Abstract: Described herein is pyrrolo{2,3-d}pyrimidine compounds, their use as Janus Kinase (JAK) inhibitors, pharmaceutical compositions containing this compounds, and methods for the preparation of these compounds.
Type:
Grant
Filed:
August 17, 2009
Date of Patent:
March 13, 2012
Assignee:
Pfizer Inc.
Inventors:
Mark J. Mitton-Fry, Pamela J. Berlinski, Matthew J. Birchmeier, Jerry W. Bowman, Andrea Joy Gonzales, Steven Glenn Kamerling, Donald Wayne Mann
Abstract: This invention relates to a combination product comprising a range of 1-aryl-4 -cyclopropylpyrazoles in which there is at least one fluorine attached to the cyclopropyl ring, and one o more further therapeutic agents, particularly anti-parasitic agents.
Type:
Grant
Filed:
June 6, 2006
Date of Patent:
March 8, 2011
Assignee:
Pfizer Limited
Inventors:
Denis Billen, Nathan Anthony Logan Chubb, David Morris Gethin, Kim Thomas Hall, Lee Richard Roberts, Nigel Derek Arthur Walshe
Abstract: This invention relates to a range of alpha substituted 2-benzyl substituted imidazole compounds and pharmaceutically acceptable salts and solvates thereof, to compositions comprising such compounds, processes for their synthesis and their use as parasiticides.
Type:
Grant
Filed:
November 26, 2007
Date of Patent:
June 16, 2009
Assignee:
Pfizer Limited
Inventors:
Nathan Anthony Logan Chubb, Mark Roger Cox, Jerome Sebastien Dauvergne, Richard Andrew Ewin, Christelle Lauret
Abstract: This invention relates to a range of alpha substituted 2-benzyl substituted imidazole compounds and pharmaceutically acceptable salts and solvates thereof, to compositions comprising such compounds, processes for their synthesis and their use as parasiticides.
Type:
Grant
Filed:
November 26, 2007
Date of Patent:
June 9, 2009
Assignee:
Pfizer Limited
Inventors:
Nathan Anthony Logan Chubb, Mark Roger Cox, Jerome Sebastien Dauvergne, Richard Andrew Ewin, Christelle Lauret
Abstract: This invention relates to a combination product comprising a compound of formula I wherein X, R1, R2, R3, R4, R5, R6, R7 and R9 are as described herein, and one or more further biologically active compounds as described herein, particularly anti-parasitic agents.
Type:
Grant
Filed:
June 15, 2005
Date of Patent:
April 7, 2009
Assignee:
Pfizer Limited
Inventors:
Denis Billen, Nathan Anthony Logan Chubb, David Morris Gethin, Kim Thomas Hall, Lee Richard Roberts, Nigel Derek Arthur Walshe
Abstract: The present invention provides a compound of formula I or a pharmaceutically acceptable salt thereof wherein Y is —S(?O)n—, —S(?NR8)—, or —S(?NR8)(?O)—; Z is —NHC(?O)R1, —NHC(?S)R1, —NH-het1, —O-het1, —S-het1, or -het2. The compounds of formula I are useful as antibacterial agents.
Type:
Grant
Filed:
February 22, 2005
Date of Patent:
September 5, 2006
Assignee:
Pharmacia and Upjohn Company
Inventors:
Mikhail F. Gordeev, Adam Renslo, Gary W. Luehr, Stuart Lam, Neil E. Westlund, Dinesh Vinoobhai Patel
Abstract: The present invention is directed to novel amide-containing compounds which have an improved solubility and a method of improving the solubility of amide-containing compounds. The amide-containing compounds include oxazolidinone compounds and the bioavailability of these oxazolidinone compounds is improved by improving the solubility thereof.
Abstract: The present invention describes difluororthioacetamide oxazolidinones of formula I: R is —CH2— or —CH2CH2—; R2 and R3 are independently —H or —F; X is —CH—; Y is —SO—, —SO2—, or —SONR4—; and R4 is —H or —C1-4alkyl. These compounds are useful to treat infectives diseases caused by gram-positive and gram-negative bacteria.
Type:
Grant
Filed:
June 16, 2003
Date of Patent:
August 9, 2005
Assignee:
Pharmacia & Upjohn Company
Inventors:
Jackson Boling Hester, Jr., Wade J. Adams, Jeffrey Charles Stevens, Mikhail Fedor Gordeev, Upinder Singh, Carole Scott
Abstract: The present invention provides a compound of formula I which is useful as antiviral agents, in particular, as agents against viruses of the herpes family.
Type:
Grant
Filed:
December 18, 2002
Date of Patent:
June 7, 2005
Assignee:
Pharmacia & Upjohn Company
Inventors:
Fred L. Ciske, John R. Palmer, Mark E. Schnute, Valerie A. Vaillancourt
Abstract: The present invention provides a compound of formula I or a pharmaceutically acceptable salt thereof wherein A is a structure i, ii, iii, or iv X is CR7; Y is —S(?O)n—, —S(?NR8)—, or —S(?NR8)(?O)—; Z is —NHC(?O)R1, —NHC(?S)R1, —NR-het1, —O-het1, —S-het1, or -het2; and n is independently 0, 1, or 2. The compounds of formula I are useful as antimicrobials against a number of human and veterinary pathogens.
Type:
Grant
Filed:
January 21, 2003
Date of Patent:
April 26, 2005
Assignee:
Pharmacia & Upjohn Company
Inventors:
Mikhail F. Gordeev, Adam Renslo, Gary W. Luehr, Stuart Lam, Neil E. Westlund, Dinesh V. Patel
Abstract: The present invention provides certain thiadiazinone derivatives of oxazolidinones of the following formula I:
or pharmaceutically acceptable salts thereof that are antibacterial agents, pharmaceutical compositions containing them, methods for their use, and methods for preparing these compounds.
Type:
Grant
Filed:
February 4, 2003
Date of Patent:
December 7, 2004
Assignee:
Pharmacia & Upjohn Company
Inventors:
Gary W. Leuhr, Mikhail F. Gordeev, Dinesh V. Patel
Abstract: The present invention provides oxazinocarbazole derivatives having a ring connecting position 8 (C-8) and position 9 (N-9), and more specifically, provides compounds of formula (I) wherein R1, R2, R3 and R4 are described herein.
These compounds are 5-HT ligands, and are useful for treating diseases wherein modulation of 5-HT activity is desired.