| Literature DB >> 28590540 |
Abstract
Bicyclic peptides have greater conformational rigidity and metabolic stability than linear and monocyclic peptides and are capable of binding to challenging drug targets with antibody-like affinity and specificity. Powerful combinatorial library technologies have recently been developed to rapidly synthesize and screen large bicyclic peptide libraries for ligands against enzymes, receptors, and protein-protein interaction targets. Bicyclic peptides have been developed as potential therapeutics against a wide range of diseases, drug targeting agents, imaging/diagnostic probes, and research tools. In this Minireview, we provide a summary of the recent progresses on the synthesis and applications of bicyclic peptides.Entities:
Keywords: click chemistry; combinatorial chemistry; peptides; phage display; protein-protein interactions
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Year: 2017 PMID: 28590540 PMCID: PMC5603421 DOI: 10.1002/chem.201702117
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236