Literature DB >> 11553474

Direct measurement of pyrimidine C6-hydrate stability.

K Nolan Carter1, M M Greenberg.   

Abstract

Pyrimidine C6-hydrates are produced via UV-irradiation and undergo dehydration upon standing. The stability of these compounds has a direct bearing on their genotoxicity. The rate constants for elimination from 5'-benzyoylated derivatives of 5,6-dihydro-5-hydroxythymidine (6) and 5,6-dihydro-5-hydroxy-2'-deoxyuridine (9) were measured directly via HPLC. The rate constants for dehydration increase from pH 6.0 to 8.0. The half-lives for 6 and 9 at pH 7.4 and 37 degrees C are 46.5 and 24.4h, respectively. Deglycosylation is not observed, even upon heating at 90 degrees C. These observations reinforce proposals that pyrimidine hydrates are sufficiently long-lived that they can exert significant effects on biological systems.

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Year:  2001        PMID: 11553474     DOI: 10.1016/s0968-0896(01)00137-7

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  3 in total

1.  DNA tandem lesion repair by strand displacement synthesis and nucleotide excision repair.

Authors:  Shuhei Imoto; Leslie A Bransfield; Deborah L Croteau; Bennett Van Houten; Marc M Greenberg
Journal:  Biochemistry       Date:  2008-03-15       Impact factor: 3.162

2.  Photochemical generation and reactivity of the 5,6-dihydrouridin-6-yl radical.

Authors:  Cory A Newman; Marino J E Resendiz; Jonathan T Sczepanski; Marc M Greenberg
Journal:  J Org Chem       Date:  2009-09-18       Impact factor: 4.354

3.  The mutagenicity of thymidine glycol in Escherichia coli is increased when it is part of a tandem lesion.

Authors:  Haidong Huang; Shuhei Imoto; Marc M Greenberg
Journal:  Biochemistry       Date:  2009-08-25       Impact factor: 3.162

  3 in total

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