Journal of the American Chemical Society · 2019 · 68 citations · 12 references
PharmacyBiochemistryMedicinal ChemistryBiocatalysisDrug DiscoveryNatural Product BiosynthesisAlkaloid BiosynthesisNatural Product Drug DiscoveryPlant Natural Product BiosynthesisBiocatalytic SynthesisEnzymatic Pathways In Alkaloid BiosynthesisPlant AlkaloidsPlant-derived Natural Products
(-)-Ibogaine and (-)-voacangine are plant derived psychoactives that show promise as treatments for opioid addiction. However, these compounds are produced by hard to source plants, making these chemicals difficult for broad-scale use. Here we report the complete biosynthesis of (-)-voacangine, and de-esterified voacangine, which is converted to (-)-ibogaine by heating, enabling biocatalytic production of these compounds. Notably, (-)-ibogaine and (-)-voacangine are of the opposite enantiomeric configuration compared to the other major alkaloids found in this natural product class. Therefore, this discovery provides insight into enantioselective enzymatic formal Diels-Alder reactions.
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Drug and Opioid-Involved Overdose Deaths — United States, 2013–2017
Lawrence Scholl, Puja Seth, Mbabazi Kariisa et al. · MMWR Morbidity and Mortality Weekly Report · 2018 · 1.8K citations · Full text
Pharmacy, Pharmacology, Toxicology +16
Recent developments in imino Diels–Alder reactions
Paul T. Buonora, John‐Carl Olsen, Taeboem Oh · Tetrahedron · 2001 · 406 citations
Missing enzymes in the biosynthesis of the anticancer drug vinblastine in Madagascar periwinkle
Lorenzo Caputi, Jakob Franke, Scott C. Farrow et al. · Science · 2018 · 395 citations