AAAAAA

   
Results: 1-18 |
Results: 18
A NOVEL PHOTOAFFINITY PROBE FOR THE LTD4 RECEPTOR
Authors: GALLANT M SAWYER N METTERS KM ZAMBONI RJ
Citation: M. Gallant et al., A NOVEL PHOTOAFFINITY PROBE FOR THE LTD4 RECEPTOR, Bioorganic & medicinal chemistry, 6(1), 1998, pp. 63-72
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
CLONING AND CHARACTERIZATION OF THE 4 RAT EP PROSTANOID RECEPTOR SUBTYPES
Authors: BOIE Y STOCCO R SAWYER N SLIPETZ DM UNGRIN M NEUSCHAFERRUBE F PUSCHEL G METTERS KM ABRAMOVITZ M
Citation: Y. Boie et al., CLONING AND CHARACTERIZATION OF THE 4 RAT EP PROSTANOID RECEPTOR SUBTYPES, The FASEB journal, 11(9), 1997, pp. 2812-2812
MOLECULAR-CLONING AND CHARACTERIZATION OF THE 4 RAT PROSTAGLANDIN E-2PROSTANOID RECEPTOR SUBTYPES
Authors: BOIE Y STOCCO R SAWYER N SLIPETZ DM UNGRIN MD NEUSCHAFERRUBE F PUSCHEL GP METTERS KM ABRAMOVITZ M
Citation: Y. Boie et al., MOLECULAR-CLONING AND CHARACTERIZATION OF THE 4 RAT PROSTAGLANDIN E-2PROSTANOID RECEPTOR SUBTYPES, European journal of pharmacology, 340(2-3), 1997, pp. 227-241
STRUCTURE-ACTIVITY-RELATIONSHIPS OF TETRAHYDROCANNABINOL ANALOGS ON HUMAN CANNABINOID RECEPTORS
Authors: GAREAU Y DUFRESNE C GALLANT M ROCHETTE C SAWYER N SLIPETZ DM TREMBLAY N WEECH PK METTERS KM LABELLE M
Citation: Y. Gareau et al., STRUCTURE-ACTIVITY-RELATIONSHIPS OF TETRAHYDROCANNABINOL ANALOGS ON HUMAN CANNABINOID RECEPTORS, Bioorganic & medicinal chemistry letters, 6(2), 1996, pp. 189-194
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
DISCOVERY OF MK-0476, A POTENT AND ORALLY-ACTIVE LEUKOTRIENE D-4 RECEPTOR ANTAGONIST DEVOID OF PEROXISOMAL ENZYME-INDUCTION
Authors: LABELLE M BELLEY M GAREAU Y GAUTHIER JY GUAY D GORDON R GROSSMAN SG JONES TR LEBLANC Y MCAULIFFE M MCFARLANE C MASSON P METTERS KM OUIMET N PATRICK DH PIECHUTA H ROCHETTE C SAWYER N XIANG YB PICKETT CB FORDHUTCHINSON AW ZAMBONI RJ YOUNG RN
Citation: M. Labelle et al., DISCOVERY OF MK-0476, A POTENT AND ORALLY-ACTIVE LEUKOTRIENE D-4 RECEPTOR ANTAGONIST DEVOID OF PEROXISOMAL ENZYME-INDUCTION, Bioorganic & medicinal chemistry letters, 5(3), 1995, pp. 283-288
DISCOVERY OF L-740,515, A POTENT THIENOPYRIDINE CYSLT(1) RECEPTOR (LTD(4) RECEPTOR) ANTAGONIST
Authors: LABELLE M GAREAU Y DUFRESNE C LAU CK BELLEY M JONES TR LEBLANC Y MCAULIFFE M MCFARLANE CS METTERS KM OUIMET N PERRIER H ROCHETTE C SAWYER N SLIPETZ D XIANG YB WANG Z PICKETT CB FORDHUTCHINSON AW YOUNG RN ZAMBONI RJ
Citation: M. Labelle et al., DISCOVERY OF L-740,515, A POTENT THIENOPYRIDINE CYSLT(1) RECEPTOR (LTD(4) RECEPTOR) ANTAGONIST, Bioorganic & medicinal chemistry letters, 5(21), 1995, pp. 2551-2556
EVOLUTION OF A SERIES OF NON-QUINOLINE LEUKOTRIENE D-4 RECEPTOR ANTAGONIST - SYNTHESIS AND SAR OF BENZOTHIAZOLES AND THIAZOLES SUBSTITUTED BENZYL ALCOHOLS AS POTENT LTD(4) ANTAGONISTS
Authors: LAU CK DUFRESNE C GAREAU Y ZAMBONI R LABELLE M YOUNG RN METTERS KM ROCHETTE C SAWYER N SLIPETZ DM CHARETTE L JONES T MCAULIFFE M MCFARLANE C FORDHUTCHINSON AW
Citation: Ck. Lau et al., EVOLUTION OF A SERIES OF NON-QUINOLINE LEUKOTRIENE D-4 RECEPTOR ANTAGONIST - SYNTHESIS AND SAR OF BENZOTHIAZOLES AND THIAZOLES SUBSTITUTED BENZYL ALCOHOLS AS POTENT LTD(4) ANTAGONISTS, Bioorganic & medicinal chemistry letters, 5(15), 1995, pp. 1615-1620
MOLECULAR-CLONING AND CHARACTERIZATION OF THE HUMAN DP PROSTANOID RECEPTOR
Authors: BOIE Y SAWYER N SLIPETZ DM METTERS KM ABRAMOVITZ M
Citation: Y. Boie et al., MOLECULAR-CLONING AND CHARACTERIZATION OF THE HUMAN DP PROSTANOID RECEPTOR, The FASEB journal, 9(6), 1995, pp. 1373-1373
MOLECULAR-CLONING AND CHARACTERIZATION OF THE HUMAN PROSTANOID DP RECEPTOR
Authors: BOIE Y SAWYER N SLIPETZ DM METTERS KM ABRAMOVITZ M
Citation: Y. Boie et al., MOLECULAR-CLONING AND CHARACTERIZATION OF THE HUMAN PROSTANOID DP RECEPTOR, The Journal of biological chemistry, 270(32), 1995, pp. 18910-18916
PHARMACOLOGY OF MONTELUKAST SODIUM (SINGULAIR(TM)), A POTENT AND SELECTIVE LEUKOTRIENE D-4 RECEPTOR ANTAGONIST (VOL 73, PG 191, 1995)
Authors: JONES TR LABELLE M BELLEY M CHAMPION E CHARETTE L EVANS J FORDHUTCHINSON AW GAUTHIER JY LORD A MASSON P MCAULIFFE M MCFARLANE CS METTERS KM PICKETT C PIECHUTA H ROCHETTE C RODGER IW SAWYER N YOUNG RN ZAMBONI R ABRAHAM WM
Citation: Tr. Jones et al., PHARMACOLOGY OF MONTELUKAST SODIUM (SINGULAIR(TM)), A POTENT AND SELECTIVE LEUKOTRIENE D-4 RECEPTOR ANTAGONIST (VOL 73, PG 191, 1995), Canadian journal of physiology and pharmacology, 73(6), 1995, pp. 747-747
PHARMACOLOGY OF MONTELUKAST SODIUM (SINGULAIR(TM)), A POTENT AND SELECTIVE LEUKOTRIENE D-4 RECEPTOR ANTAGONIST
Authors: JONES TR LABELLE M BELLEY M CHAMPION E CHARETTE L EVANS J FORDHUTCHINSON AW GAUTHIER JY LORD A MASSON P MCAULIFFE M MCFARLANE CS METTERS KM PICKETT C PIECHUTA H ROCHETTE C RODGER IW SAWYER N YOUNG RN ZAMBONI R ABRAHAM WM
Citation: Tr. Jones et al., PHARMACOLOGY OF MONTELUKAST SODIUM (SINGULAIR(TM)), A POTENT AND SELECTIVE LEUKOTRIENE D-4 RECEPTOR ANTAGONIST, Canadian journal of physiology and pharmacology, 73(2), 1995, pp. 191-201
THE DISCOVERY OF L-699,392, A NOVEL POTENT AND ORALLY-ACTIVE LEUKOTRIENE D-4 RECEPTOR ANTAGONIST
Authors: LABELLE M BELLEY M CHAMPION E GORDON R HOOGSTEEN K JONES TR LEBLANC Y LORD A MCAULIFFE M MCFARLANE C MASSON P METTERS KM NICOLLGRIFFITH D OUIMET N PIECHUTA H ROCHETTE C SAWYER N XIANG YB YERGEY J FORDHUTCHINSON AW PICKETT CB ZAMBONI RJ YOUNG RN
Citation: M. Labelle et al., THE DISCOVERY OF L-699,392, A NOVEL POTENT AND ORALLY-ACTIVE LEUKOTRIENE D-4 RECEPTOR ANTAGONIST, Bioorganic & medicinal chemistry letters, 4(3), 1994, pp. 463-468
CHARACTERIZATION OF SPECIFIC BINDING-SITES FOR CYSTEINYL LEUKOTRIENESIN SHEEP LUNG
Authors: METTERS KM GAREAU Y LORD A ROCHETTE C SAWYER N
Citation: Km. Metters et al., CHARACTERIZATION OF SPECIFIC BINDING-SITES FOR CYSTEINYL LEUKOTRIENESIN SHEEP LUNG, The Journal of pharmacology and experimental therapeutics, 270(1), 1994, pp. 399-406
MICROSOMAL GLUTATHIONE-S-TRANSFERASE IS THE PREDOMINANT LEUKOTRIENE C-4 BINDING-SITE IN CELLULAR MEMBRANES
Authors: METTERS KM SAWYER N NICHOLSON DW
Citation: Km. Metters et al., MICROSOMAL GLUTATHIONE-S-TRANSFERASE IS THE PREDOMINANT LEUKOTRIENE C-4 BINDING-SITE IN CELLULAR MEMBRANES, The Journal of biological chemistry, 269(17), 1994, pp. 12816-12823
CLONING, FUNCTIONAL EXPRESSION, AND CHARACTERIZATION OF THE HUMAN PROSTAGLANDIN E(2) RECEPTOR EP(2) SUBTYPE
Authors: BASTIEN L SAWYER N GRYGORCZYK R METTERS KM ADAM M
Citation: L. Bastien et al., CLONING, FUNCTIONAL EXPRESSION, AND CHARACTERIZATION OF THE HUMAN PROSTAGLANDIN E(2) RECEPTOR EP(2) SUBTYPE, The Journal of biological chemistry, 269(16), 1994, pp. 11873-11877
DIALYSATE CALCIUM REDUCTION IN CAPD PATIENTS TREATED WITH CALCIUM-CARBONATE AND ALFACALCIDOL
Authors: CUNNINGHAM J BEER J COLDWELL RD NOONAN K SAWYER N MAKIN HLJ
Citation: J. Cunningham et al., DIALYSATE CALCIUM REDUCTION IN CAPD PATIENTS TREATED WITH CALCIUM-CARBONATE AND ALFACALCIDOL, Nephrology, dialysis, transplantation, 7(1), 1992, pp. 63-68
Risultati: 1-18 |