ACNP - Italian Periodicals Catalogue

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Results: 1-11 |

Results: 11

COMPARATIVE-STUDY OF HISTAMINE, LEUKOTRIENE D-4 (LTD4) AND ASCARIS-INDUCED CHANGES IN LUNG RESISTANCE (R-L) IN PROPOFOL (RAPINOVET(R))-ANESTHETIZED NON HUMAN PRIMATES

Authors: JONES TR PIECHUTA H MCAULIFFE M RASORI R PANNETON M BOSQUET J RODGER IW

Citation: Tr. Jones et al., COMPARATIVE-STUDY OF HISTAMINE, LEUKOTRIENE D-4 (LTD4) AND ASCARIS-INDUCED CHANGES IN LUNG RESISTANCE (R-L) IN PROPOFOL (RAPINOVET(R))-ANESTHETIZED NON HUMAN PRIMATES, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 3918-3918

EFFECTS OF A SELECTIVE PHOSPHODIESTERASE-IV INHIBITOR (CDP-840) IN A LEUKOTRIENE-DEPENDENT NONHUMAN PRIMATE MODEL OF ALLERGIC-ASTHMA

Authors: JONES TR MCAULIFFE M MCFARLANE CS PIECHUTA H MACDONALD D RODGER IW

Citation: Tr. Jones et al., EFFECTS OF A SELECTIVE PHOSPHODIESTERASE-IV INHIBITOR (CDP-840) IN A LEUKOTRIENE-DEPENDENT NONHUMAN PRIMATE MODEL OF ALLERGIC-ASTHMA, Canadian journal of physiology and pharmacology, 76(2), 1998, pp. 210-217

SUBSTITUTED (PYRIDYLMETHOXY)NAPHTHALENES AS POTENT AND ORALLY-ACTIVE 5-LIPOXYGENASE INHIBITORS - SYNTHESIS, BIOLOGICAL PROFILE, AND PHARMACOKINETICS OF L-739,010

Authors: HAMEL P RIENDEAU D BRIDEAU C CHAN CC DESMARAIS S DELORME D DUBE D DUCHARME Y ETHIER D GRIMM E FALGUEYRET JP GUAY J JONES TR KWONG E MCAULIFFE M MCFARLANE CS PIECHUTA H ROUMI M TAGARI P YOUNG RN GIRARD Y

Citation: P. Hamel et al., SUBSTITUTED (PYRIDYLMETHOXY)NAPHTHALENES AS POTENT AND ORALLY-ACTIVE 5-LIPOXYGENASE INHIBITORS - SYNTHESIS, BIOLOGICAL PROFILE, AND PHARMACOKINETICS OF L-739,010, Journal of medicinal chemistry, 40(18), 1997, pp. 2866-2875

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

THIOPYRANOL[2,3,4-C,D] INDOLES AS INHIBITORS OF 5-LIPOXYGENASE, 5-LIPOXYGENASE-ACTIVATING PROTEIN, AND LEUKOTRIENE C-4 SYNTHASE

Authors: HUTCHINSON JH CHARLESON S EVANS JF FALGUEYRET JP HOOGSTEEN K JONES TR KARGMAN S MACDONALD D MCFARLANE CS NICHOLSON DW PIECHUTA H RIENDEAU D SCHEIGETZ J THERIEN M GIRARD Y

Citation: Jh. Hutchinson et al., THIOPYRANOL[2,3,4-C,D] INDOLES AS INHIBITORS OF 5-LIPOXYGENASE, 5-LIPOXYGENASE-ACTIVATING PROTEIN, AND LEUKOTRIENE C-4 SYNTHASE, Journal of medicinal chemistry, 38(22), 1995, pp. 4538-4547

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

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

THIOPYRANO[2,3,4-CD]INDOLES AS 5-LIPOXYGENASE INHIBITORS - SYNTHESIS,BIOLOGICAL PROFILE, AND RESOLUTION OF RO-1H-THIOPYRANO[2,3,4-CD]INDOL-YL]ETHOXY]BUTANOIC ACID

Authors: HUTCHINSON JH RIENDEAU D BRIDEAU C CHAN C FALGUEYRET JP GUAY J JONES TR LEPINE C MACDONALD D MCFARLANE CS PIECHUTA H SCHEIGETZ J TAGARI P THERIEN M GIRARD Y

Citation: Jh. Hutchinson et al., THIOPYRANO[2,3,4-CD]INDOLES AS 5-LIPOXYGENASE INHIBITORS - SYNTHESIS,BIOLOGICAL PROFILE, AND RESOLUTION OF RO-1H-THIOPYRANO[2,3,4-CD]INDOL-YL]ETHOXY]BUTANOIC ACID, Journal of medicinal chemistry, 37(8), 1994, pp. 1153-1164

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

SUBSTITUTED THIOPYRANO[2,3,4-C,D]INDOLES AS POTENT, SELECTIVE, AND ORALLY-ACTIVE INHIBITORS OF 5-LIPOXYGENASE - SYNTHESIS AND BIOLOGICAL EVALUATION OF L-691,816

Authors: HUTCHINSON JH RIENDEAU D BRIDEAU C CHAN C DELORME D DENIS D FALGUEYRET JP FORTIN R GUAY J HAMEL P JONES TR MACDONALD D MCFARLANE CS PIECHUTA H SCHEIGETZ J TAGARI P THERIEN M GIRARD Y

Citation: Jh. Hutchinson et al., SUBSTITUTED THIOPYRANO[2,3,4-C,D]INDOLES AS POTENT, SELECTIVE, AND ORALLY-ACTIVE INHIBITORS OF 5-LIPOXYGENASE - SYNTHESIS AND BIOLOGICAL EVALUATION OF L-691,816, Journal of medicinal chemistry, 36(19), 1993, pp. 2771-2787

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