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- W4386836633 endingPage "106860" @default.
- W4386836633 startingPage "106860" @default.
- W4386836633 abstract "Nucleic acid represents the ideal drug candidate for protein targets that are hard to target or against which drug development is not easy. Peptide nucleic acids (PNAs) are synthesized by attaching modified peptide backbones generally derived from repetitive N-2-aminoethyl glycine units in place of the regular phosphodiester backbone and represent synthetic impersonator of nucleic acids that offers an exciting research field due to their fascinating spectrum of biotechnological, diagnostic and potential therapeutic applications. The semi-rigid peptide nucleic acid backbone serves as a nearly-perfect template for attaching complimentary base pairs on DNA or RNA in a sequence-dependent manner as described by Watson-Crick models. PNAs and their analogues are endowed with exceptionally high affinity and specificity for receptor sites, essentially due to their polyamide backbone's uncharged and flexible nature. The present review compiled various strategies to modify the polypeptide backbone for improving the target selectivity and stability of the PNAs in the body. The investigated biological activities carried out on PNAs have also been summarized in the present review." @default.
- W4386836633 created "2023-09-19" @default.
- W4386836633 creator A5042250425 @default.
- W4386836633 creator A5082736233 @default.
- W4386836633 date "2023-12-01" @default.
- W4386836633 modified "2023-09-27" @default.
- W4386836633 title "Peptide Nucleic Acids: Recent Developments in the Synthesis and Backbone Modifications" @default.
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