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Cu(I) and Cu(II) Complexes Based on Lonidamine-Conjugated Ligands Designed to Promote Synergistic Antitumor Effects

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F22%3A10457101" target="_blank" >RIV/00216208:11320/22:10457101 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=r9nXxV76Pl" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=r9nXxV76Pl</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acs.inorgchem.1c03658" target="_blank" >10.1021/acs.inorgchem.1c03658</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Cu(I) and Cu(II) Complexes Based on Lonidamine-Conjugated Ligands Designed to Promote Synergistic Antitumor Effects

  • Original language description

    Bis(pyrazol-1-yl)- and bis(3,5-dimethylpyrazol-1-yl)-acetates were conjugated with the 2-hydroxyethylester and 2-aminoethylamide derivatives of the antineoplastic drug lonidamine to prepare Cu(I) and Cu(II) complexes that mightact through synergistic mechanisms of action due to the presence of lonidamine and copper in the same chemical entity. Synchrotron radiation-based complementarytechniques [X-ray photorlectron spectroscopy and near-edge X-ray absorptionfinestructure (NEXAFS)] were used to characterize the electronic and molecularstructures of the complexes and the local structure around the copper ion (XAFS) inselected complexes. All complexes showed significant antitumor activity, proving tobe more effective than the reference drug cisplatin in a panel of human tumor celllines, and were able to overcome oxaliplatin and multidrug resistance. Noticeably,these Cu complexes appeared much more effective than cisplatin against 3Dspheroids of pancreatic PSN-1 cancer cells; among these, PPh3-containing Cu(I)complex15appeared to be the most promising derivative. Mechanistic studies revealed that15induced cancer cell death by means of an apoptosis-alternative cell death

  • 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

    10305 - Fluids and plasma physics (including surface physics)

Result continuities

  • Project

  • Continuities

Others

  • Publication year

    2022

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Inorganic Chemistry

  • ISSN

    0020-1669

  • e-ISSN

    1520-510X

  • Volume of the periodical

    61

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    19

  • Pages from-to

    4919-4937

  • UT code for WoS article

    000779822100013

  • EID of the result in the Scopus database

    2-s2.0-85127248616