Back to Search
Start Over
Synthesis of the Death-Cap Mushroom Toxin α-Amanitin.
- 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.
- Subjects :
- Alpha-Amanitin chemistry
Alpha-Amanitin pharmacology
Animals
CHO Cells
Cricetulus
Dose-Response Relationship, Drug
Models, Molecular
Molecular Conformation
Mycotoxins chemistry
Mycotoxins pharmacology
Structure-Activity Relationship
Agaricales chemistry
Alpha-Amanitin chemical synthesis
Mycotoxins chemical synthesis
Subjects
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