A cytosine analogue containing a conformationally flexible acyclic linker for triplex formation at sites with contiguous G-C base pairs
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference29 articles.
1. Triplex formation of oligonucleotides containing 2'-O-methylpseudoisocytidine in substitution for 2'-deoxycytidine
2. Use of a pyrimidine nucleoside that functions as a bidentate hydrogen bond donor for the recognition of isolated or contiguous G-C base pairs by oligonucleotide-directed triplex formation
3. A New Pyrimidine Nucleoside (m5oxC) for the pH-Independent Recognition of G-C Base Pairs by Oligonucleotide-Directed Triplex Formation
4. Triplex formation of an oligonucleotide containing 2'-O-methylpseudoisocytidine with a DNA duplex at neutral pH
5. Design of a nonnatural deoxyribonucleoside for recognition of GC base pairs by oligonucleotide-directed triple helix formation
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1. Structure and Stabilization of CGC+Triplex DNA;DNA in Supramolecular Chemistry and Nanotechnology;2017-06-21
2. The Therapeutic Potential of Migrastatin-Core Analogs for the Treatment of Metastatic Cancer;Molecules;2017-02-09
3. Alternative DNA Structures, Switches and Nanomachines;DNA in Supramolecular Chemistry and Nanotechnology;2015-07-23
4. ChemInform Abstract: A Cytosine Analogue Containing a Conformationally Flexible Acyclic Linker for Triplex Formation at Sites with Contiguous G-C Base Pairs.;ChemInform;2010-06-22
5. Rational Design of Functional DNA with a Non-Ribose Acyclic Scaffold;Current Organic Chemistry;2009-07-01
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