Andrew O. Stewart - Libertyville IL Steven A. Boyd - Mundelein IL David L. Arendsen - Libertyville IL Pramila Bhatia - Libertyville IL Kevin R. Condroski - Evanston IL Jennifer C. Freeman - Grayslake IL Indrani W. Gunawardana - Libertyville IL Kraig Lartey - Waukegan IL Catherine M. McCarty - Brookline MA Nicholas A. Mort - Highland Park IL Meena V. Patel - Chicago IL Michael A. Staeger - Greenfield WI David M. Stout - Libertyville IL
Assignee:
Abbott Laboratories - Abbott Park IL
International Classification:
A61K 31519
US Classification:
514258, 544278
Abstract:
Compounds having Formula I are useful for treating inflammation. Also disclosed are pharmaceutical compositions comprising compounds of Formula I, and methods of inhibiting/treating inflammatory diseases in a mammal.
Prostaglandin Endoperoxide H Synthase Biosynthesis Inhibitors
Lawrence A. Black - Libertyville IL, US Anwer Basha - Lake Forest IL, US Teodozyj Kolasa - Lake Villa IL, US Michael E. Kort - Lake Bluff IL, US Huaqing Liu - Buffalo Grove IL, US Catherine M. McCarty - Brookline MA, US Meena Patel - Chicago IL, US Jeffrey J. Rohde - Evanston IL, US Michael J. Coghlan - Grayslake IL, US Andrew O. Stewart - Libertyville IL, US
Assignee:
Abbott Laboratories - Abbott Park IL
International Classification:
A61K 31/50 A61K 31/675 C07D 237/16
US Classification:
514 85, 514247, 544232, 544240
Abstract:
The present invention describes pyridazinone compounds of formula I which are cyclooxygenase (COX) inhibitors, and in particular, are selective inhibitors of cyclooxygenase-2 (COX-2). COX-2 is the inducible isoform associated with inflammation, as opposed to the constitutive isoform, cyclooxygenase-1 (COX-1) which is an important “housekeeping” enzyme in many tissues, including the gastrointestinal (GI) tract and the kidneys. The selectivity of these compounds for COX-2 minimizes the unwanted GI and renal side-effects seen with currently marketed non-steroidal anti-inflammatory drugs (NSAIDs).
Prostaglandin Endoperoxide H Synthase Biosynthesis Inhibitors
Lawrence A. Black - Libertyville IL, US Anwer Basha - Lake Forest IL, US Teodozyj Kolasa - Lake Villa IL, US Michael E. Kort - Lake Bluff IL, US Huaqing Liu - Buffalo Grove IL, US Catherine M. McCarty - Brookline MA, US Meena Patel - Chicago IL, US Jeffrey J. Rohde - Evanston IL, US Michael J. Coghlan - Grayslake IL, US Andrew O. Stewart - Libertyville IL, US
Lawrence Black - Libertyville IL, US Anwer Basha - Lake Forest IL, US Teodozyj Kolasa - Lake Villa IL, US Michael Kort - Lake Bluff IL, US Huaqing Liu - Buffalo Grove IL, US Catherine McCarty - Brookline MA, US Meena Patel - Chicago IL, US Jeffrey Rohde - Evanston IL, US Michael Coghlan - Grayslake IL, US Andrew Stewart - Libertyville IL, US
International Classification:
A61K031/50 C07D237/14
US Classification:
514/248000, 544/240000
Abstract:
The present invention describes pyridazinone compounds of formula I which are cyclooxygenase (COX) inhibitors, and in particular, are selective inhibitors of cyclooxygenase-2 (COX-2). COX-2 is the inducible isoform associated with inflammation, as opposed to the constitutive isoform, cyclooxygenase-1 (COX-1) which is an important “housekeeping” enzyme in many tissues, including the gastrointestinal (GI) tract and the kidneys. The selectivity of these compounds for COX-2 minimizes the unwanted GI and renal side-effects seen with currently marketed non-steroidal anti-inflammatory drugs (NSAIDs).
Prostaglandin Endoperoxide H Synthase Biosynthesis Inhibitors
Lawrence Black - Libertville IL, US Anwer Basha - Lake Forest IL, US Teodozyj Kolasa - Lake Villa IL, US Michael Kort - Lake Bluff IL, US Huaqing Liu - Buffalo Grove IL, US Catherine McCarty - Brookline MA, US Meena Patel - Chicago IL, US Jeffrey Rohde - Evanston IL, US Michael Coghlan - Grayslake IL, US Andrew Stewart - Libertyville IL, US
International Classification:
C 07D 4 3/02 C07D237/14
US Classification:
544/238000, 544/239000
Abstract:
The present invention describes pyridazinone compounds of formula I which are cyclooxygenase (COX) inhibitors, and in particular, are selective inhibitors of cyclooxygenase-2 (COX-2). COX-2 is the inducible isoform associated with inflammation, as opposed to the constitutive isoform, cyclooxygenase-1 (COX-1) which is an important “housekeeping” enzyme in many tissues, including the gastrointestinal (GI) tract and the kidneys. The selectivity of these compounds for COX-2 minimizes the unwanted GI and renal side-effects seen with currently marketed non-steroidal anti-inflammatory drugs (NSAIDs).
Andrew Stewart - Libertyville IL, US Steven Boyd - Mundelein IL, US David Arendsen - Libertyville IL, US Pramila Bhatia - Libertyville IL, US Kevin Condroski - Evanston IL, US Jennifer Freeman - Grayslake IL, US Indrani Gunawardana - Libertyville IL, US Kraig Lartey - Waukegan IL, US Catherine McCarty - Brookline MA, US Nicholas Mort - Highland Park IL, US Meena Patel - Chicago IL, US Michael Staeger - Greenfield WI, US David Stout - Libertyville IL, US
Compounds having Formula I are useful for treating inflammation. Also disclosed are pharmaceutical compositions comprising compounds of Formula I, and methods of inhibiting/treating inflammatory diseases in a mammal.
Prostaglandin Endoperoxide H Synthase Biosynthesis Inhibitors
Lawrence A. Black - Libertyville IL, US Anwer Basha - Lake Forest IL, US Teodozyj Kolasa - Lake Villa IL, US Michael E. Kort - Lake Bluff IL, US Huaqing Liu - Buffalo Grove IL, US Catherine M. McCarty - Brookline MA, US Meena Patel - Chicago IL, US Jeffrey J. Rohde - Evanston IL, US Michael J. Coghlan - Grayslake IL, US Andrew O. Stewart - Libertyville IL, US
International Classification:
A61K 31/50 A61P 35/00
US Classification:
514247
Abstract:
The present invention describes pyridazinone compounds of formula Iwhich are cyclooxygenase (COX) inhibitors, and in particular, are selective inhibitors of cyclooxygenase-2 (COX-2). COX-2 is the inducible isoform associated with inflammation, as opposed to the constitutive isoform, cyclooxygenase-1 (COX-1) which is an important “housekeeping” enzyme in many tissues, including the gastrointestinal (GI) tract and the kidneys. The selectivity of these compounds for COX-2 minimizes the unwanted GI and renal side-effects seen with currently marketed non-steroidal anti-inflammatory drugs (NSAIDs).
Prostaglandin Endoperoxide H Synthase Biosynthesis Inhibitors
Lawrence A. Black - Libertyville IL Anwer Basha - Lake Forest IL Teodozyj Kolasa - Lake Villa IL Michael E. Kort - Lake Bluff IL Huaqing Liu - Buffalo Grove IL Catherine M. McCarty - Brookline MA Meena Patel - Chicago IL Jeffrey J. Rohde - Evanston IL Michael J. Coghlan - Grayslake IL Andrew O. Stewart - Libertyville IL
Assignee:
Abbott Laboratories - Abbott Park IL
International Classification:
C07D23716 C07F 96509 A61K 3150 A61K 31675
US Classification:
544240
Abstract:
The present invention describes pyridazinone compounds of formula I ##STR1## which are cyclooxygenase (COX) inhibitors, and in particular, are selective inhibitors of cyclooxygenase-2 (COX-2). COX-2 is the inducible isoform associated with inflammation, as opposed to the constitutive isoform, cyclooxygenase-1 (COX-1) which is an important "housekeeping" enzyme in many tissues, including the gastrointestinal (GI) tract and the kidneys. The selectivity of these compounds for COX-2 minimizes the unwanted GI and renal side-effects seen with currently marketed non-steroidal anti-inflammatory drugs (NSAIDs).