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Results: 1-16 |
Results: 16
A SERIES OF NON-QUINOLINE CYSLT(1), RECEPTOR ANTAGONISTS - SAR STUDY ON PYRIDYL ANALOGS OF SINGULAIR(R)
Authors: GUAY D GAUTHIER JY DUFRESNE C JONES TR MCAULIFFE M MCFARLANE C METTERS KM PRASIT P ROCHETTE C ROY P SAWYER N ZAMBONI R
Citation: D. Guay et al., A SERIES OF NON-QUINOLINE CYSLT(1), RECEPTOR ANTAGONISTS - SAR STUDY ON PYRIDYL ANALOGS OF SINGULAIR(R), Bioorganic & medicinal chemistry letters, 8(5), 1998, pp. 453-458
SYNTHESIS AND BIOLOGICAL EVALUATION OF 5,6-DIARYLIMIDAZO[2.1-B]THIAZOLE AS SELECTIVE COX-2 INHIBITORS
Authors: THERIEN M BRIDEAU C CHAN CC CROMLISH WA GAUTHIER JY GORDON R GREIG G KARGMAN S LAU CK LEBLANC Y LI CS ONEILL GP RIENDEAU D ROY P WANG ZY XU LJ PRASIT P
Citation: M. Therien et al., SYNTHESIS AND BIOLOGICAL EVALUATION OF 5,6-DIARYLIMIDAZO[2.1-B]THIAZOLE AS SELECTIVE COX-2 INHIBITORS, Bioorganic & medicinal chemistry letters, 7(1), 1997, pp. 47-52
A NEW SERIES OF SELECTIVE COX-2 INHIBITORS - 5,6-DIARYLTHIAZOLO[3,2-B][1,2,4]TRIAZOLES
Authors: ROY P LEBLANC Y BALL RG BRIDEAU C CHAN CC CHAURET N CROMLISH W ETHIER D GAUTHIER JY GORDON R GREIG G GUAY J KARGMAN S LAU CK ONEILL G SILVA J THERIEN M VANSTADEN C WONG E XU L PRASIT P
Citation: P. Roy et al., A NEW SERIES OF SELECTIVE COX-2 INHIBITORS - 5,6-DIARYLTHIAZOLO[3,2-B][1,2,4]TRIAZOLES, Bioorganic & medicinal chemistry letters, 7(1), 1997, pp. 57-62
ONE-POT BIARYL SYNTHESIS VIA IN-SITU BORONATE FORMATION
Authors: GIROUX A HAN YX PRASIT P
Citation: A. Giroux et al., ONE-POT BIARYL SYNTHESIS VIA IN-SITU BORONATE FORMATION, Tetrahedron letters, 38(22), 1997, pp. 3841-3844
BIOCHEMICAL AND PHARMACOLOGICAL PROFILE OF A TETRASUBSTITUTED FURANONE AS A HIGHLY SELECTIVE COX-2 INHIBITOR
Authors: RIENDEAU D PERCIVAL MD BOYCE S BRIDEAU C CHARLESON S CROMLISH W ETHIER D EVANS J FALGUEYRET JP FORDHUTCHINSON AW GORDON R GREIG G GRESSER M GUAY J KARGMAN S LEGER S MANCINI JA ONEILL G OUELLET M RODGER IW THERIEN M WANG Z WEBB JK WONG E XU L YOUNG RN ZAMBONI R PRASIT P CHAN CC
Citation: D. Riendeau et al., BIOCHEMICAL AND PHARMACOLOGICAL PROFILE OF A TETRASUBSTITUTED FURANONE AS A HIGHLY SELECTIVE COX-2 INHIBITOR, British Journal of Pharmacology, 121(1), 1997, pp. 105-117
FROM INDOMETHACIN TO A SELECTIVE COX-2 INHIBITOR - DEVELOPMENT OF INDOLALKANOIC ACIDS AS POTENT AND SELECTIVE CYCLOOXYGENASE-2 INHIBITORS
Authors: BLACK WC BAYLY C BELLEY M CHAN CC CHARLESON S DENIS D GAUTHIER JY GORDON R GUAY D KARGMAN S LAU CK LEBLANC Y MANCINI J OUELLET M PERCIVAL D ROY P SKOREY K TAGARI P VICKERS P WONG E XU L PRASIT P
Citation: Wc. Black et al., FROM INDOMETHACIN TO A SELECTIVE COX-2 INHIBITOR - DEVELOPMENT OF INDOLALKANOIC ACIDS AS POTENT AND SELECTIVE CYCLOOXYGENASE-2 INHIBITORS, Bioorganic & medicinal chemistry letters, 6(6), 1996, pp. 725-730
NEW CLASS OF POTENT LIGANDS FOR THE HUMAN PERIPHERAL CANNABINOID RECEPTOR
Authors: GALLANT M DUFRESNE C GAREAU Y GUAY D LEBLANC Y PRASIT P ROCHETTE C SAWYER N SLIPETZ DM TREMBLAY N METTERS KM LABELLE M
Citation: M. Gallant et al., NEW CLASS OF POTENT LIGANDS FOR THE HUMAN PERIPHERAL CANNABINOID RECEPTOR, Bioorganic & medicinal chemistry letters, 6(19), 1996, pp. 2263-2268
SYNTHESIS AND BIOLOGICAL EVALUATION OF 2,3-DIARYLTHIOPHENES AS SELECTIVE COX-2 INHIBITORS .2. REPLACING THE HETEROCYCLE
Authors: GAUTHIER JY LEBLANC Y BLACK WC CHAN CC CROMLISH WA GORDON R KENNEDEY BP LAU CK LEGER S WANG ZY ETHIER D GUAY J MANCINI J RIENDEAU D TAGARI P VICKERS P WONG E XU LJ PRASIT P
Citation: Jy. Gauthier et al., SYNTHESIS AND BIOLOGICAL EVALUATION OF 2,3-DIARYLTHIOPHENES AS SELECTIVE COX-2 INHIBITORS .2. REPLACING THE HETEROCYCLE, Bioorganic & medicinal chemistry letters, 6(1), 1996, pp. 87-92
SYNTHESIS AND BIOLOGICAL EVALUATION OF 2,3-DIARYLTHIOPHENES AS SELECTIVE COX-2 AND COX-1 INHIBITORS
Authors: LEBLANC Y GAUTHIER JY ETHIER D GUAY J MANCINI J RIENDEAU D TAGARI P VICKERS P WONG E PRASIT P
Citation: Y. Leblanc et al., SYNTHESIS AND BIOLOGICAL EVALUATION OF 2,3-DIARYLTHIOPHENES AS SELECTIVE COX-2 AND COX-1 INHIBITORS, Bioorganic & medicinal chemistry letters, 5(18), 1995, pp. 2123-2128
PHARMACOLOGY OF A SELECTIVE CYCLOOXYGENASE-2 INHIBITOR, L-745,337 - ANOVEL NONSTEROIDAL ANTIINFLAMMATORY AGENT WITH AN ULCEROGENIC SPARINGEFFECT IN RAT AND NONHUMAN PRIMATE STOMACH
Authors: CHAN CC BOYCE S BRIDEAU C FORDHUTCHINSON AW GORDON R GUAY D HILL RG LI CS MANCINI J PENNETON M PRASIT P RASORI R RIENDEAU D ROY P TAGARI P VICKERS P WONG E RODGER IW
Citation: Cc. Chan et al., PHARMACOLOGY OF A SELECTIVE CYCLOOXYGENASE-2 INHIBITOR, L-745,337 - ANOVEL NONSTEROIDAL ANTIINFLAMMATORY AGENT WITH AN ULCEROGENIC SPARINGEFFECT IN RAT AND NONHUMAN PRIMATE STOMACH, The Journal of pharmacology and experimental therapeutics, 274(3), 1995, pp. 1531-1537
CYCLOOXYGENASE-2 INHIBITORS - SYNTHESIS AND PHARMACOLOGICAL ACTIVITIES OF 5-METHANESULFONAMIDO-1-INDANONE DERIVATIVES
Authors: LI CS BLACK WC CHAN CC FORDHUTCHINSON AW GAUTHIER JY GORDON R GUAY D KARGMAN S LAU CK MANCINI J OUIMET N ROY P VICKERS P WONG E YOUNG RN ZAMBONI R PRASIT P
Citation: Cs. Li et al., CYCLOOXYGENASE-2 INHIBITORS - SYNTHESIS AND PHARMACOLOGICAL ACTIVITIES OF 5-METHANESULFONAMIDO-1-INDANONE DERIVATIVES, Journal of medicinal chemistry, 38(25), 1995, pp. 4897-4905
STRUCTURAL REQUIREMENTS FOR THE BINDING OF FATTY-ACIDS TO 5-LIPOXYGENASE-ACTIVATING PROTEIN
Authors: CHARLESON S EVANS JF LEGER S PERRIER H PRASIT P WANG ZY VICKERS PJ
Citation: S. Charleson et al., STRUCTURAL REQUIREMENTS FOR THE BINDING OF FATTY-ACIDS TO 5-LIPOXYGENASE-ACTIVATING PROTEIN, European journal of pharmacology. Molecular pharmacology section, 267(3), 1994, pp. 275-280
SYNTHESIS OF A RADIOACTIVE PHOTOAFFINITY ARACHIDONIC-ACID ANALOG
Authors: PERRIER H PRASIT P WANG ZY
Citation: H. Perrier et al., SYNTHESIS OF A RADIOACTIVE PHOTOAFFINITY ARACHIDONIC-ACID ANALOG, Tetrahedron letters, 35(10), 1994, pp. 1501-1502
DISCOVERY OF INHIBITORS OF THE 5-LIPOXYGENASE ACTIVATING PROTEIN (FLAP)
Authors: YOUNG RN GILLARD JW HUTCHINSON JH LEGER S PRASIT P
Citation: Rn. Young et al., DISCOVERY OF INHIBITORS OF THE 5-LIPOXYGENASE ACTIVATING PROTEIN (FLAP), Journal of lipid mediators, 6(1-3), 1993, pp. 233-238
A NEW CLASS OF LEUKOTRIENE BIOSYNTHESIS INHIBITOR - THE DEVELOPMENT OF MK-0591
Authors: PRASIT P BELLEY M BLOUIN M BRIDEAU C CHAN C CHARLESON S EVANS JF FRENETTE R GAUTHIER JY GUAY J GILLARD JW GRIMM E FORDHUTCHINSON AW HUTCHINSON JH FORTIN R JONES TR MANCINI J LEGER S MCFARLANE CS PIECHUTA H RIENDEAU D ROY P TAGARI P VICKERS PJ YOUNG RN ZAMBONI R
Citation: P. Prasit et al., A NEW CLASS OF LEUKOTRIENE BIOSYNTHESIS INHIBITOR - THE DEVELOPMENT OF MK-0591, Journal of lipid mediators, 6(1-3), 1993, pp. 239-244
AN EFFICIENT SYNTHESIS OF LTD4 ANTAGONIST L-699,392
Authors: KING AO CORLEY EG ANDERSON RK LARSEN RD VERHOEVEN TR REIDER PJ XIANG YB BELLEY M LEBLANC Y LABELLE M PRASIT P ZAMBONI RJ
Citation: Ao. King et al., AN EFFICIENT SYNTHESIS OF LTD4 ANTAGONIST L-699,392, Journal of organic chemistry, 58(14), 1993, pp. 3731-3735
Risultati: 1-16 |