Authors:
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Trimble, LA
Silva, J
Chauret, N
Li, C
Therien, M
Grimm, E
Nicoll-Griffith, DA
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Therien, M
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Perrier, H
Prasit, P
Wang, ZI
Citation: M. Therien et al., Synthesis of rofecoxib, (MK 0966, Vioxx((R)) 4-(4 '-methylsulfonylphenyl)-3-phenyl-2(5H)-furanone), a selective and orally active inhibitor of cyclooxygenase-2, SYNTHESIS-S, (12), 2001, pp. 1778-1779
Authors:
Nicoll-Griffith, DA
Yergey, JA
Trimble, LA
Silva, JM
Li, C
Chauret, N
Gauthier, JY
Grimm, E
Leger, S
Roy, P
Therien, M
Wang, ZY
Prasit, P
Zamboni, R
Young, RN
Brideau, C
Chan, CC
Mancini, J
Riendeau, D
Citation: Da. Nicoll-griffith et al., Synthesis, characterization, and activity of metabolites derived from the cyclooxygenase-2 inhibitor rofecoxib (MK-0966, Vioxx (TM)), BIOORG MED, 10(23), 2000, pp. 2683-2686
Authors:
Li, CS
Black, WC
Brideau, C
Chan, CC
Charleson, S
Cromlish, WA
Claveau, D
Gauthier, JY
Gordon, R
Greig, G
Grimm, E
Guay, J
Lau, CK
Riendeau, D
Therien, M
Visco, DM
Wong, E
Xu, LJ
Prasit, P
Citation: Cs. Li et al., A new structural variation on the methanesulfonylphenyl class of selectivecyclooxygenase-2 inhibitors, BIOORG MED, 9(22), 1999, pp. 3181-3186
Authors:
Lau, CK
Brideau, C
Chan, CC
Charleson, S
Cromlish, WA
Ethier, D
Gauthier, JY
Gordon, R
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Kargman, S
Li, CS
Prasit, P
Riendeau, D
Therien, M
Visco, DM
Xu, LJ
Citation: Ck. Lau et al., Synthesis and biological evaluation of 3-heteroarizoxy-4-phenyl-2(5H)-furanones as selective COX-2 inhibitors, BIOORG MED, 9(22), 1999, pp. 3187-3192
Authors:
Frenette, R
Hutchinson, JH
Leger, S
Therien, M
Brideau, C
Chan, CC
Charleson, S
Ethier, D
Guay, J
Jones, TR
McAuliffe, M
Piechuta, H
Riendeau, D
Tagari, P
Girard, Y
Citation: R. Frenette et al., Substituted indoles as potent and orally active 5-lipoxygenase activating protein (FLAP) inhibitors, BIOORG MED, 9(16), 1999, pp. 2391-2396
Authors:
Prasit, P
Wang, Z
Brideau, C
Chan, CC
Charleson, S
Cromlish, W
Ethier, D
Evans, JF
Ford-Hutchinson, AW
Gauthier, JY
Gordon, R
Guay, J
Gresser, M
Kargman, S
Kennedy, B
Leblanc, Y
Leger, S
Mancini, J
O'Neill, GP
Ouellet, M
Percival, MD
Perrier, H
Riendeau, D
Rodger, I
Tagari, P
Therien, M
Vickers, P
Wong, E
Xu, LJ
Young, RN
Zamboni, R
Boyce, S
Rupniak, N
Forrest, N
Visco, D
Patrick, D
Citation: P. Prasit et al., The discovery of rofecoxib, [MK 966, Vioxx (R), 4-(4 '-methylsulfonylphenyl)-3-phenyl-2(5H)-furanone], an orally active cyclooxygenase-2 inhibitor, BIOORG MED, 9(13), 1999, pp. 1773-1778
Authors:
Chan, CC
Boyce, S
Brideau, C
Charleson, S
Cromlish, W
Ethier, D
Evans, J
Ford-Hutchinson, AW
Forrest, MJ
Gauthier, JY
Gordon, R
Gresser, M
Guay, J
Kargman, S
Kennedy, B
Leblanc, Y
Leger, S
Mancini, J
O'Neill, GP
Ouellet, M
Patrick, D
Percival, MD
Perrier, H
Prasit, P
Rodger, I
Tagari, P
Therien, M
Vickers, P
Visco, D
Wang, Z
Webb, J
Wong, E
Xu, LJ
Young, RN
Zamboni, R
Riendeau, D
Citation: Cc. Chan et al., Rofecoxib [Vioxx, MK-0966; 4-(4 '-methylsulfonylphenyl)-3-phenyl-2-(5H)-furanone]: A potent and orally active cyclooxygenase-2 inhibitor. Pharmacological and biochemical profiles, J PHARM EXP, 290(2), 1999, pp. 551-560