Download Product Insert (PDF)

Total Page：16

File Type：pdf, Size：1020Kb

PRODUCT INFORMATION ADB-PINACA Item No. ISO00150 CAS Registry No.: 1633766-73-0 Formal Name: N-[1-(aminocarbonyl)-2,2-dimethylpropyl]-1- pentyl-1H-indazole-3-carboxamide N MF: C19H28N4O2 O N FW: 344.5 O Purity: ≥98% N Supplied as: A neat solid H NH2 Storage: -20°C Stability: ≥3 years Information represents the product specifications. Batch specific analytical results are provided on each certificate of analysis. Description ADB-PINACA (Item No. ISO00150) is an analytical reference material categorized as a synthetic cannabinoid.1 ADB-PINACA is regulated as a Schedule I compound in the United States. This product is intended for research and forensic applications. This product is qualified as a Reference Material that has been manufactured and tested to ISO/IEC 17025 and ISO 17034 international standards. Reference 1. Banister, S.D., Moir, M., Stuart, J., et al. Pharmacology of indole and indazole synthetic cannabinoid designer drugs AB-FUBINACA, ADB-FUBINACA, AB-PINACA, ADB-PINACA, 5F-AB-PINACA, 5F-ADB- PINACA, ADBICA, and 5F-ADBICA. ACS Chem. Neurosci. 6(9), 1546-1559 (2015). WARNING CAYMAN CHEMICAL THIS PRODUCT IS FOR RESEARCH ONLY - NOT FOR HUMAN OR VETERINARY DIAGNOSTIC OR THERAPEUTIC USE. 1180 EAST ELLSWORTH RD SAFETY DATA ANN ARBOR, MI 48108 · USA This material should be considered hazardous until further information becomes available. Do not ingest, inhale, get in eyes, on skin, or on clothing. Wash thoroughly after handling. Before use, the user must review the complete Safety Data Sheet, which has been sent via email to your institution. PHONE: [800] 364-9897 WARRANTY AND LIMITATION OF REMEDY [734] 971-3335 Buyer agrees to purchase the material subject to Cayman’s Terms and Conditions. Complete Terms and Conditions including Warranty and Limitation of Liability information can be found on our website. FAX: [734] 971-3640 [email protected] Copyright Cayman Chemical Company, 07/15/2019 WWW.CAYMANCHEM.COM.

Copy Link

Recommended publications

Recommended Methods for the Identification and Analysis of Synthetic Cannabinoid Receptor Agonists in Seized Materials (Revised and Updated)
Recommended methods for the Identification and Analysis of Synthetic Cannabinoid Receptor Agonists in Seized Materials (Revised and updated) MANUAL FOR USE BY NATIONAL DRUG ANALYSIS LABORATORIES Photo credits: UNODC Photo Library; UNODC/Ioulia Kondratovitch; Alessandro Scotti. Laboratory and Scientific Section UNITED NATIONS OFFICE ON DRUGS AND CRIME Vienna Recommended Methods for the Identification and Analysis of Synthetic Cannabinoid Receptor Agonists in Seized Materials (Revised and updated) MANUAL FOR USE BY NATIONAL DRUG ANALYSIS LABORATORIES UNITED NATIONS Vienna, 2020 Note Operating and experimental conditions are reproduced from the original reference materials, including unpublished methods, validated and used in selected national laboratories as per the list of references. A number of alternative conditions and substitution of named commercial products may provide comparable results in many cases, but any modification has to be validated before it is integrated into laboratory routines. Mention of names of firms and commercial products does not imply theendorsement of the United Nations. ST/NAR/48/REV.1 © United Nations, July 2020. All rights reserved, worldwide The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. This publication has not been formally edited. Publishing production: English, Publishing and Library Section, United Nations Office at Vienna. Acknowledgements The Laboratory and Scientific Services of the United Nations Office on Drugs and Crime (UNODC) (LSS, headed by Dr.
[Show full text]
Synthetic Cannabinoids Synthetic Cannabinoids-1
Synthetic Cannabinoids-1 Synthetic Cannabinoids ™ (HEIA ) For the detection of JWH-018, JWH-073, AM-2201 & their major metabolites Homogeneous Enzyme Immunoassay (HEIA™) K2-3 K2-2 K2-1 Assay Specifications Sensitivity: 100% LC-MS/MS Confirmation Specificity: 87.5% Methodology: Homogeneous Enzyme Immunoassay Accuracy: 96.9% Positive Negative Cutoff: 10 ng/mL HEIA Positive 48 2* Calibrator: JWH-018 N-pentanoic acid (10 ng/mL) Negative 0 14 *2 discrepant specimens that screened negative were borderline negative at 10 ng/mL cutoff. AB-PINACA ADB-PINACA UR-144 XLR11 JWH-018 JWH-073 AM-2201 Immunalysis now offers three distinct Synthetic Cannabinoid Homogeneous Enzyme Immunoassays (HEIA™) Cross-Reactivity N/D = Cross-Reactivity < 0.05% for the detection of Synthetic Cannabinoids in urine. Our assays, geared towards the detection of JWH-018, JWH-073, AM-2201, UR-144, XLR11 and their metabolites, are now complemented by a NEW assay targeted Analyte Analyte Concentration JWH-018 N-pentanoic acid Cross-Reactivity at the next generation, AB-PINACA and ADB-PINACA compounds found in the current Spice or K2 products. (ng/mL) Equivalent (ng/mL) (%) Together, these assays detect Schedule I controlled substances and provide the most comprehensive screening JWH-018 N-pentanoic acid 10 10 100 tool for your automated chemistry analyzer. JWH-018 N-(5-hydroxypentyl) 15 10 67 JWH-018 4-hydroxyindole 135 10 7.4 JWH-018 5-hydroxyindole 40 10 25 AM-2201 N-(4-hydroxypentyl) 12 10 83 Liquid Stable, Ready to Use AM-2201 6-hydroxyindole 20 10 50 JWH-073 N-(4-hydroxybutyl)
[Show full text]
Retrospective Identification of Synthetic Cannabinoids in Forensic Toxicology Casework Using Archived High Resolution Mass Spectrometry Data Author(S): Alex J
The author(s) shown below used Federal funding provided by the U.S. Department of Justice to prepare the following resource: Document Title: Retrospective Identification of Synthetic Cannabinoids in Forensic Toxicology Casework using Archived High Resolution Mass Spectrometry Data Author(s): Alex J. Krotulski, Ph.D., Amanda L.A. Mohr, MSFS, D-ABFT-FT, Barry K. Logan, Ph.D., F-ABFT Document Number: 255668 Date Received: November 2020 Award Number: 2017-R2-CX-0021 This resource has not been published by the U.S. Department of Justice. This resource is being made publically available through the Office of Justice Programs’ National Criminal Justice Reference Service. Opinions or points of view expressed are those of the author(s) and do not necessarily reflect the official position or policies of the U.S. Department of Justice. Title: Retrospective Identification of Synthetic Cannabinoids in Forensic Toxicology Casework using Archived High Resolution Mass Spectrometry Data Authors: Alex J Krotulski, PhD, Amanda LA Mohr, MSFS, D-ABFT-FT, and Barry K Logan, PhD, F-ABFT Organization: Center for Forensic Science Research and Education at the Fredric Rieders Family Foundation, Willow Grove, PA, USA Award Number: 2017-R2-CX-0021 This resource was prepared by the author(s) using Federal funds provided by the U.S. Department of Justice. Opinions or points of view expressed are those of the author(s) and do not necessarily reflect the official position or policies of the U.S. Department of Justice. Abstract Since 2008, synthetic cannabinoids have continued to proliferate and challenge the forensic science community due to rapid appearance and diverse chemistry.
[Show full text]
How Present Synthetic Cannabinoids Can Help Predict Symptoms in the Future
MOJ Toxicology Mini Review Open Access How present synthetic cannabinoids can help predict symptoms in the future Abstract Volume 2 Issue 1 - 2016 New synthetic cannabinoids appear regularly in the illicit drug market, often in response to Melinda Wilson-Hohler,1 Wael M Fathy,2 legal restrictions. These compounds are characterized by increasing binding affinities (Ki) 3 to CB1 and CB2 receptors. Increasing affinity to CB receptors can occur by substitution of a Ashraf Mozayani 1Consultant, The Forensic Sciences, USA halogen on the terminal position of the pentyl chain of the classical synthetic cannabinoids. 2Post-Doctoral Fellowship, Texas Southern University, USA & Fluorination of the aliphatic side chain of established cannabinoid agonists is a popular Toxicologist, Ministry of Justice, Egypt pathway of modifying existing active drugs and synthesizing novel drugs to increase 3Professor, Barbara Jordan-Mickey Leland School of Public potency. Biological impacts of these compounds that have been reported include seizures, Affairs, Texas Southern University, USA body temperature losses that may lead to cardiac distress, as well as cases reporting delirium and severe neural incapacities. These symptoms have been reported in case Correspondence: Ashraf Mozayani, Executive Director of reports with evidence that like their cannabinoid counterparts, these compounds distribute Forensic Science and Professor, Barbara Jordan-Mickey Leland post-mortem into a variety of tissues, especially adipose tissue. Researchers have detected School of Public Affairs, Texas Southern University, USA, and identified certain synthetic cannabinoid compounds on botanicals using a variety of Tel17132526556, Email [email protected] separation and detection systems such as GC-FID and GC-MS, as well as LC-MS/MS and NMR.
[Show full text]
Cannabinoid-Like Effects of Five Novel Carboxamide Synthetic Cannabinoids T ⁎ Michael B
Neurotoxicology 70 (2019) 72–79 Contents lists available at ScienceDirect Neurotoxicology journal homepage: www.elsevier.com/locate/neuro Full Length Article Cannabinoid-like effects of five novel carboxamide synthetic cannabinoids T ⁎ Michael B. Gatch , Michael J. Forster Department of Pharmacology and Neuroscience, Center for Neuroscience Discovery, University of North Texas Health Science Center, 3500 Camp Bowie Blvd, Fort Worth, TX, 76107-2699, USA ARTICLE INFO ABSTRACT Keywords: A new generation of novel cannabinoid compounds have been developed as marijuana substitutes to avoid drug Drug discrimination control laws and cannabinoid blood tests. 5F-MDMB-PINACA (also known as 5F-ADB, 5F-ADB-PINACA), MDMB- Locomotor activity CHIMICA, MDMB-FUBINACA, ADB-FUBINACA, and AMB-FUBINACA (also known as FUB-AMB, Rat MMB-FUBINACA) were tested for in vivo cannabinoid-like effects to assess their abuse liability. Locomotor Mouse activity in mice was tested to screen for locomotor depressant effects and to identify behaviorally-active dose Abuse liability ranges and times of peak effect. Discriminative stimulus effects were tested in rats trained to discriminate Δ9- tetrahydrocannabinol (3 mg/kg, 30-min pretreatment). 5F-MDMB-PINACA (ED50 = 1.1 mg/kg) and MDMB- CHIMICA (ED50 = 0.024 mg/kg) produced short-acting (30 min) depression of locomotor activity. ADB-FUBINACA (ED50 = 0.19 mg/kg), and AMB- FUBINACA (ED50 = 0.19 mg/kg) depressed locomotor activity for 60–90 min; whereas MDMB-FUBINACA (ED50 = 0.04 mg/kg) depressed locomotor activity for 150 min. AMB-FUBINACA produced tremors at the highest dose tested. 5F-MDMB-PINACA (ED50 = 0.07), MDMB- CHIMICA (ED50 = 0.01 mg/kg), MDMB-FUBINACA (ED50 = 0.051 mg/kg), ADB-FUBINACA (ED50 = 0.075 mg/ 9 kg) and AMB-FUBINACA (ED50 = 0.029) fully substituted for the discriminative stimulus effects of Δ -THC following 15-min pretreatment.
[Show full text]
Classes and Structures of Emerging Cannabimimetics and Cathinones
Classes and Structures of Emerging Cannabimimetics and Cathinones Arthur Berrier Senior Research Chemist Special Testing and Research Laboratory Drug Enforcement Administration Herbal Smoking Blends - SPICE • SPICE and other herbal blends have been sold in head shops and on the Internet since 2006 for their cannabis-like intoxication • The herbal blends sometimes have a fragrance which could include vanilla, potpourri, spice, blueberry, caramel, and strawberry • The plant materials for the different blends have a wide variation in appearance DEA Special Testing and Research Laboratory Emerging Trends Program Herbal Smoking Blends - SPICE • In late 2008, THC Pharma reported the presence of JWH 018, a synthetic cannabimimetic indole in some blends • In early 2009, analogues of CP 47,497 (another synthetic cannabinoid) were also found in some blends by the U. of Freiburg • In early 2009, several European Countries control Herbal Blends/JWH 018/CP 47,497 DEA Special Testing and Research Laboratory Emerging Trends Program Herbal Smoking Blends - SPICE • K2 enters market in April, 2009 • Interest booms in herbal smoking blends in 2009 • Many new products appeared, typically with JWH 018 and JWH 073 • States begin to control the blends/synthetic cannabinoids DEA Special Testing and Research Laboratory Emerging Trends Program Herbal Smoking Blends - SPICE • Products quickly reformulated with new, non- controlled synthetic cannabimimetics • Five of the synthetic cannabimimetics controlled at the Federal level in 2011 • Synthetic Drug Abuse Prevention
[Show full text]
Download Product Insert (PDF)
PRODUCT INFORMATION ADB-PINACA-d9 Item No. 15112 Formal Name: N-(1-amino-3,3-dimethyl-1-oxobutan- 2-yl)-1-(pentyl-2,2’,3,3’,4,4’,5,5,5-d9)- D D D D N 1H-indazole-3-carboxamide O D N MF: C19H19D9N4O2 D O D D D FW: 353.5 N Purity: ≥98% H NH2 Supplied as: A neat solid Storage: -20°C Stability: ≥6 years Information represents the product specifications. Batch specific analytical results are provided on each certificate of analysis. Description ADB-PINACA-d9 (Item No. 15112) is an analytical reference material intended for use as an internal standard for the quantification of ADB-PINACA (Item Nos. ISO00150 | ISO60212) by GC- or LC-MS. The accuracy of the sample weight in this vial is between 5% over and 2% under the amount shown on the vial. If better precision is required, the deuterated standard should be quantitated against a more precisely weighed unlabeled standard by constructing a standard curve of peak intensity ratios (deuterated versus unlabeled). 1 ADB-PINACA is categorized as a synthetic cannabinoid. ADB-PINACA-d9 is regulated as a Schedule I compound in the United States. This product is intended for research and forensic applications. This product is qualified as a Reference Material that has been manufactured and tested to ISO/IEC 17025 and ISO 17034 international standards for reference materials. Reference 1. Banister, S.D., Moir, M., Stuart, J., et al. Pharmacology of indole and indazole synthetic cannabinoid designer drugs AB-FUBINACA, ADB-FUBINACA, AB-PINACA, ADB-PINACA, 5F-AB-PINACA, 5F-ADB- PINACA, ADBICA, and 5F-ADBICA.
[Show full text]
Cardiovascular Effects of Marijuana and Synthetic Cannabinoids: the Good, the Bad, and the Ugly
REVIEWS PREVENTION OF CVD Cardiovascular effects of marijuana and synthetic cannabinoids: the good, the bad, and the ugly Pal Pacher1, Sabine Steffens2, György Haskó3, Thomas H. Schindler4 and George Kunos5 Abstract | Dysregulation of the endogenous lipid mediators endocannabinoids and their G‑protein‑coupled cannabinoid receptors 1 and 2 (CB1R and CB2R) has been implicated in a variety of cardiovascular pathologies. Activation of CB1R facilitates the development of cardiometabolic disease, whereas activation of CB2R (expressed primarily in immune cells) exerts anti-inflammatory effects. The psychoactive constituent of marijuana, Δ9-tetrahydrocannabinol (THC), is an agonist of both CB1R and CB2R, and exerts its psychoactive and adverse cardiovascular effects through the activation of CB1R in the central nervous and cardiovascular systems. The past decade has seen a nearly tenfold increase in the THC content of marijuana as well as the increased availability of highly potent synthetic cannabinoids for recreational use. These changes have been accompanied by the emergence of serious adverse cardiovascular events, including myocardial infarction, cardiomyopathy, arrhythmias, stroke, and cardiac arrest. In this Review, we summarize the role of the endocannabinoid system in cardiovascular disease, and critically discuss the cardiovascular consequences of marijuana and synthetic cannabinoid use. With the legalization of marijuana for medicinal purposes and/or recreational use in many countries, physicians should be alert to the possibility
[Show full text]
ARK™ AB-PINACA Assay
3 SUMMARY AND EXPLANATION OF THE TEST Synthetic cannabinoids are part of a group of drugs called new psychoactive substances (NPS), which are designer drugs intended to mimic the effects of illicit drugs. These substances are called cannabinoids because they interact with the same CB1 and CB2 cannabinoid receptors as tetrahydrocannabinol (THC), the main psychoactive ingredient in marijuana. For Export Only – Not For Sale in USA Although synthetic cannabinoids are functionally similar to THC, many of these substances are not structurally related to THC. Synthetic cannabinoids became popular under the brand names “Spice” and “K2”, in part due to their ability to escape detection by standard cannabinoid screening tests. Synthetic cannabinoids are marketed under a wide variety of speciﬁc brand ™ ARK AB-PINACA Assay names, including Joker, Black Mamba, Kush, and Kronic. Synthetic cannabinoids are used This ARK Diagnostics, Inc. package insert for the ARK AB-PINACA Assay must be read prior in a variety of ways, with the most common method being sprayed onto dried plant material to use. Package insert instructions must be followed accordingly. The assay provides a simple and smoked. Potential adverse effects of synthetic cannabinoid use include anxiety, agitation, and rapid analytical screening procedure for detecting AB-PINACA and its metabolites in hallucinations, dizziness, seizures, rapid heart rate and vomiting.1-9 urine. Reliability of the assay results cannot be guaranteed if there are any deviations from the 4 PRINCIPLES OF THE PROCEDURE instructions in this package insert. The ARK AB-PINACA Assay is a homogeneous enzyme immunoassay method used for the analysis of drug in human urine.
[Show full text]
Critical Review Report: ADB-FUBINACA
Critical Review Report: ADB-FUBINACA Expert Committee on Drug Dependence Forty-first Meeting Geneva, 12-16 November 2018 This report contains the views of an international group of experts, and does not necessarily represent the decisions or the stated policy of the World Health Organization 41st ECDD (2018): ADB-FUBINACA © World Health Organization 2018 All rights reserved. This is an advance copy distributed to the participants of the 41st Expert Committee on Drug Dependence, before it has been formally published by the World Health Organization. The document may not be reviewed, abstracted, quoted, reproduced, transmitted, distributed, translated or adapted, in part or in whole, in any form or by any means without the permission of the World Health Organization. The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted and dashed lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. The World Health Organization does not warrant that the information contained in this publication is complete and correct and shall not be liable for any damages incurred as a result of its use.
[Show full text]
Molecular Pharmacology of Synthetic Cannabinoids: Delineating CB1 Receptor-Mediated Cell Signaling
International Journal of Molecular Sciences Review Molecular Pharmacology of Synthetic Cannabinoids: Delineating CB1 Receptor-Mediated Cell Signaling Kenneth B. Walsh * and Haley K. Andersen Department of Pharmacology, Physiology & Neuroscience, University of South Carolina, School of Medicine, Columbia, SC 29208, USA; [email protected] * Correspondence: [email protected] Received: 24 July 2020; Accepted: 14 August 2020; Published: 25 August 2020 Abstract: Synthetic cannabinoids (SCs) are a class of new psychoactive substances (NPSs) that exhibit high affinity binding to the cannabinoid CB1 and CB2 receptors and display a pharmacological profile similar to the phytocannabinoid (-)-trans-D9-tetrahydrocannabinol (THC). SCs are marketed under brand names such as K2 and Spice and are popular drugs of abuse among male teenagers and young adults. Since their introduction in the early 2000s, SCs have grown in number and evolved in structural diversity to evade forensic detection and drug scheduling. In addition to their desirable euphoric and antinociceptive effects, SCs can cause severe toxicity including seizures, respiratory depression, cardiac arrhythmias, stroke and psychosis. Binding of SCs to the CB1 receptor, expressed in the central and peripheral nervous systems, stimulates pertussis toxin-sensitive G proteins (Gi/Go) resulting in the inhibition of adenylyl cyclase, a decreased opening of N-type Ca2+ channels and the activation of G protein-gated inward rectifier (GIRK) channels. This combination of signaling effects dampens neuronal activity in both CNS excitatory and inhibitory pathways by decreasing action potential formation and neurotransmitter release. Despite this knowledge, the relationship between the chemical structure of the SCs and their CB1 receptor-mediated molecular actions is not well understood.
[Show full text]
Tripping with Synthetic Cannabinoids (“Spice”): Anecdotal and Experimental Observations in Animals and Man
Tripping with Synthetic Cannabinoids (“Spice”): Anecdotal and Experimental Observations in Animals and Man Torbjorn€ U.C. Ja¨rbe and Jimit Girish Raghav Abstract The phenomenon of consuming synthetic cannabinoids (“Spice”) for recreational purposes is a fairly recent trend. However, consumption of cannabis dates back millennia, with numerous accounts written on the experience of its consumption, and thousands of scientiﬁc reports published on the effects of its constituents in laboratory animals and humans. Here, we focus on consolidating the scientiﬁc literature on the effects of “Spice” compounds in various behavioral assays, including assessing abuse liability, tolerance, dependence, withdrawal, and potential toxicity. In most cases, the behavioral effects of “Spice” compounds are compared with those of Δ9-tetrahydrocannabinol. Methodological aspects, such as modes of administration and other logistical issues, are also discussed. As the original “Spice” molecules never were intended for human consumption, scientif- ically based information about potential toxicity and short- and long-term behav- ioral effects are very limited. Consequently, preclinical behavioral studies with “Spice” compounds are still in a nascent stage. Research is needed to address the addiction potential and other effects, including propensity for producing tissue/ organ toxicity, of these synthetic cannabimimetic “Spice” compounds. Keywords Cannabinoid • Cannabinoid receptor 1 • Marijuana • ‘Spice’ • Synthetic marijuana • THC Contents 1 The Cannabis Plant ......................................................................... 264 2 Personal Testimonies ....................................................................... 265 3 Synthetic Cannabinoids ..................................................................... 265 T.U.C. Ja¨rbe (*) and J.G. Raghav Department of Pharmaceutical Sciences, Center for Drug Discovery (CDD), Northeastern University, 116 Mugar Hall, 360 Huntington Ave, Boston, MA 02115, USA e-mail: [email protected] 264 T.U.C.
[Show full text]