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Chelating mitochondrial iron and copper: Recipes, pitfalls and promise

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F24%3A43927060" target="_blank" >RIV/00216208:11120/24:43927060 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1016/j.mito.2024.101903" target="_blank" >https://doi.org/10.1016/j.mito.2024.101903</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.mito.2024.101903" target="_blank" >10.1016/j.mito.2024.101903</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Chelating mitochondrial iron and copper: Recipes, pitfalls and promise

  • Original language description

    Iron and copper chelation therapy plays a crucial role in treating conditions associated with metal overload, such as hemochromatosis or Wilson&apos;s disease. However, conventional chelators face challenges in reaching the core of iron and copper metabolism - the mitochondria. Mitochondria-targeted chelators can specifically target and remove metal ions from mitochondria, showing promise in treating diseases linked to mitochondrial dysfunction, including neurodegenerative diseases and cancer. Additionally, they serve as specific mitochondrial metal sensors. However, designing these new molecules presents its own set of challenges. Depending on the chelator&apos;s intended use to prevent or to promote redox cycling of the metals, the chelating moiety must possess different donor atoms and an optimal value of the electrode potential of the chelator-metal complex. Various targeting moieties can be employed for selective delivery into the mitochondria. This review also provides an overview of the current progress in the design of mitochondria-targeted chelators and their biological activity investigation.

  • 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

    30107 - Medicinal chemistry

Result continuities

  • Project

    <a href="/en/project/LX22NPO5104" target="_blank" >LX22NPO5104: National Institute for Research of Metabolic and Cardiovascular Diseases</a><br>

  • Continuities

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

Others

  • Publication year

    2024

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Mitochondrion

  • ISSN

    1567-7249

  • e-ISSN

    1872-8278

  • Volume of the periodical

    78

  • Issue of the periodical within the volume

    September

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    10

  • Pages from-to

    101903

  • UT code for WoS article

    001247972200001

  • EID of the result in the Scopus database

    2-s2.0-85194348778