| Literature DB >> 27856346 |
Nir Qvit1, Samuel J S Rubin2, Travis J Urban3, Daria Mochly-Rosen4, Eric R Gross5.
Abstract
Natural endogenously occurring peptides exhibit desirable medicinal properties, but are often limited in application by rapid proteolysis and inadequate membrane permeability. However, editing naturally occurring peptide sequences to develop peptidomimetic analogs created a promising class of therapeutics that can augment or inhibit molecular interactions. Here, we discuss a variety of chemical modifications, including l to d isomerization, cyclization, and unnatural amino acid substitution, as well as design strategies, such as attachment to cell-penetrating peptides, which are used to develop peptidomimetics. We also provide examples of approved peptidomimetics and discuss several compounds in clinical trials.Entities:
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Year: 2016 PMID: 27856346 PMCID: PMC5759319 DOI: 10.1016/j.drudis.2016.11.003
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851