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Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
March 4, 1999
Oxidative bioactivation of the lactol prodrug of a lactone cyclooxygenase-2 inhibitor
D A Nicoll-Griffith, J P Falgueyret, J M Silva, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 18, 1999
Substituted heterocyclic analogs as selective COX-2 inhibitors in the flosulide class
N Ouimet, C C Chan, S Charleson, et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]
|
February 1, 1997
Characterization of autocrine inducible prostaglandin H synthase-2 (PGHS-2) in human osteosarcoma cells
E Wong, C DeLuca, C Boily, et al.
Clinical Pharmacology and Therapeutics
|
March 30, 1999
Characterization of rofecoxib as a cyclooxygenase-2 isoform inhibitor and demonstration of analgesia in the dental pain model
E W Ehrich, A Dallob, I De Lepeleire, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 1, 1999
Quinolines as potent 5-lipoxygenase inhibitors: synthesis and biological profile of L-746,530
D Dubé, M Blouin, C Brideau, et al.
Biochemical Pharmacology
|
October 11, 1996
Mechanism of selective inhibition of human prostaglandin G/H synthase-1 and -2 in intact cells
S Kargman, E Wong, G M Greig, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 7, 1999
Substituted indoles as potent and orally active 5-lipoxygenase activating protein (FLAP) inhibitors
R Frenette, J H Hutchinson, S Léger, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 28, 1999
SAR in the alkoxy lactone series: the discovery of DFP, a potent and orally active COX-2 inhibitor
Y Leblanc, P Roy, S Boyce, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 27, 1999
Synthesis and biological evaluation of 3-heteroaryloxy-4-phenyl-2(5H)-furanones as selective COX-2 inhibitors
C K Lau, C Brideau, C C Chan, et al.
Journal of Medicinal Chemistry
|
April 10, 1999
2,3-Diarylcyclopentenones as orally active, highly selective cyclooxygenase-2 inhibitors
W C Black, C Brideau, C C Chan, et al.
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of 8
Search research articles
Search
Showing results (61-70 of 78) with videos related to
Sort By:
Page
of 8
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
March 4, 1999
Oxidative bioactivation of the lactol prodrug of a lactone cyclooxygenase-2 inhibitor
D A Nicoll-Griffith, J P Falgueyret, J M Silva, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 18, 1999
Substituted heterocyclic analogs as selective COX-2 inhibitors in the flosulide class
N Ouimet, C C Chan, S Charleson, et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]
|
February 1, 1997
Characterization of autocrine inducible prostaglandin H synthase-2 (PGHS-2) in human osteosarcoma cells
E Wong, C DeLuca, C Boily, et al.
Clinical Pharmacology and Therapeutics
|
March 30, 1999
Characterization of rofecoxib as a cyclooxygenase-2 isoform inhibitor and demonstration of analgesia in the dental pain model
E W Ehrich, A Dallob, I De Lepeleire, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 1, 1999
Quinolines as potent 5-lipoxygenase inhibitors: synthesis and biological profile of L-746,530
D Dubé, M Blouin, C Brideau, et al.
Biochemical Pharmacology
|
October 11, 1996
Mechanism of selective inhibition of human prostaglandin G/H synthase-1 and -2 in intact cells
S Kargman, E Wong, G M Greig, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 7, 1999
Substituted indoles as potent and orally active 5-lipoxygenase activating protein (FLAP) inhibitors
R Frenette, J H Hutchinson, S Léger, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 28, 1999
SAR in the alkoxy lactone series: the discovery of DFP, a potent and orally active COX-2 inhibitor
Y Leblanc, P Roy, S Boyce, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 27, 1999
Synthesis and biological evaluation of 3-heteroaryloxy-4-phenyl-2(5H)-furanones as selective COX-2 inhibitors
C K Lau, C Brideau, C C Chan, et al.
Journal of Medicinal Chemistry
|
April 10, 1999
2,3-Diarylcyclopentenones as orally active, highly selective cyclooxygenase-2 inhibitors
W C Black, C Brideau, C C Chan, et al.
Page
of 8