth, Klaus Steiner, Simon Schneider, Ulrich Bayer, Manfred Westermayer, Ulrike Wolfsperger, Hans-Jürgen Betche
Abstract: Methods and materials for preparing quinapril, its pharmaceutically acceptable salts, including quinapril hydrochloride, are disclosed. The method includes reacting (2S,4S)-2-(4-methyl-2,5-dioxo-oxazolidin-3-yl)-4-phenyl-butyric acid ethyl ester with (3S)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid tert-butyl ester to yield quinapril tert-butyl ester, which is subsequently reacted with an acid to yield quinapril or an acid addition salt of quinapril.
Abstract: Non-C2-symmetric bisphospholane ligands and methods for their preparation are described. Use of metal/non-C2-symmetric bisphospholane complexes to catalyze asymmetric transformation reactions to provide high enantiomeric excesses of formed compounds is also described.
Type:
Grant
Filed:
September 18, 2002
Date of Patent:
February 15, 2005
Assignee:
Warner-Lambert Company
Inventors:
Garrett Stewart Hoge, II, Om Prakash Goel
Abstract: A process for synthesizing L and D-5,5,5,5′,5′,5′-hexafluoroleucine and protected analogs is disclosed. These compounds have utility in the preparation of fluorous peptides and proteins, which display interesting and unusual properties including strong self-association and an affinity for lipid bilayers.
Type:
Grant
Filed:
September 16, 2003
Date of Patent:
September 7, 2004
Assignees:
Warner-Lambert Company LLC, The Regents of the University of Michigan
Inventors:
James T. Anderson, Edward Neil Marsh, Peter Laurence Toogood
Abstract: The invention concerns a process for the preparation of N-aryl-aza-heterocycles of the general formula I
by reaction of aza-heterocycles with activated aryl halides with use of caesium carbonate without addition of further catalysts at room temperature.
Type:
Grant
Filed:
February 7, 2002
Date of Patent:
August 10, 2004
Assignee:
Goedecke GmbH
Inventors:
Hubert Barth, Klaus Steiner, Simon Schneider, Ulrich Bayer, Manfred Westermayer, Ulrike Wolfsperger, Hans-Jürgen Betche
Abstract: P-chiral bisphospholane ligands and methods for their preparation are described. Use of metal/P-chiral bisphospholane complexes to catalyze asymmetric transformation reactions to provide high enantiomeric excesses of formed compounds is also described.
Type:
Grant
Filed:
April 18, 2003
Date of Patent:
June 15, 2004
Assignee:
Warner-Lambert Company LLC
Inventors:
Garrett Stewart Hoge, II, Om Prakash Goel
Abstract: Process for the preparation of symmetrical and asymmetrical carbonates of the general formula I
by reaction of alcohols of the general formula II and alkyl or aryl halides of the general formula III,
R—OH II
R′—HAL III
with carbon dioxide and caesium carbonate at room temperature in dipolar aprotic solvents.
Type:
Grant
Filed:
July 22, 2002
Date of Patent:
May 25, 2004
Assignee:
Goedecke GmbH
Inventors:
Hubert Barth, Klaus Steiner, Simon Schneider, Ulrich Bayer, Manfred Westermayer, Ulrike Wolfsperger