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5-MeO-DMT: all studies

Page 26 of 110: studies 251 to 260 of 1,096, newest first. Back to the 5-MeO-DMT overview

Research

Characterisation of a proposed internet synthesis of N,N-dimethyltryptamine using liquid chromatography/electrospray ionisation tandem mass spectrometry.

Journal of Chromatography A August 14, 2009 Cláudia P.B. Martins, Sally Freeman, John F. Alder et al. 11 citations

The psychoactive properties of N,N-dimethyltryptamine (DMT) are known to induce altered states of consciousness in humans. These properties attract great interest from clinical, neuroscientific, clandestine and forensic communities. The Breath of Hope Synthesis was reported on an internet website as a convenient two-step methodology for the preparation of DMT. The analytical characterisation of...

Comparison of the developmental effects of 5-methoxy-N,N-diisopropyltryptamine (Foxy) to (+/-)-3,4-methylenedioxymethamphetamine (ecstasy) in rats.

Psychopharmacology June 1, 2009 Matthew R. Skelton, Tori L. Schaefer, Nicole R Herring et al. 31 citations

We have previously shown that (+/-)-3,4-methylenedioxymethamphetamine (MDMA) treatment from postnatal days (P)11 to P20 leads to learning and memory deficits when the animals are tested as adults. Recently, the club drug 5-methoxy-N,N-diisopropyltryptamine (5-MeO-DIPT) has gained popularity. Due to the similarities between MDMA and 5-MeO-DIPT and the substitution of 5-MeO-DIPT for MDMA, the...

Development of a LC–MS/MS Method to Analyze 5-Methoxy-N,N-Dimethyltryptamine and Bufotenine: Application to Pharmacokinetic Study

Bioanalysis March 27, 2009 Hong-Wu Shen, Xi-Ling Jiang, Ai-Ming Yu 26 citations

INTRODUCTION: 5-Methoxy-N,N-dimethyltryptamine (5-MeO-DMT) is a psychoactive indolealkylamine substance that has been used for recreational purpose and may lead to fatal toxicity. While 5-MeO-DMT is mainly inactivated via deamination, it is O-demethylated to an active metabolite, bufotenine. Quantitation of 5-MeO-DMT and bufotenine is essential to understand the exposure to and the effects of...

DOI: 10.4155/bio.09.7 (opens in new tab) Chromatography Metabolite Protein precipitation Pharmacokinetics +1

When the Endogenous Hallucinogenic Trace AmineN,N-Dimethyltryptamine Meets the Sigma-1 Receptor

Science Signaling March 10, 2009 Tsung‐ping Su, Teruo Hayashi, D. Bruce Vaupel 110 citations

N,N-dimethyltryptamine (DMT) is a hallucinogen found endogenously in human brain that is commonly recognized to target the 5-hydroxytryptamine 2A receptor or the trace amine-associated receptor to exert its psychedelic effect. DMT has been recently shown to bind sigma-1 receptors, which are ligand-regulated molecular chaperones whose function includes inhibiting various voltage-sensitive ion...

DOI: 10.1126/scisignal.261pe12 (opens in new tab) Hallucinogen Endogeny Pharmacology Receptor +1

Modification of the effects of 5-methoxy-N,N-dimethyltryptamine on exploratory behavior in rats by monoamine oxidase inhibitors.

Psychopharmacology November 1, 2008 Adam L. Halberstadt, Mahalah R Buell, Virginia L Masten et al. 46 citations

The hallucinogenic tea known as ayahuasca is made from a combination of psychoactive plants that contribute the active components N,N-dimethyltryptamine (DMT) and 5-methoxy-DMT (5-MeO-DMT), as well as the monoamine oxidase (MAO) inhibitors (MAOIs) harmine and harmaline for oral activity. The present study examined the effects of 5-MeO-DMT in combination with MAOIs in rats using the behavioral...

Dried Toad Venom ‘Aphrodisiacs’ Lead to Fatal Poisonings

Emergency Medicine News August 1, 2008 Leon Gussow

It wasn't the first time a New York City hospital saw a fatal case of aphrodisiac toxicity. In May, the New York Times reported that a 35-year-old man died after ingesting an illegal aphrodisiac sold under the street name “Stone” (or “Piedra,” Spanish for “stone”). He presented to a local emergency department 12 hours after ingestion complaining of abdominal pain. Evaluation revealed...

Halogenated solvent interactions with N,N-dimethyltryptamine: formation of quaternary ammonium salts and their artificially induced rearrangements during analysis.

Forensic Science International July 4, 2008 Simon D. Brandt, Cláudia P.B. Martins, Sally Freeman et al. 10 citations

The psychoactive properties of N,N-dimethyltryptamine (DMT) 1a are known to induce altered states of consciousness in humans. This particular attribute attracts great interest from a variety of scientific and also clandestine communities. Our recent research has confirmed that DMT reacts with dichloromethane (DCM), either as a result of work-up or storage to give a quaternary N-chloromethyl...

Oxidation of 5-methoxy-N,N-diisopropyltryptamine in rat liver microsomes and recombinant cytochrome P450 enzymes.

Biochemical Pharmacology February 1, 2008 Shizuo Narimatsu, Rei Yonemoto, Kazufumi Masuda et al.

The oxidative metabolism of 5-methoxy-N,N-diisopropyltryptamine (5-MeO-DIPT), a tryptamine-type designer drug, was studied using rat liver microsomal fractions and recombinant cytochrome P450 (CYP) enzymes. 5-MeO-DIPT was biotransformed mainly into a side-chain N-deisopropylated metabolite and partially into an aromatic ring O-demethylated metabolite in liver microsomal fractions from untreated...

Neuropsychotoxicity of abused drugs: molecular and neural mechanisms of neuropsychotoxicity induced by methamphetamine, 3,4-methylenedioxymethamphetamine (ecstasy), and 5-methoxy-N,N-diisopropyltryptamine (foxy).

Journal of Pharmacological Sciences 2008 Takayuki Nakagawa, Shuji Kaneko 44 citations

Psychostimulants including amphetamines and cocaine, opioids including morphine, and some recreational drugs share the ability to cause drug dependence and addiction. Although these drugs of abuse primarily act on distinct molecular targets, such as monoamine transporters or receptors, they finally converge to common neural pathways. Several lines of evidence suggest that their chronic...

N,N-Dimethyltryptamine and dichloromethane: Rearrangement of quaternary ammonium salt product during GC–EI and CI-MS–MS analysis

Journal of Pharmaceutical and Biomedical Analysis December 28, 2007 Simon D. Brandt, Cláudia P.B. Martins, Sally Freeman et al. 10 citations

N,N-Dimethyltryptamine (DMT) 1 is a simple tryptamine derivative with powerful psychoactive properties. It is abundant in nature and easily accessible through a variety of synthetic routes. Most work-up procedures require the use of organic solvents and halogenated representatives are often employed. DMT was found to be reactive towards dichloromethane, either during work-up or long term...

DOI: 10.1016/j.jpba.2007.12.024 (opens in new tab) Dichloromethane Tryptamine Gas chromatography–mass spectrometry Indole test +3