Concise Chemoenzymatic Total Synthesis and Identification of Cellular Targets of Cepafungin I

The natural product cepafungin I was recently reported to be one of the most potent covalent inhibitors of the 20S proteasome core particle through a series of in vitro activity assays. Here, we report a short chemoenzymatic total synthesis of cepafungin I featuring the use of a regioselective enzym...

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Veröffentlicht in:Cell chemical biology 2020-10, Vol.27 (10), p.1318-1326.e18
Hauptverfasser: Amatuni, Alexander, Shuster, Anton, Adibekian, Alexander, Renata, Hans
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Sprache:eng
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