52 / 2023-08-14 18:11:01
Chelate metal complexes of dialkylphosphorylpyridines and quinolines and their cytotoxity.
phosphine oxide, pyridine, quinolone, complexes, cytotoxity
Abstract Accepted
Elvira Musina / Arbuzov Institute of Organic and Physical Chemistry; FRC Kazan Scientific Center; Russian Academy of Sciences
Kamila Enikeeva / Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences
Airat Kasimov / Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences
Alexandra Voloshina / Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences
Andrey Karasik / Arbuzov Institute of Organic and Physical Chemistry
The approaches to the synthesis of dialkylphosphorylpyridines and quinolones with cyclic and acylic phosphoryl-group was developed. A wide row of their Сu(II), Zn(II), Mn(II) and Ni(II) chelate complexes was synthesized. All obtained ligands and complexes were tested on the cytotoxic activity towards M-Hela and HuTu80 cancer cells as well towards Chang Liver normal cell line. N-heterocycle-containing phosphine oxides themselves are low toxic against Chang Liver normal as well as M-Hela and HuTu80 cancer cell lines, whereas the chelation with a metal ion selectively enhances the cytotoxicity of ligands against cancer cells. Mn(II), Cu(II), and Zn(II) complexes of diisopropylphosphorylquinoline and 1,3,5-diazaphosphorinane P-pyridyl-P-oxide exhibit the high cytotoxicity towards cancer cells with high selectivity (the selectivity index achieves  the values of 15 and 17) exceeding selectivity of known anticancer drugs tamoxifen, doxorubicin, oligomycin, 5-fluorouracil and sorafenib The approaches to the synthesis of dialkylphosphorylpyridines and quinolones with cyclic and acylic phosphoryl-group was developed. A wide row of their Сu(II), Zn(II), Mn(II) and Ni(II) chelate complexes was synthesized. All obtained ligands and complexes were tested on the cytotoxic activity towards M-Hela and HuTu80 cancer cells as well towards Chang Liver normal cell line. N-heterocycle-containing phosphine oxides themselves are low toxic against Chang Liver normal as well as M-Hela and HuTu80 cancer cell lines, whereas the chelation with a metal ion selectively enhances the cytotoxicity of ligands against cancer cells. Mn(II), Cu(II), and Zn(II) complexes of diisopropylphosphorylquinoline and 1,3,5-diazaphosphorinane P-pyridyl-P-oxide exhibit the high cytotoxicity towards cancer cells with high selectivity (the selectivity index achieves  the values of 15 and 17) exceeding selectivity of known anticancer drugs tamoxifen, doxorubicin, oligomycin, 5-fluorouracil and sorafenib
Important Date
  • Conference Date

    Nov 12

    2023

    to

    Nov 16

    2023

  • Oct 24 2023

    Draft paper submission deadline

  • Nov 16 2023

    Registration deadline

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Ningbo University
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