Bike peptides: a ride through the membrane.
JOURNAL OF PEPTIDE SCIENCE(2017)
摘要
Several natural peptides have a biaryl or biaryl ether motif in their biologically active structures. A model bicyclic pentapeptide containing a biaryl bridge has been synthesized by solid-phase peptide synthesis combining on-resin Suzuki and Miyaura cross-coupling reactions. Its biological properties in terms of permeability, stability and cytotoxicity have been studied, demonstrating the positive contribution of the biaryl bridge, excellent membrane penetration and serum stability Copyright (c) 2017 European Peptide Society and John Wiley & Sons, Ltd.
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关键词
solid-phase peptide synthesis,stapled peptides,Suzuki cross-coupling,borylation,head-to-tail cyclization,PAMPA,biostability
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