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Synthesis of the Death-Cap Mushroom Toxin α-Amanitin
- Source :
- Journal of the American Chemical Society. 140:6513-6517
- Publication Year :
- 2018
- Publisher :
- American Chemical Society (ACS), 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 :
- Models, Molecular
endocrine system
animal structures
Molecular Conformation
RNA polymerase II
CHO Cells
010402 general chemistry
medicine.disease_cause
01 natural sciences
Biochemistry
Catalysis
Structure-Activity Relationship
Cricetulus
Colloid and Surface Chemistry
polycyclic compounds
medicine
Animals
Structure–activity relationship
Amanita phalloides
Alpha-Amanitin
Amanitin
Mushroom
Dose-Response Relationship, Drug
Bicyclic molecule
biology
010405 organic chemistry
Toxin
Chemistry
Chinese hamster ovary cell
General Chemistry
Mycotoxins
biology.organism_classification
0104 chemical sciences
biology.protein
Agaricales
Subjects
Details
- ISSN :
- 15205126 and 00027863
- Volume :
- 140
- Database :
- OpenAIRE
- Journal :
- Journal of the American Chemical Society
- Accession number :
- edsair.doi.dedup.....eeb5a291832ff26810ff0e66c42cfa83
- Full Text :
- https://doi.org/10.1021/jacs.7b12698