Abstract: There are disclosed compounds of formula (I)
and pharmaceutically acceptable salts thereof which exhibit utility for the treatment of cytokine mediated diseases such as arthritis.
Type:
Grant
Filed:
June 12, 2000
Date of Patent:
June 11, 2002
Assignee:
Merck & Co., Inc.
Inventors:
Nigel J. Liverton, David A. Claremon, John W. Butcher, Cory R. Theberge
Abstract: Compounds of the formula I, in which R1, R2, R3?, R3, R4 and D have the meanings indicated in Claim 1, are inhibitors of tyrosine kinases, in particular Met kinase, and can be employed, inter alia, for the treatment of tumours.
Type:
Application
Filed:
April 24, 2009
Publication date:
March 24, 2011
Applicant:
Merck Patent Gesellschaft
Inventors:
Dieter Dorsch, Oliver Schadt, Frank Stieber, Andree Blaukat
Abstract: There are disclosed compounds of formula (I)
and pharmaceutically acceptable salts thereof which exhibit utility for the treatment of cytokine mediated diseases such as arthritis.
Type:
Grant
Filed:
November 4, 1999
Date of Patent:
February 26, 2002
Assignee:
Merck & Co., Inc.
Inventors:
David A. Claremon, Gerald S. Ponticello
Abstract: A purification method in the preparation of a substituted 8-arylquinoline, wherein the aryl group at the 8-position contains a substituent substituted-alkenyl group, utilizes a polystyrene-based sulfonylhydrazine reactive resin to remove an aldehyde impurity.
Type:
Grant
Filed:
September 12, 2003
Date of Patent:
July 21, 2009
Assignee:
Merck & Co. Inc.
Inventors:
Mirlinda Biba, Paul Compton Collins, Christopher Joseph Welch, David A. Conlon, Antoinette Drahus
Abstract: This invention relates to 3-Pyrimidinyl Bisnaphthalimides as Anticancer Agents and pharmaceutically acceptable salts thereof, of the formula: ##STR1## and processes for the preparation of such compounds, pharmaceutical composition containing such compounds, and methods of using such compounds to treat cancer, particularly solid tumor carcinomas, in mammals.
Abstract: The invention relates to a method of treating cocaine abuse or addiction in a mammal which comprises administering to the mammal an effective amount of a sigma receptor antagonist lacking or having relatively weak dopamine receptor-blocking activity, to reduce the pharmacological effects of the cocaine.
Abstract: The present invention is directed to compounds which inhibit farnesyl-protein transferase (FTase) and the farnesylation of the oncogene protein Ras. The invention is further directed to chemotherapeutic compositions containing the compounds of this invention and methods for inhibiting farnesyl-protein transferase and the farnesylation of the oncogene protein Ras.
Abstract: The present invention relates to substituted 1,3,8-triazaspiro[4.5]decame-2,4-diones useful as HIF prolyl hydroxylase inhibitors to treat anemia and like conditions.
Type:
Grant
Filed:
June 7, 2010
Date of Patent:
December 30, 2014
Assignee:
Merck Sharp & Dohme Corp.
Inventors:
Joan M. Pierce, Jeffrey J. Hale, Shouwu Miao, Petr Vachal
Abstract: The invention relates to novel compounds which comprise, as cationic or as anionic component, a pyrimidinecarboxylic acid derivative, in particular a derivative of ectoin or hydroxyectoin, to a process for the preparation thereof, and to the use thereof as ionic liquid or to the use thereof in pharmaceutical, cosmetic and dermatological formulations.
Type:
Application
Filed:
June 19, 2009
Publication date:
June 23, 2011
Applicant:
MERCK PATENT GESELLSCHAFT
Inventors:
Michael Howard Rayner-Branes, Thomas Rudolph, William-Robert Pitner, Jens Eichhorn
Abstract: The present invention relates to an improved method for controlling coccidiosis in poultry which comprises administering to poultry on shuttle medication an additional medication prior to switching from the starter compound to the grower compound, and continuing the additional medication for a period after the switching.
Abstract: Compounds of the formula I, in which R1, R2, R3, R3?, R4 and D have the meanings indicated in Claim 1, are inhibitors of tyrosine kinases, in particular Met kinase, and can be employed, inter alia, for the treatment of tumors.
Type:
Grant
Filed:
April 24, 2009
Date of Patent:
March 26, 2013
Assignee:
Merck Patent Gesellschaft Mit Beschrankter Haftung
Inventors:
Dieter Dorsch, Oliver Schadt, Frank Stieber, Andree Blaukat
Abstract: A class of substituted pyrimidine derivatives are ligands for dopamine receptor subtypes within the body and are therefore useful in the treatment of disorders of the dopamine system, in particular schizophrenia ##STR1##
Type:
Grant
Filed:
March 18, 1996
Date of Patent:
June 9, 1998
Assignee:
Merck, Sharp & Dohme Limited
Inventors:
William Robert Carling, Ian James Collins, Michael Rowley, Paul David Leeson
Abstract: Disclosed are the ERK inhibitors of formula 1.0: (Formula (A1)), and the pharmaceutically acceptable salts, esters and solvates thereof. Q is a piperidine ring that can have a bridge or a fused ring. All other substitutents are as defined herein. Also disclosed are methods of treating cancer using the compounds of formula A1.
Type:
Grant
Filed:
September 20, 2010
Date of Patent:
February 25, 2014
Assignee:
Merck Sharp & Dohme Corp.
Inventors:
Hugh Y. Zhu, Jagdish A. Desai, Alan B. Cooper, Ronald J. Doll
Abstract: Compounds of the formula I in which R1 and R2 have the meanings indicated in Claim 1, are inhibitors of Syk, and can be employed, inter alia, for the treatment of rheumatoid arthritis and/or systemic lupus
Type:
Application
Filed:
July 29, 2011
Publication date:
August 29, 2013
Applicant:
MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG
Inventors:
Lars Burgdorf, Melanie Schultz, Tatjana Ross, Brian Hodous, Justin Potnick, Amanda E. Sutton, Bayard R. Huck
Abstract: Female prenatal, neonatal and postnatal animals are treated with compositions containing steroid biosynthesis inhibitors or antagonists which prevents the conversion of androgens to estrogens. The compositions are useful for improving growth and feed efficiency.
Type:
Grant
Filed:
October 5, 1990
Date of Patent:
November 10, 1992
Assignee:
Merck & Co., Inc.
Inventors:
Alexander Elbrecht, Yi-Tien Yang, Roy G. Smith
Abstract: The present invention is related to a novel series of pyrimidyl or fused pyrimidyl hydrazones. Compounds of Formula (I) wherein A is selected from the group consisting of Formulas (A1), (A2), (A3), (A4), (A5) are useful for the treatment and/or prevention of a proliferative disease.
Type:
Application
Filed:
May 31, 2012
Publication date:
September 20, 2012
Applicant:
MERCK SERONO SA
Inventors:
BRIAN HEALEY, Zhong Zhao, Amanda Sutton, Matthias Schwarz
Abstract: N-aryl arylsulfonamide derivatives are bradykinin B1 antagonists or inverse agonists useful in the treatment or prevention of symptoms such as pain and inflammation associated with the bradykinin B1 pathway.
Type:
Grant
Filed:
June 30, 2004
Date of Patent:
July 1, 2008
Assignee:
Merck & Co., Inc.
Inventors:
Neville J. Anthony, John Jin Lim, Dai-shi Su, Michael R. Wood
Abstract: Compounds of the formula (I), in which X1, X2, X3, X4, R1, R2, R3 and R4 have the meanings indicated in Claim 1, are inhibitors of tyrosine kinases, in particular Met kinase, and can be employed, inter alia, for the treatment of tumours.
Type:
Application
Filed:
September 24, 2009
Publication date:
August 25, 2011
Applicant:
MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG
Abstract: The present invention relates to substituted 1,3,8-triazaspiro[4.5]decame-2,4-diones useful as HIF prolyl hydroxylase inhibitors to treat anemia and like conditions.
Type:
Application
Filed:
June 7, 2010
Publication date:
April 19, 2012
Applicant:
Merck Sharp & Dohme Corp.
Inventors:
Joan M. Pierce, Jeffrey J. Hale, Shouwu Miao, Petr Vachal