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Results: 1-24 |
Results: 24
THE GLUCOPYRANOSE RING - AN ELASTIC SWITCH DISABLED BY PERIODATE-OXIDATION
Authors: MARSZALEK PE OBERHAUSER AF PANG YP FERNANDEZ JM
Citation: Pe. Marszalek et al., THE GLUCOPYRANOSE RING - AN ELASTIC SWITCH DISABLED BY PERIODATE-OXIDATION, Molecular biology of the cell, 9, 1998, pp. 1148-1148
SUPERCOMPUTING-BASED DIMERIC ANALOG APPROACH FOR DRUG OPTIMIZATION
Authors: PANG YP BRIMIJOIN S
Citation: Yp. Pang et S. Brimijoin, SUPERCOMPUTING-BASED DIMERIC ANALOG APPROACH FOR DRUG OPTIMIZATION, Parallel computing, 24(9-10), 1998, pp. 1557-1566
COMPUTER-DESIGNED BIS-OXIMES TO REACTIVATE PHOSPHORYLATED ACETYLCHOLINESTERASE
Authors: BRIMIJOIN S KERN C PANG YP
Citation: S. Brimijoin et al., COMPUTER-DESIGNED BIS-OXIMES TO REACTIVATE PHOSPHORYLATED ACETYLCHOLINESTERASE, Journal of neurochemistry, 71, 1998, pp. 19-19
DOCKING STUDIES ON THE COMPLEXED AND UNCOMPLEXED FKBP12 STRUCTURES WITH BOUND AND UNBOUND LIGANDS - AN IMPLICATION OF A CONFORMATIONAL SELECTION MECHANISM FOR BINDING
Authors: PANG YP SILVA ND HAYDOCK C PRENDERGAST FG
Citation: Yp. Pang et al., DOCKING STUDIES ON THE COMPLEXED AND UNCOMPLEXED FKBP12 STRUCTURES WITH BOUND AND UNBOUND LIGANDS - AN IMPLICATION OF A CONFORMATIONAL SELECTION MECHANISM FOR BINDING, JOURNAL OF MOLECULAR MODELING, 3(7), 1997, pp. 240-248
STRUCTURE OF ACETYLCHOLINESTERASE COMPLEXED WITH THE NOOTROPIC ALKALOID, (-)-HUPERZINE-A
Authors: RAVES ML HAREL M PANG YP SILMAN I KOZIKOWSKI AP SUSSMAN JL
Citation: Ml. Raves et al., STRUCTURE OF ACETYLCHOLINESTERASE COMPLEXED WITH THE NOOTROPIC ALKALOID, (-)-HUPERZINE-A, Nature structural biology, 4(1), 1997, pp. 57-63
DESIGN, SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF ACTIVE PYRROLE BASED, NONPEPTIDIC ANALOGS OF NEUROTENSIN(8-13)
Authors: HONG F ZAIDI J PANG YP CUSACK B RICHELSON E
Citation: F. Hong et al., DESIGN, SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF ACTIVE PYRROLE BASED, NONPEPTIDIC ANALOGS OF NEUROTENSIN(8-13), Journal of the Chemical Society. Perkin transactions. I, (20), 1997, pp. 2997-3003
SYNTHESIS OF ALKYLENE LINKED BIS-THA AND ALKYLENE LINKED BENZYL-THA AS HIGHLY POTENT AND SELECTIVE INHIBITORS AND MOLECULAR PROBES OF ACETYLCHOLINESTERASE
Authors: PANG YP HONG F QUIRAM P JELACIC T BRIMIJOIN S
Citation: Yp. Pang et al., SYNTHESIS OF ALKYLENE LINKED BIS-THA AND ALKYLENE LINKED BENZYL-THA AS HIGHLY POTENT AND SELECTIVE INHIBITORS AND MOLECULAR PROBES OF ACETYLCHOLINESTERASE, Journal of the Chemical Society. Perkin transactions. I, (2), 1997, pp. 171-176
DESIGN, SYNTHESIS AND PHARMACOLOGICAL TEST OF A QUINOLINE BASED, NONPEPTIDIC ANALOG OF NEUROTENSIN(8-13)
Authors: HONG F PANG YP CUSACK B RICHELSON E
Citation: F. Hong et al., DESIGN, SYNTHESIS AND PHARMACOLOGICAL TEST OF A QUINOLINE BASED, NONPEPTIDIC ANALOG OF NEUROTENSIN(8-13), Journal of the Chemical Society. Perkin transactions. I, (14), 1997, pp. 2083-2088
BIS-OXIMES MODELED ON CRYSTAL-STRUCTURE ARE POTENT REACTIVATORS OF ACETYLCHOLINESTERASE AFTER ORGANOPHOSPHATE INHIBITION
Authors: BRIMIJOIN S JONES S PANG YP
Citation: S. Brimijoin et al., BIS-OXIMES MODELED ON CRYSTAL-STRUCTURE ARE POTENT REACTIVATORS OF ACETYLCHOLINESTERASE AFTER ORGANOPHOSPHATE INHIBITION, Journal of neurochemistry, 69, 1997, pp. 75-75
ANATOMY OF THE NEUROTENSIN RECEPTOR - A MODEL FOR DRUG DESIGN
Authors: CUSACK B PANG YP MCCORMICK D GROSHAN K RICHELSON E
Citation: B. Cusack et al., ANATOMY OF THE NEUROTENSIN RECEPTOR - A MODEL FOR DRUG DESIGN, Biological psychiatry, 41, 1997, pp. 176-176
HIGHLY POTENT, SELECTIVE, AND LOW-COST BIS-TETRAHYDROAMINACRINE INHIBITORS OF ACETYLCHOLINESTERASE - STEPS TOWARD NOVEL DRUGS FOR TREATING ALZHEIMERS-DISEASE
Authors: PANG YP QUIRAM P JELACIC T HONG F BRIMIJOIN S
Citation: Yp. Pang et al., HIGHLY POTENT, SELECTIVE, AND LOW-COST BIS-TETRAHYDROAMINACRINE INHIBITORS OF ACETYLCHOLINESTERASE - STEPS TOWARD NOVEL DRUGS FOR TREATING ALZHEIMERS-DISEASE, The Journal of biological chemistry, 271(39), 1996, pp. 23646-23649
CHIMERIC RAT HUMAN NEUROTENSIN RECEPTORS LOCALIZE A REGION OF THE RECEPTOR SENSITIVE TO BINDING OF A NOVEL, SPECIES-SPECIFIC PICOMOLAR AFFINITY PEPTIDE. (VOL 271, PG 15054, 1996)
Authors: CUSAK B GROSHAN K MCCORMICK DJ PANG YP PERRY R PHUNG CT SOUDER T RICHELSON E
Citation: B. Cusak et al., CHIMERIC RAT HUMAN NEUROTENSIN RECEPTORS LOCALIZE A REGION OF THE RECEPTOR SENSITIVE TO BINDING OF A NOVEL, SPECIES-SPECIFIC PICOMOLAR AFFINITY PEPTIDE. (VOL 271, PG 15054, 1996), The Journal of biological chemistry, 271(36), 1996, pp. 22280-22280
CHIMERIC RAT HUMAN NEUROTENSIN RECEPTORS LOCALIZE A REGION OF THE RECEPTOR SENSITIVE TO BINDING OF A NOVEL, SPECIES-SPECIFIC, PICOMOLAR AFFINITY PEPTIDE/
Authors: CUSACK B GROSHAN K MCCORMICK DJ PANG YP PERRY R PHUNG CT SOUDER T RICHELSON E
Citation: B. Cusack et al., CHIMERIC RAT HUMAN NEUROTENSIN RECEPTORS LOCALIZE A REGION OF THE RECEPTOR SENSITIVE TO BINDING OF A NOVEL, SPECIES-SPECIFIC, PICOMOLAR AFFINITY PEPTIDE/, The Journal of biological chemistry, 271(25), 1996, pp. 15054-15059
PROPOSED LIGAND-BINDING SITE OF THE TRANSMEMBRANE RECEPTOR FOR NEUROTENSIN(8-13)
Authors: PANG YP CUSACK B GROSHAN K RICHELSON E
Citation: Yp. Pang et al., PROPOSED LIGAND-BINDING SITE OF THE TRANSMEMBRANE RECEPTOR FOR NEUROTENSIN(8-13), The Journal of biological chemistry, 271(25), 1996, pp. 15060-15068
APPLICATIONS OF FREE-ENERGY DERIVATIVES TO ANALOG DESIGN
Authors: PANG YP KOLLMAN PA
Citation: Yp. Pang et Pa. Kollman, APPLICATIONS OF FREE-ENERGY DERIVATIVES TO ANALOG DESIGN, Perspectives in drug discovery and design, 3, 1995, pp. 106-122
SYNTHESIS OF PARTIAL NONPEPTIDIC PEPTIDE MIMETICS AS POTENTIAL NEUROTENSIN AGONISTS AND ANTAGONISTS
Authors: KOZIKOWSKI AP DODD DS ZAIDI J PANG YP CUSACK B RICHELSON E
Citation: Ap. Kozikowski et al., SYNTHESIS OF PARTIAL NONPEPTIDIC PEPTIDE MIMETICS AS POTENTIAL NEUROTENSIN AGONISTS AND ANTAGONISTS, Journal of the Chemical Society. Perkin transactions. I, (12), 1995, pp. 1615-1621
PHARMACOLOGICAL AND BIOCHEMICAL PROFILES OF UNIQUE NEUROTENSIN-8-13 ANALOGS EXHIBITING SPECIES SELECTIVITY, STEREOSELECTIVITY, AND SUPERAGONISM
Authors: CUSACK B MCCORMICK DJ PANG YP SOUDER T GARCIA R FAUQ A RICHELSON E
Citation: B. Cusack et al., PHARMACOLOGICAL AND BIOCHEMICAL PROFILES OF UNIQUE NEUROTENSIN-8-13 ANALOGS EXHIBITING SPECIES SELECTIVITY, STEREOSELECTIVITY, AND SUPERAGONISM, The Journal of biological chemistry, 270(31), 1995, pp. 18359-18366
IDENTIFICATION OF AMINO-ACID-RESIDUES INVOLVED IN THE BINDING OF HUPERZINE-A TO CHOLINESTERASES
Authors: SAXENA A QIAN NF KOVACH IM KOZIKOWSKI AP PANG YP VELLOM DC RADIC Z QUINN D TAYLOR P DOCTOR BP
Citation: A. Saxena et al., IDENTIFICATION OF AMINO-ACID-RESIDUES INVOLVED IN THE BINDING OF HUPERZINE-A TO CHOLINESTERASES, Protein science, 3(10), 1994, pp. 1770-1778
PREDICTION OF THE BINDING-SITES OF HUPERZINE-A IN ACETYLCHOLINESTERASE BY DOCKING STUDIES
Authors: PANG YP KOZIKOWSKI AP
Citation: Yp. Pang et Ap. Kozikowski, PREDICTION OF THE BINDING-SITES OF HUPERZINE-A IN ACETYLCHOLINESTERASE BY DOCKING STUDIES, Journal of computer-aided molecular design, 8(6), 1994, pp. 669-681
PREDICTION OF THE BINDING-SITE OF 4-[(5,6-DIMETHOXY-1-INDANON-2-YL)METHYL]PIPERIDINE IN ACETYLCHOLINESTERASE BY DOCKING STUDIES WITH THE SYSDOC PROGRAM
Authors: PANG YP KOZIKOWSKI AP
Citation: Yp. Pang et Ap. Kozikowski, PREDICTION OF THE BINDING-SITE OF 4-[(5,6-DIMETHOXY-1-INDANON-2-YL)METHYL]PIPERIDINE IN ACETYLCHOLINESTERASE BY DOCKING STUDIES WITH THE SYSDOC PROGRAM, Journal of computer-aided molecular design, 8(6), 1994, pp. 683-693
RATIONAL DESIGN OF NOVEL NEUROTENSIN MIMETICS - DISCOVERY OF A PHARMACOLOGICALLY UNPRECEDENTED AGENT EXHIBITING CONCENTRATION-DEPENDENT DUAL EFFECTS AS ANTAGONIST AND FULL AGONIST
Authors: PANG YP ZAIDI J KOZIKOWSKI AP CUSACK B RICHELSON E
Citation: Yp. Pang et al., RATIONAL DESIGN OF NOVEL NEUROTENSIN MIMETICS - DISCOVERY OF A PHARMACOLOGICALLY UNPRECEDENTED AGENT EXHIBITING CONCENTRATION-DEPENDENT DUAL EFFECTS AS ANTAGONIST AND FULL AGONIST, Journal of computer-aided molecular design, 8(4), 1994, pp. 433-440
SYSDOC PREDICTION OF LIGAND-BINDING TO FKBP12 - COMPARISON WITH SPECTROSCOPIC EXPERIMENTS
Authors: SILVA N PANG YP KOZIKOWSK A PRENDERGAST F
Citation: N. Silva et al., SYSDOC PREDICTION OF LIGAND-BINDING TO FKBP12 - COMPARISON WITH SPECTROSCOPIC EXPERIMENTS, Biophysical journal, 66(2), 1994, pp. 10000029-10000029
PHARMACOLOGICAL STUDIES ON NOVEL NEUROTENSIN MIMETICS - DISCOVERY OF A PHARMACOLOGICALLY UNIQUE AGENT EXHIBITING CONCENTRATION-DEPENDENT DUAL EFFECTS AS ANTAGONIST AND AGONIST
Authors: CUSACK B RICHELSON E PANG YP ZAIDI J KOZIKOWSKI AP
Citation: B. Cusack et al., PHARMACOLOGICAL STUDIES ON NOVEL NEUROTENSIN MIMETICS - DISCOVERY OF A PHARMACOLOGICALLY UNIQUE AGENT EXHIBITING CONCENTRATION-DEPENDENT DUAL EFFECTS AS ANTAGONIST AND AGONIST, Molecular pharmacology, 44(5), 1993, pp. 1036-1040
SYNTHESIS, MOLECULAR MODELING, 2-D NMR, AND BIOLOGICAL EVALUATION OF ILV MIMICS AS POTENTIAL MODULATORS OF PROTEIN-KINASE-C
Authors: KOZIKOWSKI AP MA D PANG YP SHUM P LIKIC V MISHRA PK MACURA S BASU A LAZO JS BALL RG
Citation: Ap. Kozikowski et al., SYNTHESIS, MOLECULAR MODELING, 2-D NMR, AND BIOLOGICAL EVALUATION OF ILV MIMICS AS POTENTIAL MODULATORS OF PROTEIN-KINASE-C, Journal of the American Chemical Society, 115(10), 1993, pp. 3957-3965
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