Evidence map›Paper›PMID 31756337›Full record

ArticleNeuropharmacology2020

Pharmacological and biotransformation studies of 1-acyl-substituted derivatives of d-lysergic acid diethylamide (LSD).

Adam L Halberstadt, Muhammad Chatha, Adam K Klein, John D McCorvy, Markus R Meyer, Lea Wagmann, Alexander Stratford, Simon D Brandt

Open access · greenAbstract read
In one paragraph

Article in Neuropharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.2field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  12. Targeting Serotonin 5-HTCNS drugs · 2020
    Review
  13. Article
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 4 countries.

Adam L HalberstadtDepartment of Psychiatry, University of California San Diego, La Jolla, CA, 92093-0804, USA; Research Service, VA San Diego Healthcare System, 3350 La Jolla Village Dr, San Diego, CA, 92161, USA. Electronic address: ahalberstadt@ucsd.edu.
Muhammad ChathaDepartment of Psychiatry, University of California San Diego, La Jolla, CA, 92093-0804, USA.
Adam K KleinDepartment of Psychiatry, University of California San Diego, La Jolla, CA, 92093-0804, USA.
John D McCorvyDepartment of Cell Biology, Neurobiology & Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA.
Markus R MeyerDepartment of Experimental and Clinical Toxicology, Institute of Experimental and Clinical Pharmacology and Toxicology, Center for Molecular Signaling (PZMS), Saarland University, 66421, Homburg, Germany.
Lea WagmannDepartment of Experimental and Clinical Toxicology, Institute of Experimental and Clinical Pharmacology and Toxicology, Center for Molecular Signaling (PZMS), Saarland University, 66421, Homburg, Germany.
Alexander StratfordSynex Synthetics BV, Karveelweg 20, 6222NH, Maastricht, the Netherlands.
Simon D BrandtSchool of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Byrom Street, Liverpool, L3 3AF, UK.
University of California, San Diego · USSaarland University · DELiverpool John Moores University · GBMedical College of Wisconsin · USSynapse (Netherlands) · NL

Funding

The Next Generation of Hallucinogens: A New Class of Synthetic Psychoactive DrugsR01DA041336 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HALBERSTADT, ADAM L. · 2017 to 2020
$1.4M
NIDA NIH HHS R01 DA041336NIMH NIH HHS HHSN271200800025C
6 · The paper itself

Abstract

The ergoline d-lysergic acid diethylamide (LSD) is one of the most potent psychedelic drugs. 1-Acetyl-LSD (ALD-52), a derivative of LSD containing an acetyl group on the indole nitrogen, also produces psychedelic effects in humans and has about the same potency as LSD. Recently, several other 1-acyl-substitued LSD derivatives, including 1-propanoyl-LSD (1P-LSD) and 1-butanoyl-LSD (1B-LSD), have appeared as designer drugs. Although these compounds are assumed to act as prodrugs for LSD, studies have not specifically tested this prediction. The present investigation was conducted to address the gap of information about the pharmacological effects and mechanism-of-action of 1-acyl-substituted LSD derivatives. Competitive binding studies and calcium mobilization assays were performed to assess the interaction of ALD-52, 1P-LSD, and 1B-LSD with serotonin 5-HT

Indexed as

AnimalsBehavior, AnimalBinding, CompetitiveBiotransformationCalcium SignalingDrug Evaluation, PreclinicalHallucinogensLysergic Acid DiethylamideMaleMiceMice, Inbred C57BLProdrugsRatsRats, Sprague-DawleyReceptors, Serotonin, 5-HT2Serotonin 5-HT2 Receptor AgonistsHallucinogensLysergic Acid DiethylamideProdrugsReceptors, Serotonin, 5-HT2Serotonin 5-HT2 Receptor AgonistsSerotonin 5-HT2 Receptor Antagonists5-HT(2A) receptorLSDLysergamidesNew psychoactive substancesPsychedelics

Identifiers

PMID31756337
PMCPMC9191647
OpenAlexW2991486694

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.