Search Results - "Glennon, R A"
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Abuse-related and abuse-limiting effects of methcathinone and the synthetic “bath salts” cathinone analogs methylenedioxypyrovalerone (MDPV), methylone and mephedrone on intracranial self-stimulation in rats
Published in Psychopharmacology (01-01-2014)“…Rationale Abuse of synthetic cathinones, popularized as “bath salts,” has increased dramatically in the USA since their debut in 2010. Preclinical behavioral…”
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Structural Modification of the Designer Stimulant α‑Pyrrolidinovalerophenone (α-PVP) Influences Potency at Dopamine Transporters
Published in ACS chemical neuroscience (21-10-2015)“…α-Pyrrolidinovalerophenone (α-PVP, 7) is an illegal synthetic stimulant that is being sold on the clandestine market as “flakka” and “gravel”. The potent…”
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Stereoselective Actions of Methylenedioxypyrovalerone (MDPV) To Inhibit Dopamine and Norepinephrine Transporters and Facilitate Intracranial Self-Stimulation in Rats
Published in ACS chemical neuroscience (20-05-2015)“…The designer stimulant methylenedioxypyrovalerone (MDPV) is a potent reuptake inhibitor at transporters for dopamine (DAT) and norepinephrine (NET) that…”
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Pharmacophore identification for sigma-1 (sigma1) receptor binding: application of the "deconstruction-reconstruction-elaboration" approach
Published in Mini reviews in medicinal chemistry (01-10-2005)“…At least two different types of sigma (sigma1 and sigma2) receptors have been identified. A structural feature common to high-affinity (Ki <10 nM) sigma1…”
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Antinociceptive responses to nicotinic acetylcholine receptor ligands after systemic and intrathecal administration in mice
Published in The Journal of pharmacology and experimental therapeutics (01-03-1998)“…The objective of this study was to determine which nicotinic receptor subtypes are involved in antinociception and their site of action. For that, the…”
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Quantitative structure–activity relationship analysis of the pharmacology of para‐substituted methcathinone analogues
Published in British journal of pharmacology (01-05-2015)“…Background and Purpose Methcathinone (MCAT) is a potent monoamine releaser and parent compound to emerging drugs of abuse including mephedrone (4‐CH3 MCAT),…”
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Binding of β-carbolines at 5-HT2 serotonin receptors
Published in Bioorganic & medicinal chemistry letters (15-12-2003)Get full text
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Steric parameters, molecular modeling and hydropathic interaction analysis of the pharmacology of para‐substituted methcathinone analogues
Published in British journal of pharmacology (01-05-2015)“…Background and Purpose There is growing concern over the abuse of certain psychostimulant methcathinone (MCAT) analogues. This study extends an initial…”
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Homoazanicotine: A Structure-Affinity Study for Nicotinic Acetylcholine (nACh) Receptor Binding
Published in Journal of medicinal chemistry (10-10-2002)“…We have recently identified 3-[(1-methyl)-4,5-dihydro-1H-imidazol-2-yl)methyl]pyridine (homoazanicotine, 8) as a novel nicotinic acetylcholinergic (nACh)…”
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Radioligand binding evidence implicates the brain 5-HT2 receptor as a site of action for LSD and phenylisopropylamine hallucinogens
Published in Psychopharmacologia (01-02-1988)“…Alterations in brain serotonergic function have been implicated in the mechanism of action of LSD, mescaline, and other similarly acting hallucinogenic drugs…”
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Is a nitrogen atom an important pharmacophoric element in sigma ligand binding ?
Published in Bioorganic & medicinal chemistry (01-08-2000)“…A lingering question in sigma receptor ligand development is whether a nitrogen atom serves as an important pharmacophoric element in binding affinity. To…”
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Central serotonin receptors as targets for drug research
Published in Journal of medicinal chemistry (01-01-1987)Get full text
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Cathinone: An Investigation of Several N-Alkyl and Methylenedioxy-Substituted Analogs
Published in Pharmacology, biochemistry and behavior (01-12-1997)“…DAL CASON, T. A., R. YOUNG AND R. A. GLENNON. Cathinone: An investigation of several N -alkyl and methylenedioxy-substituted analogs. PHARMACOL BIOCHEM BEHAV…”
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Lobeline: Structure−Affinity Investigation of Nicotinic Acetylcholinergic Receptor Binding
Published in Journal of medicinal chemistry (09-09-1999)“…(−)Lobeline (1) and (−)nicotine (2) bind at neuronal nicotinic cholinergic (nACh) receptors with high affinity (K i = 4 and 2 nM, respectively). Previous…”
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Autoradiographic characterization of (+-)-1-(2,5-dimethoxy-4-[125I] iodophenyl)-2-aminopropane ([125I]DOI) binding to 5-HT2 and 5-HT1c receptors in rat brain
Published in The Journal of pharmacology and experimental therapeutics (01-11-1990)“…The 5-HT2 (serotonin) receptor has traditionally been labeled with antagonist radioligands such as [3H]ketanserin and [3H]spiperone, which label both agonist…”
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Behavioral characterization of 2- O-desmethyl and 5- O-desmethyl metabolites of the phenylethylamine hallucinogen DOM
Published in Pharmacology, biochemistry and behavior (01-07-2003)“…The present investigation was undertaken to test the hypothesis that known metabolites of the phenylethylamine hallucinogen…”
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Binding of nicotine and homoazanicotine analogues at neuronal nicotinic acetylcholinergic (nACh) receptors
Published in Bioorganic & medicinal chemistry letters (24-02-2003)“…A total of 20 substituted analogues of nicotine ( 1a) and homoazanicotine ( 3a) were examined in order to determine whether or not they might bind in a similar…”
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Investigation of hallucinogenic and related β-carbolines
Published in Drug and alcohol dependence (01-04-1998)“…Certain β-carbolines are known to be hallucinogenic in humans, and several produce stimulus effects in animals similar to those of the classical hallucinogen…”
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Differential ergoline and ergopeptine binding to 5-hydroxytryptamine2A receptors: ergolines require an aromatic residue at position 340 for high affinity binding
Published in Molecular pharmacology (01-03-1995)“…In this paper we show that a highly conserved aromatic residue, phenylalanine at the 340-position, is essential for ergoline binding to 5-hydroxytryptamine2A…”
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