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2'-deoxyaristeromycin

Known as: Cyclopentanemethanol, 4-(6-amino-9H-purin-9-yl)-2-hydroxy-, (1R-(1alpha,2beta,4alpha))- 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

Deoxyadenosines

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2002
2002
The Conformational Study of Two Carbocyclic Nucleosides: Why Carbocyclic Nucleic Acids (CarNAs) Form More Stable Duplexes with RNA than DNA Does
Abstract Replacement of the furanose moiety of DNA with a cyclopentene ring produces a modified sugar analogue: Carbocyclic… Expand
2001
2001
The First Example of a Hoogsteen Basepaired DNA Duplex in Dynamic Equilibrium with a Watson-Crick Basepaired Duplex—A Structural (NMR), Kinetic and Thermodynamic Study
Abstract A single-point substitution of the O4′ oxygen by a CH2 group at the sugar residue of A 6 (i.e. 2′-deoxyaristeromycin… Expand
2000
2000
Structure of an 11-mer DNA Duplex Containing the Carbocyclic Nucleotide Analog: 2′-Deoxyaristeromycin
Abstract 2′-deoxyaristeromycin (dAr) is a nucleoside analogue that is resistant to the action of DNA glycosylases. High… Expand
1999
1999
A single carbocyclic nucleotide substitution in a 12mer DNA gives a Hoogsteen basepaired duplex (till 38 degrees C) and a hairpin (till 65 degrees C). A 600 MHz NMR spectroscopic study.
The impact of intramolecular stereoelectronic effects has been examined by comparison of the solution structures of natural oligo… Expand
1998
1998
Synthesis of enzymatically noncleavable carbocyclic nucleosides for DNA-N-glycosylase studies.
Carbocyclic nucleosides have been of great interest as antiviral agents and in studies in the area of antisense technology. The… Expand
1985
1985
Protected 2'-deoxyaristeromycin on polymer support: a substitute for the acid labile 2'-deoxyadenosine moiety at the 3'-terminus of oligodeoxynucleotides.
A modified nucleoside antibiotic on polymer support was employed in the solid-phase synthesis of two oligodeoxynucleotides to… Expand
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