Literature DB >> 25083514

A lipophilic "fully-anti" dodecamer from a (5'S)-5',8-cyclo-2'-deoxyguanosine.

Silvia Pieraccini1, Michael A Terzidis, Enrico J Baldassarri, Giovanna Fragneto, Paolo Mariani, Stefano Masiero, Chryssostomos Chatgilialoglu.   

Abstract

The self-assembly of a lipophilic derivative of (5'S)-5',8-cyclo-2'-deoxyguanosine, a mutagenic product formed by hydroxyl radical attack against DNA, has been investigated. This derivative forms, with high fidelity, a dodecameric complex composed of three stacked G-quartets in the presence of strontium picrate. This is the first example of a fully-anti lipophilic G-quadruplex.

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Year:  2014        PMID: 25083514     DOI: 10.1039/c4cc04275a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

1.  The association constant of 5',8-cyclo-2'-deoxyguanosine with cytidine.

Authors:  Amedeo Capobianco; Tonino Caruso; Sandra Fusco; Michael A Terzidis; Annalisa Masi; Chryssostomos Chatgilialoglu; Andrea Peluso
Journal:  Front Chem       Date:  2015-03-27       Impact factor: 5.221

  1 in total

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