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- W4223971737 abstract "Proteins are polymeric compounds formed from amino acids and they exhibit a number of biopotent interactions with other proteins, peptides, nucleotides and other molecules in living cells. The development of non-natural or structurally modified peptides and proteins as peptidomimetics have emerged as promising therapeutic filed to regulate dysfunctioning of protein–protein interactions (PPI)-mediated processes in biological systems. The cyclic peptidomimetics are helpful to modulate PPIs thus are potent for the treatment of autoimmunity, neurodegenerative disorders, infections, cancer, and many other human diseases. This chapter presents some of the latest and noteworthy developments for the preparation of cyclic peptidomimetics. Enzyme-mediated cyclization strategies have become promising choice for chemical-free preparation of cyclic peptidomimetics. A number of enzymes including macrocyclase, thioesterase, sortase and butelase are well-known for ring closure of peptides. The chapter demonstrates the accessibility of single conformers of featured compounds through solid-phase synthetic strategy." @default.
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- W4223971737 date "2022-04-15" @default.
- W4223971737 modified "2023-10-12" @default.
- W4223971737 title "Recent Advances in the Design and Synthesis of Cyclic Peptidomimetics" @default.
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- W4223971737 doi "https://doi.org/10.1002/9781119757153.ch21" @default.
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