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Results: 1-17 |
Results: 17
MOLECULAR MODELING
Authors: BROUGHTON HB
Citation: Hb. Broughton, MOLECULAR MODELING, CURRENT OPINION IN CHEMICAL BIOLOGY, 1(3), 1997, pp. 392-398
BIOACTIVE ISOXAZOLINE AND OXIME DERIVATIVES FROM 7-KETOLIGNANS
Authors: DELCORRAL JMM GORDALIZA M CASTRO MA LOPEZVAZQUEZ ML GARCIAGRAVALOS MD BROUGHTON HB SANFELICIANO A
Citation: Jmm. Delcorral et al., BIOACTIVE ISOXAZOLINE AND OXIME DERIVATIVES FROM 7-KETOLIGNANS, Tetrahedron, 53(18), 1997, pp. 6555-6564
5-(PIPERIDIN-2-YL)-1,4-BENZODIAZEPINES AND 5-(HOMOPIPERIDIN-2-YL)-1,4-BENZODIAZEPINES - HIGH-AFFINITY, BASIC LIGANDS FOR THE CHOLECYSTOKININ-B RECEPTOR
Authors: CASTRO JL BROUGHTON HB RUSSELL MGN RATHBONE D WATT AP BALL RG CHAPMAN KL PATEL S SMITH AJ MARSHALL GR MATASSA VG
Citation: Jl. Castro et al., 5-(PIPERIDIN-2-YL)-1,4-BENZODIAZEPINES AND 5-(HOMOPIPERIDIN-2-YL)-1,4-BENZODIAZEPINES - HIGH-AFFINITY, BASIC LIGANDS FOR THE CHOLECYSTOKININ-B RECEPTOR, Journal of medicinal chemistry, 40(16), 1997, pp. 2491-2501
4-HETEROCYCLYLPIPERIDINES AS SELECTIVE HIGH-AFFINITY LIGANDS AT THE HUMAN DOPAMINE D4 RECEPTOR
Authors: ROWLEY M COLLINS I BROUGHTON HB DAVEY WB BAKER R EMMS F MARWOOD R PATEL S PATEL S RAGAN CI FREEDMAN SB BALL R LEESON PD
Citation: M. Rowley et al., 4-HETEROCYCLYLPIPERIDINES AS SELECTIVE HIGH-AFFINITY LIGANDS AT THE HUMAN DOPAMINE D4 RECEPTOR, Journal of medicinal chemistry, 40(15), 1997, pp. 2374-2385
THE CHEMICAL EVOLUTION OF 2-[5-(1,2,4-TRIAZOL-4-YL)-1H-INDOL-3-YL]ETHYLAMINE (L-741,604) AND ANALOGS - POTENT AND SELECTIVE AGONISTS FOR 5-HT1D RECEPTORS
Authors: STERNFELD F BAKER R BROUGHTON HB GUIBLIN AR JELLEY RA MATASSA VG REEVE AJ BEER MS STANTON JA HARGREAVES RJ SHEPHEARD SL LONGMORE J RAZZAQUE Z GRAHAM MI SOHAL B STREET LJ
Citation: F. Sternfeld et al., THE CHEMICAL EVOLUTION OF 2-[5-(1,2,4-TRIAZOL-4-YL)-1H-INDOL-3-YL]ETHYLAMINE (L-741,604) AND ANALOGS - POTENT AND SELECTIVE AGONISTS FOR 5-HT1D RECEPTORS, Bioorganic & medicinal chemistry letters, 6(15), 1996, pp. 1825-1830
CONTROLLED MODIFICATION OF ACIDITY IN CHOLECYSTOKININ B RECEPTOR ANTAGONISTS - ZEPIN-3-YL)-N'-[3-(TETRAZOL-5-YLAMINO)PHENYL]UREAS
Authors: CASTRO JL BALL RG BROUGHTON HB RUSSELL MGN RATHBONE D WATT AP BAKER R CHAPMAN KL FLETCHER AE PATEL S SMITH AJ MARSHALL GR RYECROFT W MATASSA VG
Citation: Jl. Castro et al., CONTROLLED MODIFICATION OF ACIDITY IN CHOLECYSTOKININ B RECEPTOR ANTAGONISTS - ZEPIN-3-YL)-N'-[3-(TETRAZOL-5-YLAMINO)PHENYL]UREAS, Journal of medicinal chemistry, 39(4), 1996, pp. 842-849
L)PIPERAZIN-1-YL]METHYL]-1H-PYRROLO[2,3-B]PYRIDINE - AN ANTAGONIST WITH HIGH-AFFINITY AND SELECTIVITY FOR THE HUMAN DOPAMINE D-4 RECEPTOR
Authors: KULAGOWSKI JJ BROUGHTON HB CURTIS NR MAWER IM RIDGILL MP BAKER R EMMS F FREEDMAN SB MARWOOD R PATEL S PATEL S RAGAN CI LEESON PD
Citation: Jj. Kulagowski et al., L)PIPERAZIN-1-YL]METHYL]-1H-PYRROLO[2,3-B]PYRIDINE - AN ANTAGONIST WITH HIGH-AFFINITY AND SELECTIVITY FOR THE HUMAN DOPAMINE D-4 RECEPTOR, Journal of medicinal chemistry, 39(10), 1996, pp. 1941-1942
ETHYL-3-(1-(2-PHENYLETHYL)PIPERIDIN-4-YL)ISOXAZOLE - A POTENT, SELECTIVE ANTAGONIST AT HUMAN CLONED DOPAMINE D4 RECEPTORS
Authors: ROWLEY M BROUGHTON HB COLLINS I BAKER R EMMS F MARWOOD R PATEL S PATEL S RAGAN CI FREEDMAN SB LEESON PD
Citation: M. Rowley et al., ETHYL-3-(1-(2-PHENYLETHYL)PIPERIDIN-4-YL)ISOXAZOLE - A POTENT, SELECTIVE ANTAGONIST AT HUMAN CLONED DOPAMINE D4 RECEPTORS, Journal of medicinal chemistry, 39(10), 1996, pp. 1943-1945
STUDIES OF IMIDAZOLE AND PYRAZOLE PROTONATION USING ELECTROSTATICALLYTRAINED NEURAL NETWORKS
Authors: BROUGHTON HB GREEN SM RZEPA HS
Citation: Hb. Broughton et al., STUDIES OF IMIDAZOLE AND PYRAZOLE PROTONATION USING ELECTROSTATICALLYTRAINED NEURAL NETWORKS, Perkin transactions. 2, (3), 1995, pp. 431-435
INOSITOL MONOPHOSPHATASE - A PUTATIVE TARGET FOR LI+ IN THE TREATMENTOF BIPOLAR DISORDER
Authors: ATACK JR BROUGHTON HB POLLACK SJ
Citation: Jr. Atack et al., INOSITOL MONOPHOSPHATASE - A PUTATIVE TARGET FOR LI+ IN THE TREATMENTOF BIPOLAR DISORDER, Trends in neurosciences, 18(8), 1995, pp. 343-349
STRUCTURE ACID MECHANISM OF INOSITOL MONOPHOSPHATASE
Authors: ATACK JR BROUGHTON HB POLLACK SJ
Citation: Jr. Atack et al., STRUCTURE ACID MECHANISM OF INOSITOL MONOPHOSPHATASE, FEBS letters, 361(1), 1995, pp. 1-7
SYNTHESIS AND SEROTONERGIC ACTIVITY OF BENZOFURAN AND DIHYDROBENZOFURAN ANALOGS OF 5-CARBOXAMIDOTRYPTAMINE
Authors: RUSSELL MGN CASTRO JL MATASSA VG BEER MS HEALD A SCHOLEY K STANTON JA BROUGHTON HB
Citation: Mgn. Russell et al., SYNTHESIS AND SEROTONERGIC ACTIVITY OF BENZOFURAN AND DIHYDROBENZOFURAN ANALOGS OF 5-CARBOXAMIDOTRYPTAMINE, Bioorganic & medicinal chemistry letters, 4(10), 1994, pp. 1207-1212
MECHANISM OF INOSITOL MONOPHOSPHATASE, THE PUTATIVE TARGET OF LITHIUM-THERAPY
Authors: POLLACK SJ ATACK JR KNOWLES MR MCALLISTER G RAGAN CI BAKER R FLETCHER SR IVERSEN LL BROUGHTON HB
Citation: Sj. Pollack et al., MECHANISM OF INOSITOL MONOPHOSPHATASE, THE PUTATIVE TARGET OF LITHIUM-THERAPY, Proceedings of the National Academy of Sciences of the United Statesof America, 91(13), 1994, pp. 5766-5770
STRUCTURAL-ANALYSIS OF INOSITOL MONOPHOSPHATASE COMPLEXES WITH SUBSTRATES
Authors: BONE R FRANK L SPRINGER JP POLLACK SJ OSBORNE S ATACK JR KNOWLES MR MCALLISTER G RAGAN CI BROUGHTON HB BAKER R FLETCHER SR
Citation: R. Bone et al., STRUCTURAL-ANALYSIS OF INOSITOL MONOPHOSPHATASE COMPLEXES WITH SUBSTRATES, Biochemistry, 33(32), 1994, pp. 9460-9467
2-NAP - A SELECTIVE, HYDROPHILIC, NONPEPTIDE CCKA-RECEPTOR ANTAGONISTDERIVED FROM THE CHOLECYSTOKININ C-TERMINAL DIPEPTIDE
Authors: MCDONALD IM BODKIN MJ BROUGHTON HB DUNSTONE DJ KALINDJIAN SB LOW CMR
Citation: Im. Mcdonald et al., 2-NAP - A SELECTIVE, HYDROPHILIC, NONPEPTIDE CCKA-RECEPTOR ANTAGONISTDERIVED FROM THE CHOLECYSTOKININ C-TERMINAL DIPEPTIDE, Bioorganic & medicinal chemistry letters, 3(8), 1993, pp. 1511-1516
SYNTHESIS, BIOLOGICAL-ACTIVITY AND ELECTROSTATIC PROPERTIES OF [(3-AMINO-1,2,4-THIADIAZOL-5-YL)METHYL]-1H-INDOLE, A NOVEL 5-HT1D RECEPTOR AGONIST
Authors: CASTRO JL MATASSA VG BROUGHTON HB MOSLEY RT STREET LJ BAKER R
Citation: Jl. Castro et al., SYNTHESIS, BIOLOGICAL-ACTIVITY AND ELECTROSTATIC PROPERTIES OF [(3-AMINO-1,2,4-THIADIAZOL-5-YL)METHYL]-1H-INDOLE, A NOVEL 5-HT1D RECEPTOR AGONIST, Bioorganic & medicinal chemistry letters, 3(6), 1993, pp. 993-997
PROBING THE ROLE OF METAL-IONS IN THE MECHANISM OF INOSITOL MONOPHOSPHATASE BY SITE-DIRECTED MUTAGENESIS
Authors: POLLACK SJ KNOWLES MR ATACK JR BROUGHTON HB RAGAN CI OSBORNE SA MCALLISTER G
Citation: Sj. Pollack et al., PROBING THE ROLE OF METAL-IONS IN THE MECHANISM OF INOSITOL MONOPHOSPHATASE BY SITE-DIRECTED MUTAGENESIS, European journal of biochemistry, 217(1), 1993, pp. 281-287
Risultati: 1-17 |