5-carboxamido-5-formamido-2-iminohydantoin

 

Topic mentions per year

Topic mentions per year

2006-2017
02420062017

Papers overview

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2015
2015
Exogenously and endogenously produced reactive oxygen species attack the base and sugar moieties of DNA showing a preference for… (More)
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2015
2015
Oxidation of the guanine heterocycle by two electrons can yield the chiral product 5-carboxamido-5-formamido-2-iminohydantoin… (More)
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2015
2015
Guanine (G) is a target for oxidation by reactive oxygen species in DNA, RNA, and the nucleotide pool. Damage to DNA yields… (More)
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2015
2015
The nucleobase guanine in DNA (dG) and RNA (rG) has the lowest standard reduction potential of the bases, rendering it a major… (More)
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2013
2013
Telomere shortening occurs during oxidative and inflammatory stress with guanine (G) as the major site of damage. In this work, a… (More)
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2013
2013
Reduction potentials and pK(a) values were calculated for intermediates and products along three major pathways for guanine… (More)
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2012
2012
The oxidation of an oligonucleotide containing a single nuclease-resistant phosphodiester link, a stereoisomerically pure… (More)
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2012
2012
The exposure of guanine in the oligonucleotide 5'-d(TCGCT) to one-electron oxidants leads initially to the formation of the… (More)
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2011
2011
Reactive oxygen species attack both base and sugar moieties in DNA with a preference among the bases for reaction at guanine. In… (More)
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2006
2006
The nucleobase guanine was oxidized with dimethyldioxirane (DMDO) to explore the role of epoxidizing agents in oxidative DNA… (More)
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