5-HT3 receptors

AJ Thompson, SC R Lummis - Current pharmaceutical design, 2006 - ingentaconnect.com
The 5-HT3 receptor is a member of the Cys-loop family of ligand-gated ion channels. These
receptors are located in both the peripheral and central nervous systems, where functional …

5-HT3 receptor antagonists in neurologic and neuropsychiatric disorders: the iceberg still lies beneath the surface

G Fakhfouri, R Rahimian, J Dyhrfjeld-Johnsen… - Pharmacological …, 2019 - Elsevier
HT 3 receptor antagonists, first introduced to the market in the mid-1980s, are proven
efficient agents to counteract chemotherapy-induced emesis. Nonetheless, recent …

Recent advances with 5‐HT3 modulators for neuropsychiatric and gastrointestinal disorders

R Juza, P Vlcek, E Mezeiova, K Musilek… - Medicinal research …, 2020 - Wiley Online Library
Abstract Serotonin (5‐hydroxytryptophan [5‐HT]) is a biologically active amine expressed in
platelets, in gastrointestinal (GI) cells and, to a lesser extent, in the central nervous system …

The role of 5-HT3 receptors in drug abuse and as a target for pharmacotherapy

EA Engleman, ZA Rodd, RL Bell… - CNS & Neurological …, 2008 - ingentaconnect.com
Alcohol and drug abuse continue to be a major public health problem in the United States
and other industrialized nations. Extensive preclinical research indicates the mesolimbic …

Synthesis of N-Guanidinium-Chitosan/Silica Hybrid Composites: Efficient Adsorbents for Anionic Pollutants

A Salama, P Hesemann - Journal of Polymers and the Environment, 2018 - Springer
A new chitosan derivative, N-guanidinium chitosan acetate, has been synthesized by direct
guanylation of chitosan by cyanamide in presence of scandium (III) triflate under mild acidic …

Novel Potent and Selective Central 5-HT3 Receptor Ligands Provided with Different Intrinsic Efficacy. 1. Mapping the Central 5-HT3 Receptor Binding Site by …

A Cappelli, M Anzini, S Vomero… - Journal of medicinal …, 1998 - ACS Publications
Synthesis and pharmacological evaluation of a series of condensed quinoline and pyridine
derivatives bearing a N-methylpiperazine moiety attached to the 2-position of the quinoline …

2-Amino-6-chloro-3, 4-dihydroquinazoline: A novel 5-HT3 receptor antagonist with antidepressant character

M Dukat, K Alix, J Worsham, S Khatri… - Bioorganic & medicinal …, 2013 - Elsevier
Amino-6-chloro-3, 4-dihydroquinazoline HCl (A6CDQ, 4) binds at 5-HT 3 serotonin
receptors and displays antidepressant-like action in the mouse tail suspension test (TST) …

Direct guanylation of amino groups by cyanamide in water: catalytic generation and activation of unsubstituted carbodiimide by scandium (III) triflate

K Tsubokura, T Iwata, M Taichi, A Kurbangalieva… - Synlett, 2014 - thieme-connect.com
Guanylation proceeded efficiently upon treatment of the various amines with cyanamide in
the presence of catalytic amounts of scandium (III) triflate under mild conditions. The method …

Combined effects of neurotrophin secreting transplants, exercise, and serotonergic drug challenge improve function in spinal rats

JM Nothias, T Mitsui, JS Shumsky… - … and Neural Repair, 2005 - journals.sagepub.com
Objectives. To determine the effects of neurotrophin-secreting transplants combined with
exercise and serotonergic drug challenges on recovery of hindlimb function in rats with …

The serotonergic 5-HT2C agonist m-chlorophenylpiperazine increases weight-supported locomotion without development of tolerance in rats with spinal transections

D Kim, M Murray, KJ Simansky - Experimental neurology, 2001 - Elsevier
The direct serotonergic agonist, m-chlorophenylpiperazine (m-CPP), displays high efficacy
at 5-HT2C receptors. Systemic administration of m-CPP increased dramatically the …