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Platinum(IV) and platinum(II) anticancer complexes with biologically active releasable ligands

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F24%3A73627676" target="_blank" >RIV/61989592:15310/24:73627676 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://www.sciencedirect.com/science/article/pii/S0010854523005672" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0010854523005672</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.ccr.2023.215578" target="_blank" >10.1016/j.ccr.2023.215578</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Platinum(IV) and platinum(II) anticancer complexes with biologically active releasable ligands

  • Popis výsledku v původním jazyce

    The concept of multi-action octahedral platinum(IV) complexes is based on the rational derivatization of anticancer square-planar platinum(II) compounds (e.g., cisplatin or oxaliplatin) by a bioactive axial ligand(s) bearing its own biological effect. Over the years, many multi-action Pt(IV) complexes have been reported to exhibit an extraordinarily high anticancer effect both in vitro and in vivo, and, importantly, to kill cancer cells through a unique mechanism of action (MoA), combining effects of parent Pt(II) species and released bioactive ligand(s). In this review article, we summarized the structural types of Pt(IV) complexes reported to date in the literature, and these complexes were categorized according to various criteria - the parent Pt(II) complex, the number and type of bioactive ligands, type of the second (either bioactive or innocent) axial ligand, and nuclearity (homometallic and heterometallic Pt(IV) complexes are involved). Most of the multi-action Pt(IV) complexes reported so far include carboxylates as axial ligands, and they are classified among bis(carboxylato) complexes, mono(carboxylato) complexes with hydroxide/chloride or a different group as the other axial ligand. A smaller group is represented by non-carboxylato complexes, which involve carbonato, carbamato or thiocarbonato groups as well releasing bioactive Pt(II) species and bioactive ligand(s) as well, which allowed also a critical comparison of the paid to the discussion of solution behaviour, activation towards the release of a bioactive ligand(s) and biological activity of the reviewed types of Pt complexes. A relevant comparison of these crucial features of multi-action Pt complexes is beneficial for future development of these pharmacologically highly prospective compounds.

  • Název v anglickém jazyce

    Platinum(IV) and platinum(II) anticancer complexes with biologically active releasable ligands

  • Popis výsledku anglicky

    The concept of multi-action octahedral platinum(IV) complexes is based on the rational derivatization of anticancer square-planar platinum(II) compounds (e.g., cisplatin or oxaliplatin) by a bioactive axial ligand(s) bearing its own biological effect. Over the years, many multi-action Pt(IV) complexes have been reported to exhibit an extraordinarily high anticancer effect both in vitro and in vivo, and, importantly, to kill cancer cells through a unique mechanism of action (MoA), combining effects of parent Pt(II) species and released bioactive ligand(s). In this review article, we summarized the structural types of Pt(IV) complexes reported to date in the literature, and these complexes were categorized according to various criteria - the parent Pt(II) complex, the number and type of bioactive ligands, type of the second (either bioactive or innocent) axial ligand, and nuclearity (homometallic and heterometallic Pt(IV) complexes are involved). Most of the multi-action Pt(IV) complexes reported so far include carboxylates as axial ligands, and they are classified among bis(carboxylato) complexes, mono(carboxylato) complexes with hydroxide/chloride or a different group as the other axial ligand. A smaller group is represented by non-carboxylato complexes, which involve carbonato, carbamato or thiocarbonato groups as well releasing bioactive Pt(II) species and bioactive ligand(s) as well, which allowed also a critical comparison of the paid to the discussion of solution behaviour, activation towards the release of a bioactive ligand(s) and biological activity of the reviewed types of Pt complexes. A relevant comparison of these crucial features of multi-action Pt complexes is beneficial for future development of these pharmacologically highly prospective compounds.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10402 - Inorganic and nuclear chemistry

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2024

  • Kód důvěrnosti údajů

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

Údaje specifické pro druh výsledku

  • Název periodika

    Coordination Chemistry Reviews

  • ISSN

    0010-8545

  • e-ISSN

    1873-3840

  • Svazek periodika

    501

  • Číslo periodika v rámci svazku

    FEB

  • Stát vydavatele periodika

    NL - Nizozemsko

  • Počet stran výsledku

    38

  • Strana od-do

    "215578-1"-"215578-38"

  • Kód UT WoS článku

    001140193400001

  • EID výsledku v databázi Scopus

    2-s2.0-85179612856