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Phenothiazine-linked nucleosides and nucleotides for redox labelling of DNA

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F17%3A00479760" target="_blank" >RIV/61388963:_____/17:00479760 - isvavai.cz</a>

  • Alternative codes found

    RIV/68081707:_____/17:00479760 RIV/00216224:14740/17:00095595 RIV/00216208:11310/17:10367339

  • Result on the web

    <a href="http://pubs.rsc.org/en/content/articlehtml/2017/ob/c7ob01439b" target="_blank" >http://pubs.rsc.org/en/content/articlehtml/2017/ob/c7ob01439b</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c7ob01439b" target="_blank" >10.1039/c7ob01439b</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Phenothiazine-linked nucleosides and nucleotides for redox labelling of DNA

  • Original language description

    Nucleosides and 2'-deoxyribonucleoside triphosphates (dNTPs) bearing phenothiazine (PT) attached to a nucleobase (cytosine or 7-deazaadenine) either directly or through an acetylene linker were prepared through Suzuki or Sonogashira cross-coupling and triphosphorylation, and were studied as building blocks for polymerase construction of modified DNA. The directly PT-substituted dNTPs were better substrates for polymerases than the alkyne-linked dNTPs but all of them were used in enzymatic synthesis of DNA using primer extension, nicking enzyme amplification, PCR or 3'-tail labelling by terminal deoxynucleotidyl transferase. The phenothiazine served as an oxidizable redox label (giving two analytically useful signals of oxidation on electrode) for nucleosides and DNA and was also used in orthogonal combination with previously developed benzofurazane or nitrophenyl labels for redox coding of DNA bases. Therefore, the title PT-linked dNTPs are useful additions to the portfolio of nucleotides for enzymatic synthesis of redox-labelled DNA for electrochemical analysis.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10401 - Organic chemistry

Result continuities

  • Project

    <a href="/en/project/GBP206%2F12%2FG151" target="_blank" >GBP206/12/G151: Center of novel approaches to bioanalysis and molecular diagnostics</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Organic & Biomolecular Chemistry

  • ISSN

    1477-0520

  • e-ISSN

  • Volume of the periodical

    15

  • Issue of the periodical within the volume

    33

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    13

  • Pages from-to

    6984-6996

  • UT code for WoS article

    000411448200017

  • EID of the result in the Scopus database

    2-s2.0-85028298656