期刊
JOURNAL OF MEDICINAL CHEMISTRY
卷 55, 期 24, 页码 10995-11003出版社
AMER CHEMICAL SOC
DOI: 10.1021/jm301443r
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A new class of potent proteasome inhibitors is described, of which the members contain an amino acid inspired sulfonyl fluoride as the electrophilic trap. In total, 24 peptido sulfonyl fluoride inhibitors have been designed and synthesized, which were inspired by the backbone sequences of the proteasome inhibitors bortezomib, epoxomicin, and Cbz-Leu(3)-aldehyde. Nine of them were very potent proteasome inhibitors, the best of which had an IC50 of 7 nM. A number of the peptido sulfonyl fluoride inhibitors were found to be highly selective for the beta 5 proteasome subunit.
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