| Literature DB >> 32146413 |
Anja Vogelmann1, Dina Robaa2, Wolfgang Sippl2, Manfred Jung3.
Abstract
Proteolysis targeting chimeras (PROTACs) are heterobifunctional molecules and allow selective protein degradation by addressing the natural ubiquitin proteasome system. As this new strategy of chemically induced protein degradation can serve as a biological tool and provides new possibilities for drug discovery, it has been applied to a variety of targets including (nuclear) receptors, kinases, and epigenetic proteins. A lot of PROTACs have already been designed in the field of epigenetics, and their synthesis and characterization highly contributed to structural optimization and improved mechanistic understanding of these molecules. In this review, we will discuss and summarize recent advances in PROTAC discovery with focus on epigenetic targets.Keywords: Drug discovery; Epigenetics; PROTACs; Protein degradation
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Year: 2020 PMID: 32146413 DOI: 10.1016/j.cbpa.2020.01.010
Source DB: PubMed Journal: Curr Opin Chem Biol ISSN: 1367-5931 Impact factor: 8.822