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Interaction of a Potential Anticancer Agent Hypericin and its Model Compound Emodin with DNA and Bovine Serum Albumin

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F18%3A10379667" target="_blank" >RIV/00216208:11110/18:10379667 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.21873/invivo.11347" target="_blank" >https://doi.org/10.21873/invivo.11347</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.21873/invivo.11347" target="_blank" >10.21873/invivo.11347</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Interaction of a Potential Anticancer Agent Hypericin and its Model Compound Emodin with DNA and Bovine Serum Albumin

  • Original language description

    Background/Aim: We report the incorporation of prospective anticancer agent hypericin into DNA and bovine serum albumin (BSA), respectively, with emphasis on comparison of the differences in interaction mode between hypericin and its model compound emodin. Materials and Methods: Spectrophotometric methods were used for determination of the binding constants of the drug complex with biomacromolecules. Differential scanning calorimetry was applied for evaluation of drug-macromolecule complex thermal stability. Results: The strength of interaction expressed by binding constants was found to be 4.0x10(4) l/mol for hypericin-DNA and 8.1x10(4) l/mol for emodin-DNA complex. Both molecules stabilize bovine serum albumin macromolecule and bind into the hydrophobic cavity in IIA subunit but their localization within the molecule is different. Conclusion: Anticancer agent hypericin and its derivative emodin interact with DNA with medium strength and are probably incorporated into the groove of DNA by hydrogen bonds. Bovine serum albumin can serve as a transport protein for hypericin since the binding force between both molecules is adequate.

  • 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

    10610 - Biophysics

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2018

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    In Vivo

  • ISSN

    0258-851X

  • e-ISSN

  • Volume of the periodical

    32

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    GR - GREECE

  • Number of pages

    8

  • Pages from-to

    1063-1070

  • UT code for WoS article

    000442807900010

  • EID of the result in the Scopus database

    2-s2.0-85053040911