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Results: 1-10 |
Results: 10
QUINOLINE-SUBSTITUTED DIHYDROINDOLES AS CYSLT(1) (LTD(4) RECEPTOR) ANTAGONISTS
Authors: SAWYER JS THRASHER KJ BACH NJ STENGEL PW COCKERHAM SL SILBAUGH SA ROMAN CR FROELICH LL FLEISCH JH
Citation: Js. Sawyer et al., QUINOLINE-SUBSTITUTED DIHYDROINDOLES AS CYSLT(1) (LTD(4) RECEPTOR) ANTAGONISTS, Bioorganic & medicinal chemistry letters, 6(3), 1996, pp. 249-252
RECOMBINANT HUMAN SECRETORY PHOSPHOLIPASE A(2) RELEASED THROMBOXANE FROM GUINEA-PIG BRONCHOALVEOLAR LAVAGE CELLS - IN-VITRO AND EX-VIVO EVALUATION OF A NOVEL SECRETORY PHOSPHOLIPASE A(2) INHIBITOR
Authors: FLEISCH JH ARMSTRONG CT ROMAN CR MIHELICH ED SPAETHE SM JACKSON WT BOBBITT JL DRAHEIM S BACH NJ DILLARD RD MARTINELLI M FOUTS R SNYDER DW
Citation: Jh. Fleisch et al., RECOMBINANT HUMAN SECRETORY PHOSPHOLIPASE A(2) RELEASED THROMBOXANE FROM GUINEA-PIG BRONCHOALVEOLAR LAVAGE CELLS - IN-VITRO AND EX-VIVO EVALUATION OF A NOVEL SECRETORY PHOSPHOLIPASE A(2) INHIBITOR, The Journal of pharmacology and experimental therapeutics, 278(1), 1996, pp. 252-257
INDOLE INHIBITORS OF HUMAN NONPANCREATIC SECRETORY PHOSPHOLIPASE A(2).1. INDOLE-3-ACETAMIDES
Authors: DILLARD RD BACH NJ DRAHEIM SE BERRY DR CARLSON DG CHIRGADZE NY CLAWSON DK HARTLEY LW JOHNSON LM JONES ND MCKINNEY ER MIHELICH ED OLKOWSKI JL SCHEVITZ RW SMITH AC SNYDER DW SOMMERS CD WERY JP
Citation: Rd. Dillard et al., INDOLE INHIBITORS OF HUMAN NONPANCREATIC SECRETORY PHOSPHOLIPASE A(2).1. INDOLE-3-ACETAMIDES, Journal of medicinal chemistry, 39(26), 1996, pp. 5119-5136
INDOLE INHIBITORS OF HUMAN NONPANCREATIC SECRETORY PHOSPHOLIPASE A(2).2. INDOLE-3-ACETAMIDES WITH ADDITIONAL FUNCTIONALITY
Authors: DILLARD RD BACH NJ DRAHEIM SE BERRY DR CARLSON DG CHIRGADZE NY CLAWSON DK HARTLEY LW JOHNSON LM JONES ND MCKINNEY ER MIHELICH ED OLKOWSKI JL SCHEVITZ RW SMITH AC SNYDER DW SOMMERS CD WERY JP
Citation: Rd. Dillard et al., INDOLE INHIBITORS OF HUMAN NONPANCREATIC SECRETORY PHOSPHOLIPASE A(2).2. INDOLE-3-ACETAMIDES WITH ADDITIONAL FUNCTIONALITY, Journal of medicinal chemistry, 39(26), 1996, pp. 5137-5158
INDOLE INHIBITORS OF HUMAN NONPANCREATIC SECRETORY PHOSPHOLIPASE A(2).3. INDOLE-3-GLYOXAMIDES
Authors: DRAHEIM SE BACH NJ DILLARD RD BERRY DR CARLSON DG CHIRGADZE NY CLAWSON DK HARTLEY LW JOHNSON LM JONES ND MCKINNEY ER MIHELICH ED OLKOWSKI JL SCHEVITZ RW SMITH AC SNYDER DW SOMMERS CD WERY JP
Citation: Se. Draheim et al., INDOLE INHIBITORS OF HUMAN NONPANCREATIC SECRETORY PHOSPHOLIPASE A(2).3. INDOLE-3-GLYOXAMIDES, Journal of medicinal chemistry, 39(26), 1996, pp. 5159-5175
TRANSGENIC MODEL FOR THE DISCOVERY OF NOVEL HUMAN SECRETORY NONPANCREATIC PHOSPHOLIPASE A(2) INHIBITORS
Authors: FOX N SONG M SCHREMENTI J SHARP JD WHITE DL SNYDER DW HARTLEY LW CARLSON DG BACH NJ DILLARD RD DRAHEIM SE BOBBITT JL FISHER L MIHELICH ED
Citation: N. Fox et al., TRANSGENIC MODEL FOR THE DISCOVERY OF NOVEL HUMAN SECRETORY NONPANCREATIC PHOSPHOLIPASE A(2) INHIBITORS, European journal of pharmacology, 308(2), 1996, pp. 195-203
STRUCTURE-BASED DESIGN OF THE FIRST POTENT AND SELECTIVE INHIBITOR OFHUMAN NONPANCREATIC SECRETORY PHOSPHOLIPASE-A(2)
Authors: SCHEVITZ RW BACH NJ CARLSON DG CHIRGADZE NY CLAWSON DK DILLARD RD DRAHEIM SE HARTLEY LW JONES ND MIHELICH ED OLKOWSKI JL SNYDER DW SOMMERS C WERY JP
Citation: Rw. Schevitz et al., STRUCTURE-BASED DESIGN OF THE FIRST POTENT AND SELECTIVE INHIBITOR OFHUMAN NONPANCREATIC SECRETORY PHOSPHOLIPASE-A(2), Nature structural biology, 2(6), 1995, pp. 458-465
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
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
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
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