Search Results - "Huailing Zhong"
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Escitalopram, an antidepressant with an allosteric effect at the serotonin transporter—a review of current understanding of its mechanism of action
Published in Psychopharmacologia (2012)“…Rationale Escitalopram is a widely used antidepressant for the treatment of patients with major depression. It is the pure S-enantiomer of racemic citalopram…”
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Discovery of 1-[2-(2,4-Dimethylphenylsulfanyl)phenyl]piperazine (Lu AA21004): A Novel Multimodal Compound for the Treatment of Major Depressive Disorder
Published in Journal of medicinal chemistry (12-05-2011)“…The synthesis and structure−activity relationship of a novel series of compounds with combined effects on 5-HT3A and 5-HT1A receptors and on the serotonin…”
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3
Small-molecule antagonists of melanopsin-mediated phototransduction
Published in Nature chemical biology (01-10-2013)“…Opsinamides are nonretinoid inhibitors that compete with 9- cis -retinal for binding to melanopsin Opn4 without affecting rod- and cone-mediated visual…”
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Regulator of G protein signaling proteins: novel multifunctional drug targets
Published in The Journal of pharmacology and experimental therapeutics (01-06-2001)“…G protein-coupled receptors (GPCRs) play a major role in signal transduction and are targets of many therapeutic drugs. The regulator of G protein signaling…”
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Anxiolytic- and Antidepressant-like Profiles of the Galanin-3 Receptor ($Gal_3$) Antagonists SNAP 37889 and SNAP 398299
Published in Proceedings of the National Academy of Sciences - PNAS (29-11-2005)“…The neuropeptide galanin mediates its effects through the receptor subtypes$Gal_1$,$Gal_2$, and$Gal_3$and has been implicated in anxiety-and depression-related…”
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An allosteric binding site at the human serotonin transporter mediates the inhibition of escitalopram by R-citalopram: Kinetic binding studies with the ALI/VFL–SI/TT mutant
Published in Neuroscience letters (25-09-2009)“…The human serotonin transporter (hSERT) has primary and allosteric binding sites for escitalopram and R-citalopram. Previous studies have established that the…”
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Cocaine induction of dopamine transporter trafficking to the plasma membrane
Published in Molecular pharmacology (01-02-2002)“…Several previous human postmortem experiments have detected an increase in striatal [(3)H]WIN 35428 binding to the dopamine transporter (DAT) in chronic…”
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The novel neuropeptide Y Y5 receptor antagonist Lu AA33810 [N-[[trans-4-[(4,5-dihydro[1]benzothiepino[5,4-d]thiazol-2-yl)amino]cyclohexyl]methyl]-methanesulfonamide] exerts anxiolytic- and antidepressant-like effects in rat models of stress sensitivity
Published in The Journal of pharmacology and experimental therapeutics (01-03-2009)“…Neuropeptide Y (NPY) regulates physiological processes via receptor subtypes (Y(1), Y(2), Y(4), Y(5), and y(6)). The Y(5) receptor is well known for its role…”
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A Spatial Focusing Model for G Protein Signals
Published in The Journal of biological chemistry (28-02-2003)“…Regulators of G protein signaling (RGS) are GTPase-accelerating proteins (GAPs), which can inhibit heterotrimeric G protein pathways. In this study, we provide…”
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Label-free pharmacological profiling based on dynamic mass redistribution for characterization and authentication of hazardous natural products
Published in Journal of hazardous materials (05-07-2017)“…[Display omitted] •Dynamic mass redistribution (DMR) profiling was proposed to characterize toxic herbs.•Qualitative DMR profiling has obvious advantages over…”
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A label-free screening approach targeted protease-activated receptor 1 based on dynamic mass redistribution in living cells
Published in RSC advances (2017)“…Protease-activated receptor 1 (PAR-1) antagonists strongly inhibit thrombin-induced platelet aggregation and are proved to be effective as anti-thrombotic…”
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Consideration of allosterism and interacting proteins in the physiological functions of the serotonin transporter
Published in Biochemical pharmacology (15-02-2012)“…The serotonin transporter (SERT) functions to transport serotonin (5-HT) from the extracellular space into neurons to maintain homeostatic control of 5-HT. It…”
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A label-free screening approach targeted protease-activated receptor 1 based on dynamic mass redistribution in living cellsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ra07927c
Published 05-09-2017“…Protease-activated receptor 1 (PAR-1) antagonists strongly inhibit thrombin-induced platelet aggregation and are proved to be effective as anti-thrombotic…”
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Endogenous RGS Proteins and Gα Subtypes Differentially Control Muscarinic and Adenosine-Mediated Chronotropic Effects
Published in Circulation research (17-03-2006)“…Cardiac automaticity is controlled by G protein–coupled receptors, such as adrenergic, muscarinic, and adenosine receptors. The strength and duration of G…”
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RGS-insensitive G-protein mutations to study the role of endogenous RGS proteins
Published in Methods in enzymology (2004)“…Regulator of G-protein signaling (RGS) proteins are very active GTPase-accelerating proteins (GAPs) in vitro and are expected to reduce signaling by G-protein…”
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Endogenous RGS proteins and ga subtypes differentially control muscarinic and adenosine-mediated chronotropic effects
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Endogenous RGS protein action modulates mu-opioid signaling through Galphao. Effects on adenylyl cyclase, extracellular signal-regulated kinases, and intracellular calcium pathways
Published in The Journal of biological chemistry (14-03-2003)“…RGS (regulators of G protein signaling) proteins are GTPase-activating proteins for the Galpha subunits of heterotrimeric G proteins and act to regulate…”
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Endogenous RGS Protein Action Modulates μ-Opioid Signaling through Gαo
Published in The Journal of biological chemistry (14-03-2003)“…RGS ( r egulators of G protein s ignaling) proteins are GTPase-activating proteins for the Gα subunits of heterotrimeric G proteins and act to regulate…”
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Endogenous RGS Protein Action Modulates μ-Opioid Signaling through Gαo
Published in The Journal of biological chemistry (01-03-2003)Get full text
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Structure-based design, synthesis, and activity of peptide inhibitors of RGS4 GAP activity
Published in Methods in enzymology (2004)“…One of the principal roles of the multifunctional regulator of G-protein signaling (RGS) proteins is to terminate G-protein-coupled receptor (GPCR) signaling…”
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