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Results: 1-25 | 26-50 | 51-73 |
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SYNTHETIC OLIGOMERS OF CONFORMATIONALLY RESTRICTED PEPTIDES AS MODELSFOR MEMBRANE CHANNELS
Authors: LEPLAWY MT KOCIOLEK K SLOMCZYNSKA U ZABROCKI J BEUSEN DD MARSHALL GR
Citation: Mt. Leplawy et al., SYNTHETIC OLIGOMERS OF CONFORMATIONALLY RESTRICTED PEPTIDES AS MODELSFOR MEMBRANE CHANNELS, Polish Journal of Chemistry, 68(5), 1994, pp. 969-974
ANODIC AMIDE OXIDATIONS - CONFORMATIONALLY RESTRICTED PEPTIDE BUILDING-BLOCKS FROM THE DIRECT OXIDATIONS OF DIPEPTIDES
Authors: CORNILLE F FOBIAN YM SLOMCZYNSKA U BEUSEN DD MARSHALL GR MOELLER KD
Citation: F. Cornille et al., ANODIC AMIDE OXIDATIONS - CONFORMATIONALLY RESTRICTED PEPTIDE BUILDING-BLOCKS FROM THE DIRECT OXIDATIONS OF DIPEPTIDES, Tetrahedron letters, 35(38), 1994, pp. 6989-6992
BIOLOGICAL PROPERTIES OF THE BENZODIAZEPINE AMIDINE DERIVATIVE L-740,093, A CHOLECYSTOKININ-B GASTRIN RECEPTOR ANTAGONIST WITH HIGH-AFFINITY IN-VITRO AND HIGH POTENCY IN-VIVO
Authors: PATEL S SMITH AJ CHAPMAN KL FLETCHER AE KEMP JA MARSHALL GR HARGREAVES RJ RYECROFT W IVERSEN LL IVERSEN SD BAKER R SHOWELL GA BOURRAIN S NEDUVELIL JG MATASSA VG FREEDMAN SB
Citation: S. Patel et al., BIOLOGICAL PROPERTIES OF THE BENZODIAZEPINE AMIDINE DERIVATIVE L-740,093, A CHOLECYSTOKININ-B GASTRIN RECEPTOR ANTAGONIST WITH HIGH-AFFINITY IN-VITRO AND HIGH POTENCY IN-VIVO, Molecular pharmacology, 46(5), 1994, pp. 943-948
HIGH-AFFINITY AND POTENT, WATER-SOLUBLE 5-AMINO-1,4-BENZODIAZEPINE CCK(B) GASTRIN RECEPTOR ANTAGONISTS CONTAINING A CATIONIC SOLUBILIZING GROUP
Authors: SHOWELL GA BOURRAIN S NEDUVELIL JG FLETCHER SR BAKER R WATT AP FLETCHER AE FREEDMAN SB KEMP JA MARSHALL GR PATEL S SMITH AJ MATASSA VG
Citation: Ga. Showell et al., HIGH-AFFINITY AND POTENT, WATER-SOLUBLE 5-AMINO-1,4-BENZODIAZEPINE CCK(B) GASTRIN RECEPTOR ANTAGONISTS CONTAINING A CATIONIC SOLUBILIZING GROUP, Journal of medicinal chemistry, 37(6), 1994, pp. 719-721
2ND-GENERATION BENZODIAZEPINE CCK-B ANTAGONISTS - DEVELOPMENT OF SUBNANOMOLAR ANALOGS WITH SELECTIVITY AND WATER SOLUBILITY
Authors: BOCK MG DIPARDO RM MELLIN EC NEWTON RC VEBER DF FREEDMAN SB SMITH AJ PATEL S KEMP JA MARSHALL GR FLETCHER AE CHAPMAN KL ANDERSON PS FREIDINGER RM
Citation: Mg. Bock et al., 2ND-GENERATION BENZODIAZEPINE CCK-B ANTAGONISTS - DEVELOPMENT OF SUBNANOMOLAR ANALOGS WITH SELECTIVITY AND WATER SOLUBILITY, Journal of medicinal chemistry, 37(6), 1994, pp. 722-724
3-DIMENSIONAL QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP OF HUMAN-IMMUNODEFICIENCY-VIRUS-(I) PROTEASE INHIBITORS .2. PREDICTIVE POWER USING LIMITED EXPLORATION OF ALTERNATE BINDING MODES
Authors: OPREA TI WALLER CL MARSHALL GR
Citation: Ti. Oprea et al., 3-DIMENSIONAL QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP OF HUMAN-IMMUNODEFICIENCY-VIRUS-(I) PROTEASE INHIBITORS .2. PREDICTIVE POWER USING LIMITED EXPLORATION OF ALTERNATE BINDING MODES, Journal of medicinal chemistry, 37(14), 1994, pp. 2206-2215
(ARYLMETHYL)-3-PHENYL-4-HYDROXYQUINOLIN-2(1H)-ONES AND 3'-(ARYLOXY)-3-PHENYL-4-HYDROXYQUINOLIN-2(1H)-ONES - ORALLY-ACTIVE ANTAGONISTS OF THE GLYCINE SITE ON THE NMDA RECEPTOR
Authors: KULAGOWSKI JJ BAKER R CURTIS NR LEESON PD MAWER IM MOSELEY AM RIDGILL MP ROWLEY M STANSFIELD I FOSTER AC GRIMWOOD S HILL RG KEMP JA MARSHALL GR SAYWELL KL TRICKLEBANK MD
Citation: Jj. Kulagowski et al., (ARYLMETHYL)-3-PHENYL-4-HYDROXYQUINOLIN-2(1H)-ONES AND 3'-(ARYLOXY)-3-PHENYL-4-HYDROXYQUINOLIN-2(1H)-ONES - ORALLY-ACTIVE ANTAGONISTS OF THE GLYCINE SITE ON THE NMDA RECEPTOR, Journal of medicinal chemistry, 37(10), 1994, pp. 1402-1405
ALPHA 3(10)-HELIX TRANSITIONS IN ALPHA-METHYLALANINE HOMOPEPTIDES - CONFORMATIONAL TRANSITION PATHWAY AND POTENTIAL OF MEAN FORCE/
Authors: HUSTON SE MARSHALL GR
Citation: Se. Huston et Gr. Marshall, ALPHA 3(10)-HELIX TRANSITIONS IN ALPHA-METHYLALANINE HOMOPEPTIDES - CONFORMATIONAL TRANSITION PATHWAY AND POTENTIAL OF MEAN FORCE/, Biopolymers, 34(1), 1994, pp. 75-90
CONFORMATIONAL-ANALYSIS OF 2 CYCLIC ANALOGS OF ANGIOTENSIN - IMPLICATIONS FOR THE BIOLOGICALLY-ACTIVE CONFORMATION
Authors: NIKIFOROVICH GV KAO JLF PLUCINSKA K ZHANG WJ MARSHALL GR
Citation: Gv. Nikiforovich et al., CONFORMATIONAL-ANALYSIS OF 2 CYCLIC ANALOGS OF ANGIOTENSIN - IMPLICATIONS FOR THE BIOLOGICALLY-ACTIVE CONFORMATION, Biochemistry, 33(12), 1994, pp. 3591-3598
SPLICE - A PROGRAM TO ASSEMBLE PARTIAL QUERY SOLUTIONS FROM 3-DIMENSIONAL DATABASE SEARCHES INTO NOVEL LIGANDS
Authors: HO CMW MARSHALL GR
Citation: Cmw. Ho et Gr. Marshall, SPLICE - A PROGRAM TO ASSEMBLE PARTIAL QUERY SOLUTIONS FROM 3-DIMENSIONAL DATABASE SEARCHES INTO NOVEL LIGANDS, Journal of computer-aided molecular design, 7(6), 1993, pp. 623-647
KINETICS OF INTERACTIONS BETWEEN DRUGS AND RECEPTORS - STOCHASTIC CONCEPTION
Authors: KLIMOV GP MARSHALL GR
Citation: Gp. Klimov et Gr. Marshall, KINETICS OF INTERACTIONS BETWEEN DRUGS AND RECEPTORS - STOCHASTIC CONCEPTION, Computers & mathematics with applications, 26(10), 1993, pp. 1-25
CONFORMATION-FUNCTION RELATIONSHIPS IN LHRH ANALOGS .1. CONFORMATIONSOF LHRH PEPTIDE BACKBONE
Authors: NIKIFOROVICH GV MARSHALL GR
Citation: Gv. Nikiforovich et Gr. Marshall, CONFORMATION-FUNCTION RELATIONSHIPS IN LHRH ANALOGS .1. CONFORMATIONSOF LHRH PEPTIDE BACKBONE, International journal of peptide & protein research, 42(2), 1993, pp. 171-180
CONFORMATION-FUNCTION RELATIONSHIPS IN LHRH ANALOGS .2. CONFORMATIONSOF LHRH PEPTIDE AGONISTS AND ANTAGONISTS
Authors: NIKIFOROVICH GV MARSHALL GR
Citation: Gv. Nikiforovich et Gr. Marshall, CONFORMATION-FUNCTION RELATIONSHIPS IN LHRH ANALOGS .2. CONFORMATIONSOF LHRH PEPTIDE AGONISTS AND ANTAGONISTS, International journal of peptide & protein research, 42(2), 1993, pp. 181-193
A HIERARCHICAL APPROACH TO PEPTIDOMIMETIC DESIGN
Authors: MARSHALL GR
Citation: Gr. Marshall, A HIERARCHICAL APPROACH TO PEPTIDOMIMETIC DESIGN, Tetrahedron, 49(17), 1993, pp. 3547-3558
3-DIMENSIONAL QSAR OF HUMAN-IMMUNODEFICIENCY-VIRUS-(I) PROTEASE INHIBITORS .1. A COMFA STUDY EMPLOYING EXPERIMENTALLY-DETERMINED ALIGNMENT RULES
Authors: WALLER CL OPREA TI GIOLITTI A MARSHALL GR
Citation: Cl. Waller et al., 3-DIMENSIONAL QSAR OF HUMAN-IMMUNODEFICIENCY-VIRUS-(I) PROTEASE INHIBITORS .1. A COMFA STUDY EMPLOYING EXPERIMENTALLY-DETERMINED ALIGNMENT RULES, Journal of medicinal chemistry, 36(26), 1993, pp. 4152-4160
3-ACYL-4-HYDROXYQUINOLIN-2(1H)-ONES - SYSTEMICALLY ACTIVE ANTICONVULSANTS ACTING BY ANTAGONISM AT THE GLYCINE SITE OF THE N-METHL-D-ASPARTATE RECEPTOR COMPLEX
Authors: ROWLEY M LEESON PD STEVENSON GI MOSELEY AM STANSFIELD I SANDERSON I ROBINSON L BAKER R KEMP JA MARSHALL GR FOSTER AC GRIMWOOD S TRICKLEBANK MD SAYWELL KL
Citation: M. Rowley et al., 3-ACYL-4-HYDROXYQUINOLIN-2(1H)-ONES - SYSTEMICALLY ACTIVE ANTICONVULSANTS ACTING BY ANTAGONISM AT THE GLYCINE SITE OF THE N-METHL-D-ASPARTATE RECEPTOR COMPLEX, Journal of medicinal chemistry, 36(22), 1993, pp. 3386-3396
3-NITRO-3,4-DIHYDRO-2(1H)-QUINOLONES - EXCITATORY AMINO-ACID ANTAGONISTS ACTING AT GLYCINE-SITE NMDA AND LPHA-AMINO-3-HYDROXY-5-METHYL-4-ISOXAZOLEPROPIONIC ACID RECEPTORS
Authors: CARLING RW LEESON PD MOORE KW SMITH JD MOYES CR MAWER IM THOMAS S CHAN T BAKER R FOSTER AC GRIMWOOD S KEMP JA MARSHALL GR TRICKLEBANK MD SAYWELL KL
Citation: Rw. Carling et al., 3-NITRO-3,4-DIHYDRO-2(1H)-QUINOLONES - EXCITATORY AMINO-ACID ANTAGONISTS ACTING AT GLYCINE-SITE NMDA AND LPHA-AMINO-3-HYDROXY-5-METHYL-4-ISOXAZOLEPROPIONIC ACID RECEPTORS, Journal of medicinal chemistry, 36(22), 1993, pp. 3397-3408
3-DIMENSIONAL QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP OF ANGIOTESIN-CONVERTING ENZYME AND THERMOLYSIN INHIBITORS .2. A COMPARISON OF COMFA MODELS INCORPORATING MOLECULAR-ORBITAL FIELDS AND DESOLVATION FREE-ENERGIES BASED ON ACTIVE-ANALOG AND COMPLEMENTARY-RECEPTOR-FIELD ALIGNMENT RULES
Authors: WALLER CL MARSHALL GR
Citation: Cl. Waller et Gr. Marshall, 3-DIMENSIONAL QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP OF ANGIOTESIN-CONVERTING ENZYME AND THERMOLYSIN INHIBITORS .2. A COMPARISON OF COMFA MODELS INCORPORATING MOLECULAR-ORBITAL FIELDS AND DESOLVATION FREE-ENERGIES BASED ON ACTIVE-ANALOG AND COMPLEMENTARY-RECEPTOR-FIELD ALIGNMENT RULES, Journal of medicinal chemistry, 36(16), 1993, pp. 2390-2403
MULTIPLE BINDING MODES FOR THE RECEPTOR-BOUND CONFORMATIONS OF CYCLICAII AGONISTS
Authors: PLUCINSKA K KATAOKA T YODO M CODY WL HE JX HUMBLET C LU GH LUNNEY E MAJOR TC PANEK RL SCHELKUN P SKEEAN R MARSHALL GR
Citation: K. Plucinska et al., MULTIPLE BINDING MODES FOR THE RECEPTOR-BOUND CONFORMATIONS OF CYCLICAII AGONISTS, Journal of medicinal chemistry, 36(13), 1993, pp. 1902-1913
EFFECTS OF ELECTRIC-FIELD ON ALAMETHICIN BOUND AT THE LIPID-WATER INTERFACE - A MOLECULAR MECHANICS STUDY
Authors: GALAKTIONOV SG MARSHALL GR
Citation: Sg. Galaktionov et Gr. Marshall, EFFECTS OF ELECTRIC-FIELD ON ALAMETHICIN BOUND AT THE LIPID-WATER INTERFACE - A MOLECULAR MECHANICS STUDY, Biophysical journal, 65(2), 1993, pp. 608-617
3-DIMENSIONAL RECOGNITION REQUIREMENTS FOR ANGIOTENSIN AGONISTS - A NOVEL SOLUTION FOR AN OLD PROBLEM
Authors: NIKIFOROVICH GV MARSHALL GR
Citation: Gv. Nikiforovich et Gr. Marshall, 3-DIMENSIONAL RECOGNITION REQUIREMENTS FOR ANGIOTENSIN AGONISTS - A NOVEL SOLUTION FOR AN OLD PROBLEM, Biochemical and biophysical research communications, 195(1), 1993, pp. 222-228
FREE-ENERGY PROFILE OF A 3(10)-HELICAL TO ALPHA-HELICAL TRANSITION OFAN OLIGOPEPTIDE IN VARIOUS SOLVENTS
Authors: SMYTHE ML HUSTON SE MARSHALL GR
Citation: Ml. Smythe et al., FREE-ENERGY PROFILE OF A 3(10)-HELICAL TO ALPHA-HELICAL TRANSITION OFAN OLIGOPEPTIDE IN VARIOUS SOLVENTS, Journal of the American Chemical Society, 115(24), 1993, pp. 11594-11595
3D-QSAR OF ANGIOTENSIN-CONVERTING ENZYME AND THERMOLYSIN INHIBITORS -A COMPARISON OF COMFA MODELS BASED ON DEDUCED AND EXPERIMENTALLY DETERMINED ACTIVE-SITE GEOMETRIES
Authors: DEPRIEST SA MAYER D NAYLOR CB MARSHALL GR
Citation: Sa. Depriest et al., 3D-QSAR OF ANGIOTENSIN-CONVERTING ENZYME AND THERMOLYSIN INHIBITORS -A COMPARISON OF COMFA MODELS BASED ON DEDUCED AND EXPERIMENTALLY DETERMINED ACTIVE-SITE GEOMETRIES, Journal of the American Chemical Society, 115(13), 1993, pp. 5372-5384
Risultati: 1-25 | 26-50 | 51-73 |