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Solid-phase synthesis of succinylhydroxamate peptides: functionalized matrix metalloproteinase inhibitors.

Organic letters (2006-04-07)
Michiel A Leeuwenburgh, Paul P Geurink, Theo Klein, Henk F Kauffman, Gijs A van der Marel, Rainer Bischoff, Herman S Overkleeft
RESUMEN

[reaction: see text] A novel solid-phase synthesis strategy toward succinylhydroxamate peptides, using an appropriately protected hydroxamate building block, is described. Rapid and efficient access is gained to amine-functionalized peptides, which can be decorated with, for instance, a fluorescent label. In addition, we demonstrate an on-resin synthesis of a biotinylated photoactivatable hydroxamate peptide, which can be used as an activity-based probe for matrix metalloproteinases and ADAMs.

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Sigma-Aldrich
Fmoc-L-Photo-Phe-OH, ≥95%