Synthesis of a Novel Pyrrolidine-based Peptide Nucleic Acid that Contains Tertiary Amines in the Main Chain and Its Internalization into Cells
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference9 articles.
1. Sequence-Selective Recognition of DNA by Strand Displacement with a Thymine-Substituted Polyamide
2. Novel Peptide Nucleic Acid That Shows High Sequence Specificity and All-or-None-Type Hybridization with the Complementary DNA
3. Synthesis of δ-amino acids with an ether linkage in the main chain and nucleobases on the side chain as monomer units for oxy-peptide nucleic acids
4. Hybridization between Oxy-Peptide Nucleic Acids and DNAs: Dependence of Hybrid Stabilities on the Chain-Lengths, Types of Base Pairs, and the Chain Directions
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1. Perspectives on conformationally constrained peptide nucleic acid (PNA): insights into the structural design, properties and applications;RSC Chemical Biology;2022
2. Chemical Synthesis of Conformationally Constrained PNA Monomers;Chemical Synthesis of Nucleoside Analogues;2013-02-15
3. Peptide Nucleic Acids with a Structurally Biased Backbone. Updated Review and Emerging Challenges;Current Topics in Medicinal Chemistry;2011-06-01
4. Antisense effect of pyrrolidine-based oxy-peptide nucleic acids in Escherichia coli;Bioorganic & Medicinal Chemistry Letters;2011-01
5. Quantification of the orientations of pyrrolidine-based oxypeptide nucleic acid–DNA hybrid duplexes;MedChemComm;2011
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