Author:
Arias Hugo R.,Tae Han-Shen,Micheli Laura,Yousuf Arsalan,Ghelardini Carla,Adams David J.,Di Cesare Mannelli Lorenzo
Funder
MIUR
University of Florence
Australian Research Council
Oklahoma State University
Subject
Cellular and Molecular Neuroscience,Pharmacology
Cited by
14 articles.
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1. The novel non-hallucinogenic compound DM506 (3-methyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole) induces sedative- and anxiolytic-like activity in mice by a mechanism involving 5-HT2A receptor activation;European Journal of Pharmacology;2024-03
2. Exploring Cholinergic Compounds for Peripheral Neuropathic Pain Management: A Comprehensive Scoping Review of Rodent Model Studies;Pharmaceuticals;2023-09-27
3. Coronaridine congeners induce sedative and anxiolytic-like activity in naïve and stressed/anxious mice by allosteric mechanisms involving increased GABAA receptor affinity for GABA;European Journal of Pharmacology;2023-08
4. DM506 (3-Methyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole fumarate), a Novel Derivative of Ibogamine, Inhibits α7 and α9α10 Nicotinic Acetylcholine Receptors by Different Allosteric Mechanisms;ACS Chemical Neuroscience;2023-06-30
5. The Antinociceptive Activity of (E)-3-(thiophen-2-yl)-N-(p-tolyl)acrylamide in Mice Is Reduced by (E)-3-(furan-2-yl)-N-methyl-N-(p-tolyl)acrylamide Through Opposing Modulatory Mechanisms at the α7 Nicotinic Acetylcholine Receptor;Anesthesia & Analgesia;2023-04-14