| Literature DB >> 22374802 |
Jumpei Morimoto1, Yuuki Hayashi, Hiroaki Suga.
Abstract
Designed to inhibit: by using the random nonstandard peptide integrated discovery (RaPID) system, highly potent isoform-selective inhibitors can be identified from a library of nonstandard macrocyclic peptides. These inhibitors, which contain a mechanism-based warhead residue, are active against the human deacetylase SIRT2, with IC(50) values in the low nanomolar region.Entities:
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Year: 2012 PMID: 22374802 DOI: 10.1002/anie.201108118
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336