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Coligand-Dependent Cellular Effects and DNA/BSA Binding of Ruthenium(II) Tris(pyrazolylmethane) Complexes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F25%3A73633167" target="_blank" >RIV/61989592:15310/25:73633167 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15640/25:73633167

  • Result on the web

    <a href="https://pubs.acs.org/doi/10.1021/acs.inorgchem.5c04198?src=getftr&utm_source=clarivate&getft_integrator=clarivate" target="_blank" >https://pubs.acs.org/doi/10.1021/acs.inorgchem.5c04198?src=getftr&utm_source=clarivate&getft_integrator=clarivate</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acs.inorgchem.5c04198" target="_blank" >10.1021/acs.inorgchem.5c04198</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Coligand-Dependent Cellular Effects and DNA/BSA Binding of Ruthenium(II) Tris(pyrazolylmethane) Complexes

  • Original language description

    Monocationic [RuCl(kappa 3-tpm)(L)(PPh3)]Cl (L = PPh3, 1; NCMe, 2; 1,3,5-triaza-7-phosphaadamantane (PTA), 3; phosphinoferrocene, 4; 3-methyl-pyrazole, 5; NH2(CH2)2OH, 6; NH2(CH2)2(4-C6H4OH) (tyramine), 7; cyclohexylamine, 8; NH2CH2CH2NH2, 9; tpm = tris-pyrazolylmethane) and bis-cationic ruthenium complexes [RuCl(kappa 3-tpm)(PPh3)(LL&apos;)][NO3]2 (LL &apos; = ethylenediamine, 10; 1,10-phenanthroline, 11; 2-picolylamine, 12; N-phenyl-1-(2-pyridinyl)methanimine, 13) and [RuCl(kappa 3-tpm)(PPh3)(NCMe)2][NO3]2 (14) were evaluated for their anticancer potential. Complexes 4-9 and 13-14 are novel and were obtained in 72-98% yields from thermal exchange reactions of 1. They were characterized by IR and multinuclear NMR spectroscopy, and the solid-state structures of 4, 5, 6, 7, and 14 were determined by single-crystal X-ray diffraction. Complexes 3-8 and 10-14 were further examined for solubility and stability in aqueous media, and octanol/water partition coefficients. The complexes were assessed for their in vitro cytotoxicity on a panel of six cancer and two normal cell lines. Complex 1 and the ruthenium-ferrocenyl conjugate 4 revealed significant-to-moderate activity against the cancer cells, with IC50 values ranging from 1.8 to 25.2 mu M. Mechanistic studies in A2780 cells included time-dependent cytotoxicity, intracellular ruthenium uptake, cell cycle analysis, autophagy induction, production of ROS (reactive oxygen species), and mitochondrial membrane potential measurements. Moreover, a detailed study was conducted to evaluate DNA and bovine serum albumin (BSA) binding capacity. Overall, the results revealed distinct potential mechanisms of action driven by ligand diversity, specifically mitochondrial uncoupling for 1 and 4, and apoptosis- and necrosis-induced cell death for 13 and 14.

  • 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

    10402 - Inorganic and nuclear chemistry

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • 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

    64

  • Issue of the periodical within the volume

    50

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    19

  • Pages from-to

    "24615–24633"

  • UT code for WoS article

    001632715900001

  • EID of the result in the Scopus database

    2-s2.0-105025198363