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Results: 1-18 |
Results: 18
NOVEL TERPHENYLS AS SELECTIVE CYCLOOXYGENASE-2 INHIBITORS AND ORALLY-ACTIVE ANTIINFLAMMATORY AGENTS
Authors: LI JJ NORTON MB REINHARD EJ ANDERSON GD GREGORY SA ISAKSON PC KOBOLDT CM MASFERRER JL PERKINS WE SEIBERT K ZHANG Y ZWEIFEL BS REITZ DB
Citation: Jj. Li et al., NOVEL TERPHENYLS AS SELECTIVE CYCLOOXYGENASE-2 INHIBITORS AND ORALLY-ACTIVE ANTIINFLAMMATORY AGENTS, Journal of medicinal chemistry, 39(9), 1996, pp. 1846-1856
DIARYLSPIRO[2.4]HEPTENES AS ORALLY-ACTIVE, HIGHLY SELECTIVE CYCLOOXYGENASE-2 INHIBITORS - SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS
Authors: HUANG HC LI JJ GARLAND DJ CHAMBERLAIN TS REINHARD EJ MANNING RE SEIBERT K KOBOLDT CM GREGORY SA ANDERSON GD VEENHUIZEN AW ZHANG Y PERKINS WE BURTON EG COGBURN JN ISAKSON PC REITZ DB
Citation: Hc. Huang et al., DIARYLSPIRO[2.4]HEPTENES AS ORALLY-ACTIVE, HIGHLY SELECTIVE CYCLOOXYGENASE-2 INHIBITORS - SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS, Journal of medicinal chemistry, 39(1), 1996, pp. 253-266
SELECTIVE CYCLOOXYGENASE INHIBITORS - NOVEL 4-SPIRO 1,2-DIARYLCYCLOPENTENES ARE POTENT AND ORALLY-ACTIVE COX-2 INHIBITORS
Authors: REITZ DB HUANG HC LI JJ GARLAND DJ MANNING RE ANDERSON GD GREGORY SA KOBOLDT CM PERKINS WE SEIBERT K ISAKSON PC
Citation: Db. Reitz et al., SELECTIVE CYCLOOXYGENASE INHIBITORS - NOVEL 4-SPIRO 1,2-DIARYLCYCLOPENTENES ARE POTENT AND ORALLY-ACTIVE COX-2 INHIBITORS, Bioorganic & medicinal chemistry letters, 5(8), 1995, pp. 867-872
DIARYL INDENES AND BENZOFURANS - NOVEL CLASSES OF POTENT AND SELECTIVE CYCLOOXYGENASE-2 INHIBITORS
Authors: HUANG HC CHAMBERLAIN TS SEIBERT K KOBOLDT CM ISAKSON PC REITZ DB
Citation: Hc. Huang et al., DIARYL INDENES AND BENZOFURANS - NOVEL CLASSES OF POTENT AND SELECTIVE CYCLOOXYGENASE-2 INHIBITORS, Bioorganic & medicinal chemistry letters, 5(20), 1995, pp. 2377-2380
ELUCIDATION OF THE INSURMOUNTABLE NATURE OF AN ANGIOTENSIN RECEPTOR ANTAGONIST, SC-54629
Authors: OLINS GM CHEN ST MCMAHON EG PALOMO MA REITZ DB
Citation: Gm. Olins et al., ELUCIDATION OF THE INSURMOUNTABLE NATURE OF AN ANGIOTENSIN RECEPTOR ANTAGONIST, SC-54629, Molecular pharmacology, 47(1), 1995, pp. 115-120
1,2-DIARYLCYCLOPENTENES AS SELECTIVE CYCLOOXYGENASE-2 INHIBITORS AND ORALLY-ACTIVE ANTIINFLAMMATORY AGENTS
Authors: LI JJ ANDERSON GD BURTON EG COGBURN JN COLLINS JT GARLAND DJ GREGORY SA HUANG HC ISAKSON PC KOBOLDT CM LOGUSCH EW NORTON MB PERKINS WE REINHARD EJ SEIBERT K VEENHUIZEN AW ZHANG Y REITZ DB
Citation: Jj. Li et al., 1,2-DIARYLCYCLOPENTENES AS SELECTIVE CYCLOOXYGENASE-2 INHIBITORS AND ORALLY-ACTIVE ANTIINFLAMMATORY AGENTS, Journal of medicinal chemistry, 38(22), 1995, pp. 4570-4578
1H-1,2,4-TRIAZOLE ANGIOTENSIN-II RECEPTOR ANTAGONISTS - N-PHENYLPYRIDINYLMETHYL AND N-PYRIDINYLPHENYLMETHYL ANALOGS OF SC-50560
Authors: REITZ DB PENICK MA REINHARD EJ CHENG BK OLINS GM CORPUS VM PALOMO MA MCGRAW DE MCMAHON EG
Citation: Db. Reitz et al., 1H-1,2,4-TRIAZOLE ANGIOTENSIN-II RECEPTOR ANTAGONISTS - N-PHENYLPYRIDINYLMETHYL AND N-PYRIDINYLPHENYLMETHYL ANALOGS OF SC-50560, Bioorganic & medicinal chemistry letters, 4(1), 1994, pp. 99-104
1H-1,2,4-TRIAZOLE ANGIOTENSIN-II RECEPTOR ANTAGONISTS - C-LINKED ANALOGS OF SC-50560
Authors: REITZ DB PENICK MA NORTON MB REINHARD EJ OLINS GM CORPUS VM PALOMO MA MCGRAW DE MCMAHON EG
Citation: Db. Reitz et al., 1H-1,2,4-TRIAZOLE ANGIOTENSIN-II RECEPTOR ANTAGONISTS - C-LINKED ANALOGS OF SC-50560, Bioorganic & medicinal chemistry letters, 4(1), 1994, pp. 105-110
N-1-STERICALLY HINDERED 2H-IMIDAZOL-2-ONE ANGIOTENSIN-II RECEPTOR ANTAGONISTS - THE SYNTHESIS OF [H-3] SC-54628 AND [H-3] SC-54629
Authors: REITZ DB GARLAND DJ OLINS GM MARKOS CS GRESK CJ LITSCHGI JW MCKINNIS BR
Citation: Db. Reitz et al., N-1-STERICALLY HINDERED 2H-IMIDAZOL-2-ONE ANGIOTENSIN-II RECEPTOR ANTAGONISTS - THE SYNTHESIS OF [H-3] SC-54628 AND [H-3] SC-54629, Bioorganic & medicinal chemistry letters, 4(1), 1994, pp. 111-114
ELUCIDATION OF THE INSURMOUNTABLE NATURE OF AN ANGIOTENSIN RECEPTOR ANTAGONIST
Authors: OLINS GM CHEN ST MCMAHON EG PALOMO MA REITZ DB
Citation: Gm. Olins et al., ELUCIDATION OF THE INSURMOUNTABLE NATURE OF AN ANGIOTENSIN RECEPTOR ANTAGONIST, The FASEB journal, 8(5), 1994, pp. 10000879-10000879
THE N-BOC GROUP AS AN ACTIVATOR FOR THE ALPHA-LITHIATION OF CARBAMATES - SYNTHESIS OF 11-SUBSTITUTED DIBENZOXAZEPINES
Authors: HAGEN TJ RAFFERTY MF COLLINS JT GARLAND DJ LI JJ NORTON MB REITZ DB TSYMBALOV S PITZELE BS HALLINAN EA
Citation: Tj. Hagen et al., THE N-BOC GROUP AS AN ACTIVATOR FOR THE ALPHA-LITHIATION OF CARBAMATES - SYNTHESIS OF 11-SUBSTITUTED DIBENZOXAZEPINES, Heterocycles, 38(3), 1994, pp. 601-611
A NOVEL ONE-POT CONVERSION OF METHYL SULFONES TO SULFONAMIDES
Authors: HUANG HC REINHARD EJ REITZ DB
Citation: Hc. Huang et al., A NOVEL ONE-POT CONVERSION OF METHYL SULFONES TO SULFONAMIDES, Tetrahedron letters, 35(39), 1994, pp. 7201-7204
SELECTIVE CYCLOOXYGENASE INHIBITORS - NOVEL 1,2-DIARYLCYCLOPENTENES ARE POTENT AND ORALLY-ACTIVE COX-2 INHIBITORS
Authors: REITZ DB LI JJ NORTON MB REINHARD EJ COLLINS JT ANDERSON GD GREGORY SA KOBOLDT CM PERKINS WE SEIBERT K ISAKSON PC
Citation: Db. Reitz et al., SELECTIVE CYCLOOXYGENASE INHIBITORS - NOVEL 1,2-DIARYLCYCLOPENTENES ARE POTENT AND ORALLY-ACTIVE COX-2 INHIBITORS, Journal of medicinal chemistry, 37(23), 1994, pp. 3878-3881
LITHIATION AND ELECTROPHILIC SUBSTITUTION OF ODIBENZ[B,F][1,4]-OXAZEPINE-10-TERT-BUTYLCARBAMATE - THE PREPARATION OF NOVEL FUSED HETEROCYCLIC-DERIVATIVES OF 8-CHLORODIBENZOXAZEPINE
Authors: LI JJ HAGEN TJ CHRUSCIEL RA NORTON MB TSYMBALOV S HALLINAN EA REITZ DB
Citation: Jj. Li et al., LITHIATION AND ELECTROPHILIC SUBSTITUTION OF ODIBENZ[B,F][1,4]-OXAZEPINE-10-TERT-BUTYLCARBAMATE - THE PREPARATION OF NOVEL FUSED HETEROCYCLIC-DERIVATIVES OF 8-CHLORODIBENZOXAZEPINE, Journal of heterocyclic chemistry, 31(6), 1994, pp. 1689-1696
N(1)-STERICALLY HINDERED 2H-IMIDAZOL-2-ONE ANGIOTENSIN-II RECEPTOR ANTAGONISTS - THE CONVERSION OF SURMOUNTABLE ANTAGONISTS TO INSURMOUNTABLE ANTAGONISTS
Authors: REITZ DB GARLAND DJ NORTON MB COLLINS JT REINHARD EJ MANNING RE OLINS GM CHEN ST PALOMO MA MCMAHON EG KOEHLER KF
Citation: Db. Reitz et al., N(1)-STERICALLY HINDERED 2H-IMIDAZOL-2-ONE ANGIOTENSIN-II RECEPTOR ANTAGONISTS - THE CONVERSION OF SURMOUNTABLE ANTAGONISTS TO INSURMOUNTABLE ANTAGONISTS, Bioorganic & medicinal chemistry letters, 3(6), 1993, pp. 1055-1060
IN-VIVO PHARMACOLOGY OF SC-51316, A NONPEPTIDIC ANGIOTENSIN-II RECEPTOR ANTAGONIST
Authors: OLINS GM SMITS GJ KOEPKE JP HUANG HC REITZ DB MANNING RE BLAINE EH
Citation: Gm. Olins et al., IN-VIVO PHARMACOLOGY OF SC-51316, A NONPEPTIDIC ANGIOTENSIN-II RECEPTOR ANTAGONIST, American journal of hypertension, 6(7), 1993, pp. 619-625
PHARMACOLOGY OF SC-52458, AN ORALLY-ACTIVE, NONPEPTIDE ANGIOTENSIN-AT(1) RECEPTOR ANTAGONIST
Authors: OLINS GM CORPUS VM CHEN ST MCMAHON EG PALOMO MA MCGRAW DE SMITS GJ NULL CL BROWN MA BITTNER SE KOEPKE JP BLEHM DJ SCHUH JR BAIERL CJ SCHMIDT RE COOK CS REITZ DB PENICK MA MANNING RE BLAINE EH
Citation: Gm. Olins et al., PHARMACOLOGY OF SC-52458, AN ORALLY-ACTIVE, NONPEPTIDE ANGIOTENSIN-AT(1) RECEPTOR ANTAGONIST, Journal of cardiovascular pharmacology, 22(4), 1993, pp. 617-625
SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF NONPEPTIDE, POTENT TRIAZOLONE-BASED ANGIOTENSIN-II RECEPTOR ANTAGONISTS
Authors: HUANG HC REITZ DB CHAMBERLAIN TS OLINS GM CORPUS VM MCMAHON EG PALOMO MA KOEPKE JP SMITS GJ MCGRAW DE BLAINE EH MANNING RE
Citation: Hc. Huang et al., SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF NONPEPTIDE, POTENT TRIAZOLONE-BASED ANGIOTENSIN-II RECEPTOR ANTAGONISTS, Journal of medicinal chemistry, 36(15), 1993, pp. 2172-2181
Risultati: 1-18 |