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DOI: 10.1055/s-0035-1562781
New Acyloxymethyl Ketones: Useful Probes for Cysteine Protease Profiling
Publication History
Received: 26 April 2016
Accepted after revision: 18 June 2016
Publication Date:
29 July 2016 (online)
§ These authors contributed equally to this work
Abstract
Peptidyl-acyloxymethyl ketones (AOMKs) belong to a class of selective, irreversible inhibitors (activity-based probes) widely used as chemical tools of investigating proteins, for example, in activity-based protein profiling. The synthesis of the AOMKs has always been challenging and current methodologies involve both solution and solid-phase synthesis. Herein, the synthesis of a new scaffold useful for the preparation of peptidyl-AOMKs is reported and it is demonstrated that the new synthetic probes bearing a 4-functionalized 2,6-dimethylbenzoate efficiently inhibit cysteine proteases like cathepsin B.
Key words
acyloxymethyl ketones - activity-based probes - peptidyl-AOMKs - 2,6-dimethylbenzoates - solid-phase peptide synthesisSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1562781.
- Supporting Information
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