Literature DB >> 16438051

Synthesis of a convenient thymidine glycol phosphoramidite monomer and its site-specific incorporation into DNA fragments.

Didier Gasparutto1, Sonia Cognet, Solveig Roussel, Jean Cadet.   

Abstract

An original phosphoramidite building block of the thymidine glycol lesion has been prepared taking into account the additional diol function and the high lability of this oxidatively induced nucleobase damage. Then the modified nucleoside was site-specifically inserted into DNA fragments by solid support assembling followed by a "one-step" mild final deprotection treatment.

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Year:  2005        PMID: 16438051     DOI: 10.1080/15257770500267279

Source DB:  PubMed          Journal:  Nucleosides Nucleotides Nucleic Acids        ISSN: 1525-7770            Impact factor:   1.381


  3 in total

1.  Synthesis and thermodynamic studies of oligodeoxyribonucleotides containing tandem lesions of thymidine glycol and 8-oxo-2'-deoxyguanosine.

Authors:  Yuesong Wang; Yinsheng Wang
Journal:  Chem Res Toxicol       Date:  2006-06       Impact factor: 3.739

Review 2.  Biological properties of single chemical-DNA adducts: a twenty year perspective.

Authors:  James C Delaney; John M Essigmann
Journal:  Chem Res Toxicol       Date:  2007-12-12       Impact factor: 3.739

Review 3.  Radiation-mediated formation of complex damage to DNA: a chemical aspect overview.

Authors:  J-L Ravanat; J Breton; T Douki; D Gasparutto; A Grand; W Rachidi; S Sauvaigo
Journal:  Br J Radiol       Date:  2014-03       Impact factor: 3.039

  3 in total

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