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Webinars
Benzodiazepines were discovered in the 1950s and were rapidly adopted as prescription medicines for the treatment of a variety of conditions, such as anxiety or use as sedatives. However, the increase in popularity of benzodiazepines, along with their addictive properties, also led to an increase in the misuse and abuse of these compounds.
In this presentation, Kirk Hering, Director of Process Exploration and Psychoactive Substance Chemistry at Cayman Chemical, reviews the known metabolic pathways of established designer benzodiazepines and discusses the metabolites likely to form from emerging NPS ethyltriazolobenzodiazepines.
Presented as part of the CFSRE's 2026 Current Trends in Forensic Toxicology Symposium.
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Novel designer benzodiazepines (DBZD) and novel synthetic opioids (NSO) continue to emerge on the illicit novel psychoactive substance (NPS) market. Given this trend, and the continuing rise in benzodiazepine prescriptions, the likelihood for benzodiazepines to appear in toxicological samples alongside synthetic opioids is high. Understanding the synthesis and analytical interpretation of both NPS classes can help prepare forensic toxicologists for the appearance of unknown compounds in their casework.
Join Nathan Layle and Becca Boyce, synthetic organic chemists at Cayman Chemical, as they present the results of our in-house human liver microsome (HLM) studies and demonstrate how these findings can be applied to new analogs. Attendees will gain insights into emerging compounds and metabolites that may soon appear in forensic casework.
Presented as part of the CFSRE's 2026 Current Trends in Forensic Toxicology Symposium.
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Mitragynine is an indole-based alkaloid and is one of the main psychoactive constituents in the Southeast Asian plant Mitragyna speciosa, commonly known as kratom. It is an atypical opioid that is typically consumed as a part of kratom for its pain-relieving and euphoric effects and has also been researched for its use to potentially manage symptoms of opioid withdrawal and as a treatment for alcohol use disorder (AUD). More recently, analogs of mitragynine have begun to appear in the unregulated consumer marketplace and some are readily available in gas stations and vape shops in products branded as "7-hydroxymitragynine" or "7OH" causing heightened concern due to studies showing that 7-hydroxy mitragynine and mitragynine pseudoindoxyl (the rearrangement product of 7-hydroxy mitragynine) are more potent opioid agonists, exceeding that of mitragynine on the order of 10x and 100x, respectively.
Listen as Nathan Layle and Camille Waston-Gooden, synthetic chemists at Cayman Chemical, explain more about the history, pharmacology, metabolism, semi-synthetic modifications, and new emerging analogs of Mitragynine.
Presented as part of the CFSRE's 2026 Current Trends in Seized Drug Analysis Symposium.
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Semi-synthetic cannabinoids (SSCs) represent an emerging class of Novel Psychoactive Substances (NPSs) that are often advertised and sold as legal. SSCs can be described as partially synthetic materials that are derived from natural components of the Cannabis Sativa L. plant, such as Cannabidiol (CBD). New studies on the in-vivo and in-vitro metabolism of SSC’s, such as Δ10-THC, Δ6a,10a-THC, and HHC, are emerging, which detail the similarities and differences seen to natural phytocannabinoid like Δ9-THC.
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Following China's generic structural class ban of several sub-classes of synthetic cannabinoids in 2021, the NPS/designer-drug landscape continues to evolve to evade regulation. As new structural variations appear on the grey market, another new phenomenon is the emergence of 'DIY' semi-finished kits. These semi-finished kits provide the end-user with non-regulated precursors enabling the user to finish the synthesis themselves to the desired synthetic cannabinoid of choice. Because the end-user often does not have the appropriate engineering and quality controls in place, drug substances on the illicit market are commonly contaminated with unreacted chemical precursors. Several of these tail-less penultimate precursors have been detected on the grey market since late 2021.
Listen in as Holly Pierzynski, Cayman's Manager of Forensic Novel Psychoactive Substance Research, discusses several emerging synthetic cannabinoids, their precursors, synthesis, and byproducts from the synthesis. This presentation also highlights Cayman's new application note, "GC Separation of ADB-BUTINACA from its precursor ADB-INACA".
Presented as part of the 2024 Midwestern Association of Forensic Scientists Conference in Kansas City, Missouri.
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Ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) suppresses innate immunity and promote tumor progression and metastasis in the tumor microenvironment. ENPP1 inhibits STING signaling by hydrolyzing the degradation of 2',3'-cGAMP, blunting induction of the type 1 interferon response and antitumor immunity.
Listen as David Taylor, Ph.D., a scientist in Cayman's Assay Research & Development group, modulates ENPP1 expression and STING activation in ovarian cancer cell lines and macrophages with LipidLaunch™ Loadable LNPs and explores the contribution of ovarian cancer cell-derived extracellular vesicles in the tumor microenvironment.
Presented as part of the 2024 Tumor Microenvironment and Therapy Symposium at The University of Michigan.
Read the Webinar Highlights for a quick overview of the key takeaways.
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Listen as Julie Rumble, PhD, Director of Immunology Services at Cayman Chemical, discusses the workflow for formulation, analysis, and testing of LNPs in multiple cell types.
Presented by Unchained Labs and Fierce Biotech.
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The Magic and Chemistry Behind Psychedelic Mushrooms
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Cayman Chemical
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Cayman Chemical1180 East Ellsworth RoadAnn Arbor, Michigan 48108 USA