Recent developments in the medicinal chemistry of cannabimimetic indoles, pyrroles and indenes.
about
Cannabinergic aminoalkylindoles, including AM678=JWH018 found in 'Spice', examined using drug (Δ(9)-tetrahydrocannabinol) discrimination for ratsBeyond THC: The New Generation of Cannabinoid Designer DrugsWithdrawal phenomena and dependence syndrome after the consumption of "spice gold"Spice drugs are more than harmless herbal blends: a review of the pharmacology and toxicology of synthetic cannabinoidsTargeting cannabinoid agonists for inflammatory and neuropathic painDistinct pharmacology and metabolism of K2 synthetic cannabinoids compared to Δ(9)-THC: mechanism underlying greater toxicity?Fluorinated cannabinoid CB2 receptor ligands: synthesis and in vitro binding characteristics of 2-oxoquinoline derivativesEvaluation of a homogenous enzyme immunoassay for the detection of synthetic cannabinoids in urineCross-substitution of Δ9-tetrahydrocannabinol and JWH-018 in drug discrimination in rats.8-Chloro- and 5,8-Dichloro1-naphthoic Acids.1-Pentyl-3-phenylacetylindoles and JWH-018 share in vivo cannabinoid profiles in miceMoving around the molecule: relationship between chemical structure and in vivo activity of synthetic cannabinoids.AB-CHMINACA, AB-PINACA, and FUBIMINA: Affinity and Potency of Novel Synthetic Cannabinoids in Producing Δ9-Tetrahydrocannabinol-Like Effects in MiceBaths salts, spice, and related designer drugs: the science behind the headlines.Alkylindole-sensitive receptors modulate microglial cell migration and proliferation.Synthesis and pharmacology of 1-alkyl-3-(1-naphthoyl)indoles: steric and electronic effects of 4- and 8-halogenated naphthoyl substituentsAssessment of the Abuse Liability of Synthetic Cannabinoid Agonists JWH-030, JWH-175, and JWH-176.Cytochrome P450-mediated oxidative metabolism of abused synthetic cannabinoids found in K2/Spice: identification of novel cannabinoid receptor ligands.Spicing things up: synthetic cannabinoids.Synthetic cannabinoids and potential reproductive consequences.Cannabinoids in disguise: Δ9-tetrahydrocannabinol-like effects of tetramethylcyclopropyl ketone indoles.Assessing the experience of using synthetic cannabinoids by means of interpretative phenomenological analysis.Some new psychoactive substances: precursor chemicals and synthesis-driven end-products.Acute kidney injury associated with smoking synthetic cannabinoid.Increases in synthetic cannabinoids-related harms: Results from a longitudinal web-based content analysis.Recent Advances in the Synthesis of Indanes and Indenes.Combination Chemistry: Structure-Activity Relationships of Novel Psychoactive Cannabinoids.Pharmacological and Toxicological Effects of Synthetic Cannabinoids and Their Metabolites.Synthetic Cathinone and Cannabinoid Designer Drugs Pose a Major Risk for Public Health.Synthetic approaches to multifunctional indenes.The Influence of Synthetic Cannabinoid UR-144 on Human Psychomotor Performance--A Case Report Demonstrating Road Traffic Risks.Synthetic cannabinoid induced acute respiratory depression: Case series and literature review.Evaluation of first generation synthetic cannabinoids on binding at non-cannabinoid receptors and in a battery of in vivo assays in mice.Stabilized pyrrolyl iodonium salts and metal-free oxidative cross-coupling.Ferric chloride-catalyzed C-N bond cleavage for the cyclization of arylallenes leading to polysubstituted indenes.Indium triflate catalyzed microwave-assisted alkenylation of methoxyphenols: synthesis of indenes and chromenesDiscovery of High-Affinity Cannabinoid Receptors Ligands through a 3D-QSAR Ushered by Scaffold-Hopping AnalysisIdentification and structural characterization of the synthetic cannabinoid 3-(1-adamantoyl)-1-pentylindole as an additive in ‘herbal incense’Identification of the major urinary metabolites in man of seven synthetic cannabinoids of the aminoalkylindole type present as adulterants in ‘herbal mixtures’ using LC-MS/MS techniquesMechanism of the N-protecting group dependent annulations of 3-aryloxy alkynyl indoles under gold catalysis: a computational study
P2860
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P2860
Recent developments in the medicinal chemistry of cannabimimetic indoles, pyrroles and indenes.
description
2005 nî lūn-bûn
@nan
2005 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Recent developments in the med ...... indoles, pyrroles and indenes.
@ast
Recent developments in the med ...... indoles, pyrroles and indenes.
@en
type
label
Recent developments in the med ...... indoles, pyrroles and indenes.
@ast
Recent developments in the med ...... indoles, pyrroles and indenes.
@en
prefLabel
Recent developments in the med ...... indoles, pyrroles and indenes.
@ast
Recent developments in the med ...... indoles, pyrroles and indenes.
@en
P356
P1476
Recent developments in the med ...... indoles, pyrroles and indenes.
@en
P2093
Huffman JW
Padgett LW
P304
P356
10.2174/0929867054020864
P577
2005-01-01T00:00:00Z