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Downloaded Popular in Europe, and the “Rave” (An All Night Dance Party) from the Web [4]
The Open Forensic Science Journal, 2011, 4, 20-24 20 Open Access A Historical Review of MDMA Steven B. Karch* Berkeley, California 94705, USA Abstract: In less than 50 years the number of MDMA (3,4-Methylenedioxymethamphetamine or Ecstasy) users in the United States has gone from zero to nearly three million. For all of its popularity, very little is known about MDMA’s probable mechanism of action, or the mechanisms by which it causes death and disability. Even less is known about this drug’s checkered past, including dangerous plans by various government agencies to “weaponize” MDMA, and misleading research sponsored and propagated by the U.S. government. Recently, evidence has begun to emerge that MDMA may cause valvular heart disease and possibly myocardial disease as well. These issues have not yet appeared on the media radar. For that reason, an historical review of this fascinating drug was undertaken here. Keywords: Ecstacy, Shulgin, history, MK-Ultra, psychoactive, serotonin, empathogen, myocardial fibrosis, neurotoxicity. MDA, Club drugs, Raves. INTRODUCTION as a precursor compound, and never even evaluated MDMA’s basic physiologic properties until years after the Estimates of the United Nations suggest that in North patent for MDMA was actually awarded. America there are approximately 2.6 million MDMA (3,4- Methylenedioxymethamphetamine or Ecstasy) users, mostly Fifteen years passed before Merck made any effort to in the United States. The annual prevalence of MDMA use systematically evaluate MDMA’s pharmacologic effects in within the general U.S. population is approximately 0.9%, animals. The first experiments were carried out in 1927. -
Update of the Generic Definition for Tryptamines
ACMD Advisory Council on the Misuse of Drugs Chair: Professor Les Iversen Secretary: Zahi Sulaiman 2nd Floor (NW), Seacole Building 2 Marsham Street London SW1P 4DF Tel: 020 7035 1121 [email protected] Norman Baker MP, Minister for Crime Prevention Home Office 2 Marsham Street London SW1P 4DF 10 June 2014 Dear Minister, In December 2013, you commissioned the ACMD to begin a regular review of generic definitions under the Misuse of Drugs Act 1971, with the aim of capturing emerging new psychoactive substances. These drugs are variants of controlled drugs and fall outside the existing scope of the Misuse of Drugs Act 1971. The ACMD has considered evidence available on tryptamines in the context of the Misuse of Drugs Act 1971 and I enclose the Advisory Council’s advice and an expanded definition for tryptamine compounds with this letter. The ACMD’s NPS Committee has firstly reviewed previous research and existing controls to identify those tryptamines now seen to evade the existing controls. The ACMD has also reviewed data provided by the Home Office’s early warning systems and networks, clinical toxicology, prevalence and neuropharmacology in arriving at the expanded generic definition. This expanded generic definition will bring drugs such as alpha-methyltryptamine (AMT) as well as 5-MeO-DALT within the scope of the Misuse of Drugs Act 1971. These are highly potent hallucinogens which act on the 5HT2A receptor, in the same way as LSD. The ACMD therefore recommends that the tryptamines covered by the proposed expanded generic definition in this report, are controlled under the Misuse of Drugs Act (1971) as Class A substances. -
Designer Drugs: a Review
WORLD JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES Chavan et al. World Journal of Pharmacy and Pharmaceutical Sciences SJIF Impact Factor 5.210 Volume 4, Issue 08, 297-336. Review Article ISSN 2278 – 4357 DESIGNER DRUGS: A REVIEW Dr. Suyash Chavan,MBBS*1 and Dr. Vandana Roy2 1MD, Resident Doctor, Department of Pharmacology, Maulana Azad Medical College, New Delhi. 2MD, PhD Professor, Department of Pharmacology, Maulana Azad Medical College, New Delhi. ABSTRACT Article Received on 25 May 2015, Designer drugs‟ are psychoactive substances that mimic the effects of Revised on 16 June 2015, other banned illicit drugs but evade detection by law enforcing Accepted on 07 July 2015 agencies. This is because of modifications in the structure of the original psychoactive molecule. Originally developed as a way to *Correspondence for evade existing drug laws in the late 1960s, the synthesis and use of Author designer drugs has increased dramatically. They are advertised with Dr. Suyash Chavan innocuous names and are sold mostly over the internet, discreet outlets MD, Resident Doctor, Department of and at entertainment clubs. Victims may exhibit symptoms similar to Pharmacology, Maulana the effects of the illegal drug that these synthetic drugs mimic, Azad Medical College, however, the exact culprit drug is not detected due to structural New Delhi. modifications in the new drug. Overdose of these drugs may lead to serious adverse effects that can be life threatening. Understanding the pharmacology and toxicology of these agents is essential to facilitate their detection and to provide better medical care for patients suffering from adverse effects due to their consumption. -
Novel Hallucinogens and Plant-Derived Highs
Novel Hallucinogens and Plant-Derived Highs Emily Dye Forensic Chemist Special Testing and Research Laboratory Drug Enforcement Administration Outline • Hallucinogens • Plant-Derived Highs – 2C Compounds – Kratom – NBOMe Compounds – Fly Agaric Mushrooms – DOX Compounds – Kava Kava – Kanna • Empathogens – Aminoindanes – APDB – APB DEA Special Testing and Research Laboratory Emerging Trends Program 2C Compounds • Psychedelic phenethylamines • Synthesized by Alexander Shulgin – Published in PiHKAL • 27 known compounds – Most common: 2C-C, 2C-B, and 2C-I DEA Special Testing and Research Laboratory Emerging Trends Program 2C Compounds DEA Special Testing and Research Laboratory Emerging Trends Program 2C-B-FLY • Psychedelic phenethylamine • Synthesized by Aaron Monte www.erowid.org DEA Special Testing and Research Laboratory Emerging Trends Program Bromo-DragonFLY • Psychedelic phenethylamine • Synthesized in the lab of David Nichols • Deaths associated with misrepresentation as 2C-B-FLY www.erowid.org DEA Special Testing and Research Laboratory Emerging Trends Program NBOMe Compounds • Hallucinogenic phenethylamines • Synthesized by Heim, et al. • Isomers can be distinguished via RT and MS DEA Special Testing and Research Laboratory Emerging Trends Program Name R1 R2 R3 R4 Name R1 R2 R3 R4 25B-NB2OMe Br OCH3 H H 25N-NB2OMe NO2 OCH3 H H 25B-NB3OMe Br H OCH3 H 25N-NB3OMe NO2 H OCH3 H 25B-NB4OMe Br H H OCH3 25N-NB4OMe NO2 H H OCH3 25C-NB2OMe Cl OCH3 H H 25P-NB2OMe CH2CH2CH3 OCH3 H H 25C-NB3OMe Cl H OCH3 H 25P-NB3OMe CH2CH2CH3 H OCH3 H 25C-NB4OMe -
Pharmacology Notebook 1 PDF (Searchable)
The Shulgin Lab Books December 2012 May 2018 Pharmacology Lab Notes #1 (1960 - 1976) A Bit About This Document: While undertaking the work of investigating the chemistry and pharmacology of many varied psychoactive substances, Alexander “Sasha” Shulgin kept detailed notebooks. His documentation covered not only on his own personal research, but the research of friends and acquaintances. This book, the first of the “Pharmacology” series, represents mostly sub-acute work-ups of various substances and subjective responses by Shulgin and his research group. It covers the time frame of 1960 to 1976. The Creation of This Document: The project to undertake the transcribing of Shulgin’s Lab Books was started in 2008 by a team of volunteers and staff at Erowid, along with members of Team Shulgin. Various books were transcribed without a clear idea of how to present the information as a final product; eventually this format was chosen and a volunteer began work assembling the document. Each page was painstakingly transcribed from scanned images. All the hand-drawn “dirty pictures” (molecule drawings) and graphs were edited from the original scans and combined with drawn-in marks, outlines, and arrows to form this searchable PDF. Most of the names in this document have been redacted and pseudonyms put in their place. Names are presented as much as possible as they were in the original book, for example “Robert Thompson” is also “Robert”, “R.Thompson”, and “RT”. Initials are frequently used, and no two people share names or initials so the reader can keep track of who’s who. Words highlighted in yellow are words that the transcription team could not decipher. -
Mini Review on Psychedelic Drugs: Illumination on the Hidden Aspects of Mind
Review Article Mini Review on Psychedelic Drugs: Illumination on the Hidden Aspects of Mind Lemlem Hussien Salih and Atul Kaushik* Department of Medicinal Chemistry, School of Pharmacy, Asmara College of Health Sciences, Asmara, Eritrea ABSTRACT Psychedelics constitute a class of psychoactive drugs with unique effects on consciousness. Psychedelic means mind/soul "revealing" and refers to the ability of these drugs to illuminate normally hidden aspects of mind or psyche. Many psychedelic agents occur in nature; others are synthetically produced. Naturally occurring psychedelic drugs have been inhaled, ingested, worshiped, and reviled since Address for prehistory. The phenomenology of the hallucinogenic experience is Correspondence extremely complex, sensory, emotional, cognitive, and spiritual, levels. Most psychedelic drugs structurally resemble with Department of neurotransmitters: acetylcholine, two catecholamines (nor Medicinal Chemistry, epinephrine and dopamine), and serotonin. These structural School of Pharmacy, similarities lead to three classes for categorizing psychedelic drugs: Asmara College of anticholinergic, catecholamine-like, and serotonin-like. And also a Health Sciences, fourth class of psychedelic drugs can be included, the psychedelic Asmara, Eritrea anesthetics. This mini review focuses on pharmacological and Tel.- +291-1-186041 medicinal aspects of this class. E-mail: atul_kaushik29 Keywords: Psychedelic drugs, Pharmacological features of @rediffmail.com psychedelic drugs, SAR of psychedelic drugs. INTRODUCTION "Rational consciousness...is but one produced. Naturally occurring psychedelic special type of consciousness, whilst all drugs have been inhaled, ingested, about it, parted from it by the filmiest of worshiped, and reviled since prehistory. screens; there lie potential forms of Native American shamans consumed consciousness entirely different."-William psychedelic plants such as the peyote cactus James. -
Multidisciplinary Association for Psychedelic Studies USSC Testimony Re: MDMA March 15, 2017
Multidisciplinary Association for Psychedelic Studies USSC Testimony re: MDMA March 15, 2017 Rick Doblin, Ph.D., Testimony to US Sentencing Commission Re: MDMA Prepared in collaboration with Ismail L. Ali, JD, and Natalie Lyla Ginsberg, MSW Table of Contents I. The Creation & Criminalization of MDMA ..............................................................2 a. Origin of MDMA..........................................................................................................2 b. History of Criminalization ..........................................................................................3 II. The MDMA Sentencing Guideline Lacks an Empirical Basis .................................5 a. Two federal courts have found the 2001 MDMA Sentencing Guideline to be excessive. .......................................................................................................................5 b. As successfully argued by the ACLU, the present MDMA Sentencing Guideline is based on inaccurate science that exaggerated risks. .............................................6 c. Most commonly-cited MDMA neurotoxicity studies are misleading. ...................10 III. MDMA’s Robust Prosocial Capacity and Low Risk Profile ..................................11 a. MDMA’s Risk Profile ................................................................................................11 b. MDMA literature reviews highlight MDMA’s prosocial capacities .....................12 c. MAPS has sponsored and published FDA-approved drug development studies -
Alarming Trends in a Novel Class of Designer Drugs
linica f C l To o x l ic a o n r l o u g o y J Grane et al. J Clinic Toxicol 2011, 1:2 Journal of Clinical Toxicology DOI: 10.4172/2161-0495.1000108 ISSN: 2161-0495 Research Article Article OpenOpen Access Access Alarming Trends in a Novel Class of Designer Drugs Owen Mc Grane*, Joshua Simmons, Eric Jacobson and Carl Skinner Department of Emergency Medicine, Madigan Army Medical Center, Tacoma, WA, USA Abstract Recent years have shown an increase in the use of the so-called “designer drugs.” This term is usually applied to recreational drugs that are new, synthetic and emerge as unscheduled drugs since they have not been in existence long enough to be illegal. These drugs are usually available at “head shops”, tobacco stores, gas stations and via the internet. Several such classes have gained increasing notoriety in the past 3-4 years, especially Spice and bath salts. One class that has gone almost unrecognized is the 2C class. The 2C’s are a class of synthetic hallucinogens known as phenethylamines, the same class as the naturally occurring drug mescaline. Few case reports of actual overdoses from 2C compounds have been reported, but some of the physical stigmata of use or overdose are thought to be pupil dilation, facial flushing, diaphoresis, bruxism, facial grimacing, tachycardia, tachypnea, emotional lability, and subjective symptoms such as accelerated internal clock, and detachment from surroundings. There are no known screening tests to easily detect the substance. However, it has been shown to be detected in rat urine using gas-chromatographic-mass spectrometry (GM-MS) as well as in human blood plasma using gas chromatography-mass spectrometry (GC-MS) and in human urine by capillary electrophoresis-MS [11,23]. -
Nbomes–Highly Potent and Toxic Alternatives of LSD
fnins-14-00078 February 24, 2020 Time: 17:4 # 1 REVIEW published: 26 February 2020 doi: 10.3389/fnins.2020.00078 NBOMes–Highly Potent and Toxic Alternatives of LSD Jolanta B. Zawilska1*, Monika Kacela1 and Piotr Adamowicz2 1 Department of Pharmacodynamics, Medical University of Łód´z,Łód´z,Poland, 2 Department of Forensic Toxicology, Institute of Forensic Research, Kraków, Poland Recently, a new class of psychedelic compounds named NBOMe (or 25X-NBOMe) has appeared on the illegal drug market. NBOMes are analogs of the 2C family of phenethylamine drugs, originally synthesized by Alexander Shulgin, that contain a N-(2-methoxy)benzyl substituent. The most frequently reported drugs from this group are 25I-NBOMe, 25B-NBOMe, and 25C-NBOMe. NBOMe compounds are ultrapotent and highly efficacious agonists of serotonin 5-HT2A and 5-HT2C receptors (Ki values in low nanomolar range) with more than 1000-fold selectivity for 5-HT2A compared with 5-HT1A. They display higher affinity for 5-HT2A receptors than their 2C counterparts and have markedly lower affinity, potency, and efficacy at the 5- HT2B receptor compared to 5-HT2A or 5-HT2C. The drugs are sold as blotter papers, or in powder, liquid, or tablet form, and they are administered sublingually/buccally, intravenously, via nasal insufflations, or by smoking. Since their introduction in the early 2010s, numerous reports have been published on clinical intoxications and Edited by: Liana Fattore, fatalities resulting from the consumption of NBOMe compounds. Commonly observed Italian National Research Council, Italy adverse effects include visual and auditory hallucinations, confusion, anxiety, panic Reviewed by: and fear, agitation, uncontrollable violent behavior, seizures, excited delirium, and Adam Halberstadt, sympathomimetic signs such mydriasis, tachycardia, hypertension, hyperthermia, and University of California, San Diego, United States diaphoresis. -
Bath Salts Or Methylenedioxypyrovalerone (MDPV)
New Highs for the New Millennium Brandon J. Warrick MD Assistant Clinical Professor Wayne State University Disclosures • No financial disclosures • All treatments mentioned in this talk are FDA approved. • Treatment dosing may exceed package insert Objectives • What are “Bath Salts”? • What is “Spice or K2”? • Epidemiology • Were did designer drugs come from? • Were are designer drugs going? What are “Bath Salts”? Testimonials • “I don’t believe in the hype so I ordered some offline and received in roughly a week and a half. It came in a 250mg package that ran me roughly 18 dollars with tax and shipping included. I tried roughly 10mg and absolutely loved it. Immediately after ingestion of the bath salts I felt a rush of energy and even a slight euphoria to go along with it. My mind felt like it was working in overdrive and I wanted to talk to anyone about anything I possibly could…” • “At about 1 hour and 10 minutes in I got the strongest urge to redose I have ever felt from a drug, including cocaine.” Physical Properties • White to Light Brown • Hydrophilic • Crumbly powder • Slight odor Michigan; How it Began • First call December 18, 2010 • First Death February 3 2011 • February 2-7 10 cases • Reported – Bay City – Iron Wood – Mt. Clemons PCC & Health Department Need PCC MDCH 24/7 Call Center Yes No Able to give medical advice Yes No Real-time reporting Yes Yes Able to mandate reporting No Yes Able to take legal action No Yes Able to create EPI-X alerts* Yes Yes Able to create HAN* No Yes Able to submit MMWR* No Yes Participates in -
[(2-Methoxyphenyl) Methyl]Ethanamine Derivatives on Blotter Paper
journal of Analytical Toxicology 2015;39:617-623 doi,10.1093/jar/bkv073 Special Issue Analysis of 251-NBOMe, 25B-NBOMe, 25C~NBOMe and Other Dimethoxyphenyl-N-[(2-Methoxyphenyl) Methyl]Ethanamine Derivatives on Blotter Paper Justin L. Poklisl, Stephen A.Raso-, Kylie N. Alford", Alphonse Poklis1.2,3 and Michelle R. Peace?" 'Department of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond, VA,USA,zDepartment of Forensic Science, Virginia Commonwealth University, PO Box 843079,1015 Floyd Avenue, Room 2015, Richmond 23284, VA,USA,and 3Department of Pathology, Virginia Commonwealth University, Richmond, VA,USA •Authorto whom correspondence should be addressed.Email:[email protected] In recent years, N-methoxybenzyl-methoxyphenylethylamine (NBOMe) methoxybenzyl)ethanamine (25E-NBOMe), 2-(2,5-dimethoxy- derivatives, a class of designer hallucinogenic drugs, have become 3,4 dimethylphenyl)-1V-(2-methoxybenzyl)ethanamine (25G- popular drugs of abuse. These drugs have been the cause of severe l\'BOMe), N(2-methoxybenzyl)-2,5·dimethoxy-4-chlorophene- intoxications and even deaths. They act as S-HT2A receptors agonists thylamine (25C-NBOMe) and 2-(4-iodo-2,5-dirnethoxyphenyl)- and have been reported to produce serotonin-like syndrome with bi- N[(2,3-methylenedioxyphenyl) methyl]ethanamine (25I-l\TBMD) zarre behavior, severe agitation and seizures persisting for as long (9-i 1). as 3 days. The most commonly reported derivatives are 2SI-NBOMe, Several publisbed abstracts and clinical case reports have de- 2SB-NBOMe and 2SC-NBOMe, respectively 2-(4-iodo-2,S-dimethoxy- scribed signs and symptoms of 25I-NBOMe (1, s, 12-1(;), phenyl)-N-[(2-methoxyphenyl) methyljethanamine, N-(2-methoxyben- 25B-l\'BOMe (17-20) and 25C-NBOMe (W-Zl) intoxication. -
2C-P Monograph
Emerging Designer Drug Monograph Revision Date: February 12, 2014 Author(s): Victor Uralets Drug Name: 2C-P Synonyms: 2-(2,5-Dimethoxy-4-propylphenyl)ethanamine; 2,5-dimethoxy-4-(n)- propylphenethylamine Structure: Formula: C13H21NO2 Molecular Weight: 223.3 Pharmacological drug class: 2C-P belongs to a family of 4-substituted 2,5- dimethoxyphenylethylamines (2C- drugs), first synthesized and tested by Alexander Shulgin (1). 2C- P was described as the most potent psychedelic drug in the entire 2C- family with pronounced hallucinogenic effect (1). It was also found difficult to establish an effective and safe dose for the drug (1). Metabolism: In spite of the lack of data on 2C-P metabolism, reasonable predictions could be made on the basis of the known pathways (2) for the analogs: 2C-D (3), 2C-E (4), 2C-I (5) and 2C-B (6- 10). All of them undergo the following metabolic steps in animal (mice, rat) and in vitro studies: O- demethylation in positions 2 and 5, N-acetylation, β-hydroxylation (two diastereomers for each), deamination with subsequent oxidation to carboxylic acid or reduction to alcohol. 2C-D and 2C-E, the most closely related analogs to 2C-P, were also found (3, 4) to metabolize by hydroxylation (followed by carboxylation) in the alkyl radical located in position 4. 2C-P would likely follow the same path. Metabolites are excreted in urine mostly as conjugates. A recent study of 2C-B metabolism in human (11) found, that the major path was oxidative deamination. The main products in urine were: 4-bromo-2,5-dimethoxyphenylacetic acid (73%), 4- bromo-2-hydroxy,5-methoxyphenylacetic acid (13%) and 4-bromo-2,5-dimethoxyphenylethyl alcohol (4.5%).