Design and synthesis of intrinsically cell-penetrating nucleopeptides-Reference-Cited by-同舟云学术

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Design and synthesis of intrinsically cell-penetrating nucleopeptides

Published:2008 Issue:20 Volume:6 Page:3661
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Geotti-Bianchini Piero,Beyrath Julien,Chaloin Olivier,Formaggio Fernando,Bianco Alberto

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2008/OB/B811639C

Reference29 articles.

1. Unconventional nucleotide analogues. VI. Synthesis of Purinyl- and Pyrimidinyl-Peptides

2. Synthetic analogues of polynucleotides—XIII

3. Sequence-Selective Recognition of DNA by Strand Displacement with a Thymine-Substituted Polyamide

4. PNA hybridizes to complementary oligonucleotides obeying the Watson–Crick hydrogen-bonding rules

5. PNA Technology

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1. Histidine–DNA nanoarchitecture as laccase mimetic DNAzymes;Nanoscale;2023

2. Willardiine and Its Synthetic Analogues: Biological Aspects and Implications in Peptide Chemistry of This Nucleobase Amino Acid;Pharmaceuticals;2022-10-10

3. Tailoring the Structure of Cell Penetrating DNA and RNA Binding Nucleopeptides;International Journal of Molecular Sciences;2022-07-31

4. Novel insights on nucleopeptide binding: A spectroscopic and in silico investigation on the interaction of a thymine-bearing tetrapeptide with a homoadenine DNA;Journal of Molecular Liquids;2022-02

5. Evidence of Protein Binding by a Nucleopeptide Based on a Thyminedecorated L-Diaminopropanoic Acid through CD and In Silico Studies;Current Medicinal Chemistry;2021-08-13

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