4.4 Article

Drug laws and the 'derivative' problem

期刊

DRUG TESTING AND ANALYSIS
卷 6, 期 7-8, 页码 879-883

出版社

WILEY-BLACKWELL
DOI: 10.1002/dta.1523

关键词

legislation; derivatives; analogue; ecgonine; ergolines; buprenorphine

向作者/读者索取更多资源

The concept of a 'derivative' is used widely in chemistry, where its precise meaning depends on the circumstances. However, numerous examples of derivative also occur in domestic drugs legislation, some of which stem from the 1961 United Nations Single Convention on Narcotic Drugs. There is a commonly held view that only 'first-order' derivatives should be considered: substances that can be created from a parent structure in a single chemical reaction. In other words, 'derivatives of derivatives' are excluded. However, some substances related to ecgonine (e. g. 2-carbomethoxytropinone) are clearly convertible to cocaine, even though this may require more than one reaction step. It follows that 2-carbomethoxytropinone is a controlled drug, a situation that most chemists would regard as perverse. A more extreme example of the complexity of 'derivative' is shown by the conversion of thebaine to buprenorphine. Even though this requires six or more stages, the US Drug Enforcement Administration successfully argued in a 1986 case that for the purposes of the Controlled Substances Act, the number of steps required was irrelevant; buprenorphine was a derivative of thebaine. Because the term derivative is rarely defined in statutes, the legal status of some substances, such as 2-bromo-LSD, is uncertain. Although a number of definitions of derivative can be found in the chemical literature, no single definition is adequate to describe all situations where it occurs in legislation. Unless qualified, it is suggested that the term derivative should be avoided in any future legislation. Copyright (C) 2013 John Wiley & Sons, Ltd.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Biochemical Research Methods

Synthetic cannabinoid receptor agonists: Analytical profiles and development of QMPSB, QMMSB, QMPCB, 2F-QMPSB, QMiPSB, and SGT-233

Simon D. Brandt, Pierce V. Kavanagh, Folker Westphal, Wolfgang Dreiseitel, Geraldine Dowling, Matthew J. Bowden, James P. B. Williamson

Summary: Synthetic cannabinoid receptor agonists (SCRAs) are a diverse group of molecules considered new psychoactive substances (NPS) designed to explore the cannabinoid receptor system. This study extensively characterized a group of SCRAs with sulfamoyl benzoate, sulfamoyl benzamide, and N-benzoylpiperidine based structures, providing useful analytical profiles for researchers and scientists. The research performed by Stargate International set the stage for the development of these compounds, potentially leading to the emergence of new SCRAs with the quinolin-8-yl head group.

DRUG TESTING AND ANALYSIS (2021)

Article Clinical Neurology

Comparative effects of (S)-ketamine and racemic (R/S)-ketamine on psychopathology, state of consciousness and neurocognitive performance in healthy volunteers

Torsten Passie, Hans-Anton Adams, Frank Logemann, Simon D. Brandt, Birgitt Wiese, Matthias Karst

Summary: Ketamine and its enantiomers, particularly the (S)-enantiomer, have distinct psychological effects which can impact psychopathology and neurocognitive function. While (R)-ketamine appears to have fewer dissociative and psychotomimetic effects at subanesthetic doses, (S)-ketamine may induce more negative psychopathology experiences. The study suggests that the ideal composition of ketamine for treating depression should include (R)-ketamine, as it may offer protective effects against negative psychotomimetic effects compared to (S)-ketamine.

EUROPEAN NEUROPSYCHOPHARMACOLOGY (2021)

Review Biochemistry & Molecular Biology

DARK Classics in Chemical Neuroscience: Etonitazene and Related Benzimidazoles

Istvan Ujvary, Rachel Christie, Michael Evans-Brown, Ana Gallegos, Rita Jorge, Joanna de Morais, Roumen Sedefov

Summary: Etonitazene and its derivatives, developed in the late 1950s by the Swiss pharmaceutical giant CIBA, are potent analgesics with morphine-like effects. Recently, unscheduled synthetic opioids have emerged on the illicit drug market, leading to fatalities. This class of compounds has inspired research and led to the emergence of new psychoactive substances, impacting chemical neuroscience.

ACS CHEMICAL NEUROSCIENCE (2021)

Article Biochemical Research Methods

Separating the wheat from the chaff: Observations on the analysis of lysergamides LSD, MIPLA, and LAMPA

Simon D. Brandt, Pierce V. Kavanagh, Folker Westphal, Alexander Stratford, Peter Blanckaert, Geraldine Dowling, Matthias Grill, Hannes M. Schwelm, Volker Auwaerter, Stephen J. Chapman

Summary: LSD analogs like MIPLA are being sold on the street market, making it crucial to develop techniques to differentiate them from LSD. This study presents methods using gas chromatography-solid phase infrared spectroscopy and mass spectrometry to distinguish between MIPLA and LAMPA.

DRUG TESTING AND ANALYSIS (2022)

Article Biochemistry & Molecular Biology

In Vitro Metabolic Fate of the Synthetic Cannabinoid Receptor Agonists QMPSB and QMPCB (SGT-11) Including Isozyme Mapping and Esterase Activity

Matthias J. Richter, Lea Wagmann, Tanja M. Gampfer, Simon D. Brandt, Markus R. Meyer

Summary: The study identified the in vitro phase I/II metabolites of QMPSB and QMPCB and demonstrated the involvement of various monooxygenases and human carboxylesterases in their metabolism. Ester hydrolysis, hydroxylation, and formation of glucuronides and sulfates were observed. Including these metabolites in toxicological screening procedures is recommended based on the results of the in vitro experiments.

METABOLITES (2021)

Article Biochemical Research Methods

Return of the lysergamides. Part VII: Analytical and behavioural characterization of 1-valeroyl-d-lysergic acid diethylamide (1V-LSD)

Simon D. Brandt, Pierce V. Kavanagh, Folker Westphal, Benedikt Pulver, Kathleen Morton, Alexander Stratford, Geraldine Dowling, Adam L. Halberstadt

Summary: The research on the novel LSD derivative 1V-LSD suggests that it has hallucinogenic effects similar to LSD but at lower doses. Further studies on its biotransformation and receptor pharmacology are needed to fully elucidate its mechanism of action.

DRUG TESTING AND ANALYSIS (2022)

Editorial Material Biochemical Research Methods

Addressing the challenges in forensic drug chemistry II

Simon D. Brandt, Michael Collins

DRUG TESTING AND ANALYSIS (2022)

Article Biochemical Research Methods

Analytical profile, in vitro metabolism and behavioral properties of the lysergamide 1P-AL-LAD

Simon D. Brandt, Pierce Kavanagh, Folker Westphal, Benedikt Pulver, Hannes M. Schwelm, Kyla Whitelock, Alexander Stratford, Volker Auwaerter, Adam L. Halberstadt

Summary: This study characterized a novel lysergamide N,N-diethyl-1-propanoyl-6-(prop-2-en-1-yl)-9,10-didehydroergoline-8 beta-carboxamide (1P-AL-LAD) using various analytical methods. In vitro metabolism studies confirmed that 1P-AL-LAD acted as a prodrug and converted to AL-LAD as the most abundant metabolite. 1P-AL-LAD induced dose-dependent head twitch response (HTR) in mice, similar to other hallucinogenic substances.

DRUG TESTING AND ANALYSIS (2022)

Article Biochemical Research Methods

Analytical profile of the lysergamide 1cP-AL-LAD and detection of impurities

Pierce Kavanagh, Folker Westphal, Benedikt Pulver, Hannes M. Schwelm, Alexander Stratford, Volker Auwaerter, Stephen J. Chapman, Adam L. Halberstadt, Simon D. Brandt

Summary: This study describes the analysis of a novel lysergamides compound, 1cP-AL-LAD, using various chromatographic, mass spectrometric, and spectroscopic methods. The compound was found in both purchased samples and blotters sold online for recreational use. The findings provide valuable information for those interested in the chemistry of lysergamides.

DRUG TESTING AND ANALYSIS (2023)

Article Chemistry, Analytical

In Vitro Metabolic Fate of the Synthetic Cannabinoid Receptor Agonists 2F-QMPSB and SGT-233 Including Isozyme Mapping and Carboxylesterases Activity Testing

Matthias J. Richter, Lea Wagmann, Simon D. Brandt, Markus R. Meyer

Summary: The study identified in vitro metabolites of synthetic cannabinoid receptor agonists 2F-QMPSB and SGT-233, and found suitable targets for toxicological screenings. Different enzymes and human carboxylesterases were involved in their metabolism. Various CYP isoforms played important roles in the metabolism of these compounds.

JOURNAL OF ANALYTICAL TOXICOLOGY (2023)

Article Neurosciences

Use of the head-twitch response to investigate the structure-activity relationships of 4-thio-substituted 2,5-dimethoxyphenylalkylamines

Adam L. Halberstadt, Dino Luethi, Marius C. Hoener, Daniel Trachsel, Simon D. Brandt, Matthias E. Liechti

Summary: This study investigated the structure-activity relationships of 4-thio-substituted phenylalkylamines and found that these compounds have psychedelic effects, supporting their classification as psychedelics.

PSYCHOPHARMACOLOGY (2023)

Article Biochemical Research Methods

Analytical and behavioral characterization of N-ethyl-N-isopropyllysergamide (EIPLA), an isomer of N6-ethylnorlysergic acid N,N-diethylamide (ETH-LAD)

Simon D. Brandt, Pierce V. Kavanagh, Folker Westphal, Benedikt Pulver, Hannes M. Schwelm, Alexander Stratford, Volker Auwaerter, Adam L. Halberstadt

Summary: Preclinical investigations have shown that EIPLA exhibits LSD-like properties and can mimic the effects of known psychedelic drugs, making it important for forensic and clinical research.

DRUG TESTING AND ANALYSIS (2023)

Review Biochemical Research Methods

Hexahydrocannabinol and closely related semi-synthetic cannabinoids: A comprehensive review

Istvan Ujvary

Summary: Since the early 2000s, the global illicit cannabinoid market has been in turmoil with the emergence of unregulated synthetic cannabinoids and more recently, semi-synthetic cannabinoids made from hemp extracts. The production of these semi-synthetic cannabinoids, such as hexahydrocannabinol (HHC), was triggered by changes in US legislation regarding hemp cultivation. Current large-scale manufacture of HHC is based on hemp-derived CBD extract and involves cyclization and catalytic hydrogenation processes. While preclinical studies have shown THC-like properties in (9R)-HHC, the human pharmacology and metabolism of HHC are still unknown, and there is a lack of (immuno)analytical methods for rapid detection of HHC or its metabolites in urine. This review provides an overview of the legal background, chemistry, analysis, and pharmacology of HHC and related analogs, including HHC acetate (HHC-O).

DRUG TESTING AND ANALYSIS (2023)

Article Biochemical Research Methods

Acute psychotropic, autonomic, and endocrine effects of 5,6-methylenedioxy-2-aminoindane (MDAI) compared with 3,4-methylenedioxymethamphetamine (MDMA) in human volunteers: A self-administration study

Verena Angerer, Yasmin Schmid, Florian Franz, Heike Gnann, Jan Manuel Speer, Anke Gnann, Stephan Helmecke, Armin Buchwald, Simon D. Brandt, Torsten Passie, Matthias E. Liechti, Volker Auwaerter

Summary: Administration of the new psychoactive substance 5,6-methylenedioxy-2-aminoindane (MDAI) to six volunteers revealed that acute subjective effects were qualitatively comparable with 3,4-methylenedioxymethamphetamine (MDMA) based on psychometric measures. Physiological and endocrine measures were also included. In serum and urine, MDAI could be detected for at least 4 and 6 days.

DRUG TESTING AND ANALYSIS (2023)

Article Chemistry, Medicinal

Investigation of the Structure-Activity Relationships of Psilocybin Analogues

Adam K. Klein, Muhammad Chatha, Lauren J. Laskowski, Emilie Anderson, Simon D. Brandt, Stephen J. Chapman, John D. McCorvy, Adam L. Halberstadt

Summary: This study investigated the pharmacological properties of tryptamine derivatives containing N,N-dialkyl substituents and a 4-hydroxy or 4-acetoxy group, revealing their similar potencies at 5-HT2A and 5-HT2B receptors. The compounds acted as full or partial agonists at 5-HT2 subtypes and induced LSD-like head twitches in mice. O-acetylation reduced the in vitro potency of the compounds but had little effect on their in vivo head twitch response potency, suggesting a prodrug mechanism.

ACS PHARMACOLOGY & TRANSLATIONAL SCIENCE (2021)

暂无数据