Research Topics
Genomes and Genes | E M ParkerSummaryAffiliation: Schering-Plough Research Institute Country: USA Publications
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Detail Information
Publications
GR231118 (1229U91) and other analogues of the C-terminus of neuropeptide Y are potent neuropeptide Y Y1 receptor antagonists and neuropeptide Y Y4 receptor agonistsE M Parker
Department of Central Nervous System and Cardiovascular Research, Schering Plough Research Institute, Kenilworth, NJ 07033 0539, USA
Eur J Pharmacol 349:97-105. 1998....
Neuropeptide Y receptors as targets for anti-obesity drug development: perspective and current statusEric Parker
Department of CNS and Cardiovascular Research, Schering Plough Research Institute, Mail Stop K 15 2 2760, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA
Eur J Pharmacol 440:173-87. 2002....
[D-Trp(34)] neuropeptide Y is a potent and selective neuropeptide Y Y(5) receptor agonist with dramatic effects on food intakeE M Parker
Department of CNS and Cardiovascular Research, Schering Plough Research Institute, Kenilworth, NJ 07033, USA
Peptides 21:393-9. 2000..These data demonstrate that [D-Trp(34)]NPY is a useful tool for studies aimed at determining the physiological roles of the NPY Y(5) receptor...
Rapamycin, but not FK506 and GPI-1046, increases neurite outgrowth in PC12 cells by inhibiting cell cycle progressionE M Parker
Department of CNS and Cardiovascular Research, Mail Stop K 15 3 3600, Schering Plough Research Institute, 2015 Galloping Hill Road, NJ 07033, Kenilworth, USA
Neuropharmacology 39:1913-9. 2000..The neuroprotective effect of FK506 and rapamycin against cerebral ischemia is probably not due to differentiation of neuronal precursors or stimulation of neuronal regeneration...
Activation of the NPY Y5 receptor regulates both feeding and energy expenditureJ J Hwa
Department of CNS, Schering Plough Research Institute, Kenilworth, New Jersey 07033, USA
Am J Physiol 277:R1428-34. 1999..These data suggest that the NPY Y5-receptor subtype not only mediates the feeding response of NPY but also contributes to brown fat temperature and energy expenditure regulation...
Potent pyrrolidine- and piperidine-based BACE-1 inhibitorsU Iserloh
Department of Chemical Research, Schering Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA
Bioorg Med Chem Lett 18:414-7. 2008..Extensive SAR studies on both pyrrolidines and piperidines ultimately led to inhibitor 2f, one of the most potent inhibitors synthesized to date...
Pharmacological characterization of the cloned neuropeptide Y y(6) receptorD E Mullins
Department of Central Nervous System and Cardiovascular Research, Schering Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA
Eur J Pharmacol 395:87-93. 2000..Although the function of the neuropeptide Y y(6) receptor remains to be elucidated, its pharmacology is not consistent with a role in appetite regulation...
Rational design of novel, potent piperazinone and imidazolidinone BACE1 inhibitorsJ N Cumming
Schering Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA
Bioorg Med Chem Lett 18:3236-41. 2008..The key feature of both series is a cyclic amine motif specifically crafted to achieve interactions with both the flap and with the S2' pocket...
Central melanocortin system modulates energy intake and expenditure of obese and lean Zucker ratsJ J Hwa
Schering Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, New Jersey 07033, USA
Am J Physiol Regul Integr Comp Physiol 281:R444-51. 2001..Our data suggest that a melanocortin receptor agonist can induce weight loss by increasing energy expenditure and promoting body fat utilization in addition to its inhibitory effects on food intake in both obese and lean Zucker rats...
Molecular approaches to the discovery of new treatments for obesityC D Strader
Department of CNS and Cardiovascular Research, Schering Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA
Curr Opin Chem Biol 1:204-9. 1997..Specific subtypes of the receptors for these neurotransmitters represent promising molecular targets for the discovery of new drugs for the treatment of obesity...
Calpain inhibitor I increases beta-amyloid peptide production by inhibiting the degradation of the substrate of gamma-secretase. Evidence that substrate availability limits beta-amyloid peptide productionL Zhang
Department of Central Nervous System and Cardiovascular Research, Schering Plough Research Institute, Kenilworth, New Jersey 07033, USA
J Biol Chem 274:8966-72. 1999..Rather, Abeta42 secretion may be more dependent on C100 substrate concentration than Abeta40 secretion...
Comparison of the V1b antagonist, SSR149415, and the CRF1 antagonist, CP-154,526, in rodent models of anxiety and depressionR A Hodgson
Department of Neurobiology, Schering Plough Research Institute, Kenilworth, NJ 07033, USA
Pharmacol Biochem Behav 86:431-40. 2007..This work demonstrates the different profiles of V1b and CRF1 receptor antagonists and supports both approaches in the treatment of affective disorders...
Characterization of the nociceptin receptor (ORL-1) agonist, Ro64-6198, in tests of anxiety across multiple speciesG B Varty
Department of Neurobiology, K 15 2600, Schering Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA
Psychopharmacology (Berl) 182:132-43. 2005..Previous studies have demonstrated behaviors indicative of anxiolysis in rats pretreated with the nociceptin receptor (opioid receptor like-1, ORL-1) agonist, Ro64-6198...
Discovery of an orally efficaceous 4-phenoxypyrrolidine-based BACE-1 inhibitorU Iserloh
Department of Chemical Research, Schering Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA
Bioorg Med Chem Lett 18:418-22. 2008..Due to its favorable overall profile, 11 has been extensively profiled in various in vivo settings...
Genomic organization and functional characterization of the mouse GalR1 galanin receptorS Wang
Department of CNS CV Biological Research, Schering Plough Research Institute, Kenilworth, NJ 07033, USA
FEBS Lett 411:225-30. 1997..Functional analysis of the encoded cDNA revealed active ligand binding and intracellular signaling. The expression is detected in brain, spinal cord, heart and skeletal muscle...
Measuring human beta-secretase (BACE1) activity using homogeneous time-resolved fluorescenceMatthew E Kennedy
CNS Cardiovascular Research, Schering Plough Research Institute, Kenilworth, NJ 07033, USA
Anal Biochem 319:49-55. 2003....
