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Results: 1-16 |
Results: 16
EXPERIMENTAL-DESIGN FOR HIGH-THROUGHPUT SCREENING
Authors: LUTZ MW MENIUS JA CHOI TD LASKODY RG DOMANICO PL GOETZ AS SAUSSY DL
Citation: Mw. Lutz et al., EXPERIMENTAL-DESIGN FOR HIGH-THROUGHPUT SCREENING, Drug discovery today, 1(7), 1996, pp. 277-286
STRUCTURE-ACTIVITY-RELATIONSHIPS OF A SERIES OF BUSPIRONE ANALOGS AT ALPHA-1-ADRENOCEPTORS - FURTHER EVIDENCE THAT RAT AORTA ALPHA-1-ADRENOCEPTORS ARE OF THE ALPHA-1D-SUBTYPE
Authors: SAUSSY DL GOETZ AS QUEEN KL KING HK LUTZ MW RIMELE TJ
Citation: Dl. Saussy et al., STRUCTURE-ACTIVITY-RELATIONSHIPS OF A SERIES OF BUSPIRONE ANALOGS AT ALPHA-1-ADRENOCEPTORS - FURTHER EVIDENCE THAT RAT AORTA ALPHA-1-ADRENOCEPTORS ARE OF THE ALPHA-1D-SUBTYPE, The Journal of pharmacology and experimental therapeutics, 278(1), 1996, pp. 136-144
PHENYLALANINE IN THE 2ND-MEMBRANE-SPANNING DOMAIN OF ALPHA(1A)-ADRENERGIC RECEPTOR DETERMINES SUBTYPE SELECTIVITY OF DIHYDROPYRIDINE ANTAGONISTS
Authors: HAMAGUCHI N TRUE TA SAUSSY DL JEFFS PW
Citation: N. Hamaguchi et al., PHENYLALANINE IN THE 2ND-MEMBRANE-SPANNING DOMAIN OF ALPHA(1A)-ADRENERGIC RECEPTOR DETERMINES SUBTYPE SELECTIVITY OF DIHYDROPYRIDINE ANTAGONISTS, Biochemistry, 35(45), 1996, pp. 14312-14317
THE SPECIFIC CONTRIBUTION OF THE NOVEL ALPHA-1D ADRENOCEPTOR TO THE CONTRACTION OF VASCULAR SMOOTH-MUSCLE
Authors: PIASCIK MT GUARINO RD SMITH MS SOLTIS EE SAUSSY DL PEREZ DM
Citation: Mt. Piascik et al., THE SPECIFIC CONTRIBUTION OF THE NOVEL ALPHA-1D ADRENOCEPTOR TO THE CONTRACTION OF VASCULAR SMOOTH-MUSCLE, The Journal of pharmacology and experimental therapeutics, 275(3), 1995, pp. 1583-1589
SYNTHETIC AND STRUCTURE-ACTIVITY STUDIES ON ACID-SUBSTITUTED 2-ARYLPHENOLS - DISCOVERY OF OPHENYL)-5-HYDROXYPHENOXY]-PROPOXY]PHENOXY]BENZOIC ACID, A HIGH-AFFINITY LEUKOTRIENE B-4 RECEPTOR ANTAGONIST
Authors: SAWYER JS BACH NJ BAKER SR BALDWIN RF BORROMEO PS COCKERHAM SL FLEISCH JH FLOREANCIG P FROELICH LL JACKSON WT MARDER P PALKOWITZ JA ROMAN CR SAUSSY DL SCHMITTLING EA SILBAUGH SA SPAETHE SM STENGEL PW SOFIA MJ
Citation: Js. Sawyer et al., SYNTHETIC AND STRUCTURE-ACTIVITY STUDIES ON ACID-SUBSTITUTED 2-ARYLPHENOLS - DISCOVERY OF OPHENYL)-5-HYDROXYPHENOXY]-PROPOXY]PHENOXY]BENZOIC ACID, A HIGH-AFFINITY LEUKOTRIENE B-4 RECEPTOR ANTAGONIST, Journal of medicinal chemistry, 38(22), 1995, pp. 4411-4432
BMY-7378 IS A SELECTIVE ANTAGONIST OF THE D-SUBTYPE OF ALPHA(1)-ADRENOCEPTORS
Authors: GOETZ AS KING HK WARD SDC TRUE TA RIMELE TJ SAUSSY DL
Citation: As. Goetz et al., BMY-7378 IS A SELECTIVE ANTAGONIST OF THE D-SUBTYPE OF ALPHA(1)-ADRENOCEPTORS, European journal of pharmacology, 272(2-3), 1995, pp. 5-6
QSAR STUDY OF ORTHO-PHENYLPHENOL LEUKOTRIENE B4 RECEPTOR ANTAGONISTS
Authors: WIKEL JH SOFIA MJ SAUSSY DL BEMIS KG
Citation: Jh. Wikel et al., QSAR STUDY OF ORTHO-PHENYLPHENOL LEUKOTRIENE B4 RECEPTOR ANTAGONISTS, Bioorganic & medicinal chemistry letters, 4(6), 1994, pp. 795-800
STRUCTURAL ANALOGS OF LY292728, A HIGHLY POTENT XANTHONE DICARBOXYLIC-ACID LEUKOTRIENE B-4 RECEPTOR ANTAGONIST - SPATIAL POSITIONING OF THESECONDARY ACID GROUP
Authors: SAWYER JS SCHMITTLING EA BACH NJ BAKER SR FROELICH LL SAUSSY DL MARDER P JACKSON WT
Citation: Js. Sawyer et al., STRUCTURAL ANALOGS OF LY292728, A HIGHLY POTENT XANTHONE DICARBOXYLIC-ACID LEUKOTRIENE B-4 RECEPTOR ANTAGONIST - SPATIAL POSITIONING OF THESECONDARY ACID GROUP, Bioorganic & medicinal chemistry letters, 4(17), 1994, pp. 2077-2082
EFFECT OF ALKALINE-PHOSPHATASE ON THROMBOXANE MIMETIC INDUCED PLATELET ACTIVATION
Authors: MARGOLIN N TRUE TA SAUSSY DL MAIS DE
Citation: N. Margolin et al., EFFECT OF ALKALINE-PHOSPHATASE ON THROMBOXANE MIMETIC INDUCED PLATELET ACTIVATION, Prostaglandins, 48(4), 1994, pp. 235-246
CHARACTERIZATION OF ALPHA-1-ADRENOCEPTOR SUBTYPES IN HUMAN AND CANINEPROSTATE MEMBRANES
Authors: GOETZ AS LUTZ MW RIMELE TJ SAUSSY DL
Citation: As. Goetz et al., CHARACTERIZATION OF ALPHA-1-ADRENOCEPTOR SUBTYPES IN HUMAN AND CANINEPROSTATE MEMBRANES, The Journal of pharmacology and experimental therapeutics, 271(3), 1994, pp. 1228-1233
CHARACTERIZATION OF THROMBOXANE A(2) PROSTAGLANDIN H-2 BINDING-SITES IN GUINEA-PIG CARDIAC MEMBRANE PREPARATIONS
Authors: BOWLING N DUBE GP KURTZ WL BRUNE KA SAUSSY DL DORN GW MAIS DE
Citation: N. Bowling et al., CHARACTERIZATION OF THROMBOXANE A(2) PROSTAGLANDIN H-2 BINDING-SITES IN GUINEA-PIG CARDIAC MEMBRANE PREPARATIONS, Journal of Molecular and Cellular Cardiology, 26(7), 1994, pp. 915-923
ACID UNIT MODIFICATIONS OF 1,2,4,5-SUBSTITUTED HYDROXYACETOPHENONES AND THE EFFECT ON INVITRO AND INVIVO LTB(4) RECEPTOR ANTAGONISM
Authors: SOFIA MJ FLOREANCIG P JACKSON WT MARDER P SAUSSY DL SILBAUGH SA COCKERHAM SL FROELICH LL ROMAN CR STENGEL PW FLEISCH JH
Citation: Mj. Sofia et al., ACID UNIT MODIFICATIONS OF 1,2,4,5-SUBSTITUTED HYDROXYACETOPHENONES AND THE EFFECT ON INVITRO AND INVIVO LTB(4) RECEPTOR ANTAGONISM, Bioorganic & medicinal chemistry letters, 3(6), 1993, pp. 1147-1152
SYNTHESIS AND PHARMACOLOGICAL ACTIVITY OF HYDROXYACETOPHENONE-SUBSTITUTED BENZOPHENONE XANTHONE LEUKOTRIENE B-4 RECEPTOR ANTAGONISTS/
Authors: SAWYER JS BALDWIN RF FROELICH LL SAUSSY DL JACKSON WT
Citation: Js. Sawyer et al., SYNTHESIS AND PHARMACOLOGICAL ACTIVITY OF HYDROXYACETOPHENONE-SUBSTITUTED BENZOPHENONE XANTHONE LEUKOTRIENE B-4 RECEPTOR ANTAGONISTS/, Bioorganic & medicinal chemistry letters, 3(10), 1993, pp. 1981-1984
DIARYL ETHER CARBOXYLIC ACID-DERIVATIVES OF LY255283 - RECEPTOR ANTAGONISTS OF LEUKOTRIENE B-4/
Authors: SAWYER JS BALDWIN RF SAUSSY DL FROELICH LL JACKSON WT
Citation: Js. Sawyer et al., DIARYL ETHER CARBOXYLIC ACID-DERIVATIVES OF LY255283 - RECEPTOR ANTAGONISTS OF LEUKOTRIENE B-4/, Bioorganic & medicinal chemistry letters, 3(10), 1993, pp. 1985-1990
O-PHENYLPHENOLS - POTENT AND ORALLY-ACTIVE LEUKOTRIENE B-4 RECEPTOR ANTAGONISTS
Authors: SOFIA MJ FLOREANCIG P BACH NJ BAKER SR COCKERHAM SL FLEISCH JH FROELICH LL JACKSON WT MARDER P ROMAN CR SAUSSY DL SPAETHE SM STENGEL PW SILBAUGH SA
Citation: Mj. Sofia et al., O-PHENYLPHENOLS - POTENT AND ORALLY-ACTIVE LEUKOTRIENE B-4 RECEPTOR ANTAGONISTS, Journal of medicinal chemistry, 36(24), 1993, pp. 3978-3981
BIPHENYLYL-SUBSTITUTED XANTHONES - HIGHLY POTENT LEUKOTRIENE B-4 RECEPTOR ANTAGONISTS
Authors: SAWYER JS BALDWIN RF SOFIA MJ FLOREANCIG P MARDER P SAUSSY DL FROELICH LL SILBAUGH SA STENGEL PW COCKERHAM SL JACKSON WT
Citation: Js. Sawyer et al., BIPHENYLYL-SUBSTITUTED XANTHONES - HIGHLY POTENT LEUKOTRIENE B-4 RECEPTOR ANTAGONISTS, Journal of medicinal chemistry, 36(24), 1993, pp. 3982-3984
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