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Novel cytotoxic 1,10-phenanthroline-triterpenoid amphiphiles with supramolecular characteristics capable of coordinating Cu-64(ii) labels

  1. 1.
    SYSNO ASEP0563219
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleNovel cytotoxic 1,10-phenanthroline-triterpenoid amphiphiles with supramolecular characteristics capable of coordinating Cu-64(ii) labels
    Author(s) Bildziukevich, Uladzimir (UEB-Q) RID, ORCID
    Özdemir, Zülal (UEB-Q) ORCID
    Šaman, David (UOCHB-X) RID, ORCID
    Vlk, M. (CZ)
    Šlouf, Miroslav (UMCH-V) RID, ORCID
    Rárová, L. (CZ)
    Wimmer, Zdeněk (UEB-Q) RID, ORCID
    Number of authors7
    Source TitleOrganic & Biomolecular Chemistry. - : Royal Society of Chemistry - ISSN 1477-0520
    Roč. 20, č. 41 (2022), s. 8157-8163
    Number of pages7 s.
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsBETULINIC ACID ; CHELATORS ; SQUALAMINE
    OECD categoryOrganic chemistry
    R&D ProjectsFV10599 GA MPO - Ministry of Industry and Trade (MPO)
    TN01000008 GA TA ČR - Technology Agency of the Czech Republic (TA ČR)
    Method of publishingLimited access
    Institutional supportUEB-Q - RVO:61389030 ; UOCHB-X - RVO:61388963 ; UMCH-V - RVO:61389013
    UT WOS000865941400001
    EID SCOPUS85140856013
    DOI10.1039/d2ob01172g
    Annotation1,10-Phenanthroline was decorated with triterpenoid-based substituents bearing additional spermine units to form amphiphilic molecules. The synthetic procedure designed for the new phenanthroline-triterpenoid amphiphiles is described in detail. Besides 1,10-phenanthroline, all target structures bear 1,4-disubstituted 1,2,3-triazole rings. The target compounds self-assembled into either helical-like or sheet-like nanostructures, depending on the structure of the target molecule, either based on betulinic acid or oleanolic acid, and on the way of binding spermine subunits to the rest of the molecules. They also proved their ability to coordinate Cu-64(ii) ions. Finally, the target compounds showed cytotoxicity that was partly dependent on the formation of nanostructures.
    WorkplaceInstitute of Experimental Botany
    ContactDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Year of Publishing2023
    Electronic addresshttps://doi.org/10.1039/d2ob01172g
Number of the records: 1  

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