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Synthesis of the Death-Cap Mushroom Toxin α-Amanitin.

Authors :
Matinkhoo K
Pryyma A
Todorovic M
Patrick BO
Perrin DM
Source :
Journal of the American Chemical Society [J Am Chem Soc] 2018 May 30; Vol. 140 (21), pp. 6513-6517. Date of Electronic Publication: 2018 Mar 21.
Publication Year :
2018

Abstract

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 (2 S,3 R,4 R)-4,5-dihydroxy-isoleucine, and diastereoselective sulfoxidation.

Details

Language :
English
ISSN :
1520-5126
Volume :
140
Issue :
21
Database :
MEDLINE
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
29561592
Full Text :
https://doi.org/10.1021/jacs.7b12698