Synthesis of the Death-Cap Mushroom Toxin α‑Amanitin

α-Amanitin is an extremely toxic bicyclic octapeptide isolated from the death-cap mushroom, Amanita phalloides. As a potent inhibitor of RNA polymerase II, α-amanitin is toxic to eukaryotic cells. Recent interest in α-amanitin arises from its promise as a payload for antibody–drug conjugates. For ov...

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Veröffentlicht in:Journal of the American Chemical Society 2018-05, Vol.140 (21), p.6513-6517
Hauptverfasser: Matinkhoo, Kaveh, Pryyma, Alla, Todorovic, Mihajlo, Patrick, Brian O, Perrin, David M
Format: Artikel
Sprache:eng
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Zusammenfassung:α-Amanitin is an extremely toxic bicyclic octapeptide isolated from the death-cap mushroom, Amanita phalloides. As a potent inhibitor of RNA polymerase II, α-amanitin is toxic to eukaryotic cells. Recent interest in α-amanitin arises from its promise as a payload for antibody–drug conjugates. For over 60 years, A. phalloides has been the only source of α-amanitin. Here we report a synthesis of α-amanitin, which surmounts the key challenges for installing the 6-hydroxy-trypta­thionine sulfoxide bridge, enantio­selective synthesis of (2S,3R,4R)-4,5-dihydroxy-isoleucine, and diastereo­selective sulfoxidation.
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.7b12698