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Pregled bibliografske jedinice broj: 1135453

Copper(II) Salicylideneimine Complexes Revisited: From a Novel Derivative and Extended Characterization of Two Homologues to Interaction with BSA and Antiproliferative Activity


Memišević, Mahira; Zahirović, Adnan; Višnjevac, Aleksandar; Osmanović, Amar; Žilić, Dijana; Kralj, Marijeta; Muratović, Senada; Martin-Kleiner, Irena; Završnik, Davorka; Kahrović, Emira
Copper(II) Salicylideneimine Complexes Revisited: From a Novel Derivative and Extended Characterization of Two Homologues to Interaction with BSA and Antiproliferative Activity // Inorganica chimica acta, 525 (2021), 120460, 9 doi:10.1016/j.ica.2021.120460 (međunarodna recenzija, članak, znanstveni)


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Naslov
Copper(II) Salicylideneimine Complexes Revisited: From a Novel Derivative and Extended Characterization of Two Homologues to Interaction with BSA and Antiproliferative Activity

Autori
Memišević, Mahira ; Zahirović, Adnan ; Višnjevac, Aleksandar ; Osmanović, Amar ; Žilić, Dijana ; Kralj, Marijeta ; Muratović, Senada ; Martin-Kleiner, Irena ; Završnik, Davorka ; Kahrović, Emira

Izvornik
Inorganica chimica acta (0020-1693) 525 (2021); 120460, 9

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Antiproliferative activity ; BSA ; Copper(II) Schiff bases ; Docking study ; N-alkylsalicyiladimines

Sažetak
A novel compound bis[N-n-propyl-5-chloro-2-oxy-κO- benzylideneimine-κN-(1–)]copper(II) was prepared, along with two previously reported homologues having N-n-propylsalicylideneimine and N-n-buthyl- 5-chlorosalicylideneimine ligands. Single crystal X-ray determination of three complexes reveals almost ideal CuO2N2 trans-square planar geometry. All three compounds crystalize in P-1 space group. Infrared spectra confirm coordination of iminophenolate via azomethine nitrogen and deprotonated phenolic oxygen. Electronic spectra showed strong iminophenolate-to-Cu(II) charge transfer transitions in the region 359–371 nm and d-d transition centered around 600 nm. The location of an unpaired electron of d9 configuration Cu(II), in dx2−y2 orbital is confirmed based on g-tensor values obtained by X- band ESR spectroscopy that also corresponds to square planar geometry. Cyclic voltammograms in acetonitrile solution showed one-electron reduction with cathodic peaks in the range –0.598 to –0.618 V as a result of the fast decomplexation and disproportionation of the Cu(I) complex. The interaction with BSA (Bovine serum albumin) showed 1:1 complex-protein binding with Kb constants values in 103 –105 M−1 range. Docking calculations point out only hydrophobic and π-π interactions between copper(II) complexes and BSA with average distances between two tryptophan residues and copper complexes in 20–24 Å range. Antiproliferative testing on two tumor cell lines H460 and HCT116 and non-tumor HEK293T showed non- selectivity and close IC50 values for tumor and control lines.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Ustanove:
Institut "Ruđer Bošković", Zagreb

Poveznice na cjeloviti tekst rada:

doi www.sciencedirect.com doi.org

Citiraj ovu publikaciju:

Memišević, Mahira; Zahirović, Adnan; Višnjevac, Aleksandar; Osmanović, Amar; Žilić, Dijana; Kralj, Marijeta; Muratović, Senada; Martin-Kleiner, Irena; Završnik, Davorka; Kahrović, Emira
Copper(II) Salicylideneimine Complexes Revisited: From a Novel Derivative and Extended Characterization of Two Homologues to Interaction with BSA and Antiproliferative Activity // Inorganica chimica acta, 525 (2021), 120460, 9 doi:10.1016/j.ica.2021.120460 (međunarodna recenzija, članak, znanstveni)
Memišević, M., Zahirović, A., Višnjevac, A., Osmanović, A., Žilić, D., Kralj, M., Muratović, S., Martin-Kleiner, I., Završnik, D. & Kahrović, E. (2021) Copper(II) Salicylideneimine Complexes Revisited: From a Novel Derivative and Extended Characterization of Two Homologues to Interaction with BSA and Antiproliferative Activity. Inorganica chimica acta, 525, 120460, 9 doi:10.1016/j.ica.2021.120460.
@article{article, author = {Memi\v{s}evi\'{c}, Mahira and Zahirovi\'{c}, Adnan and Vi\v{s}njevac, Aleksandar and Osmanovi\'{c}, Amar and \v{Z}ili\'{c}, Dijana and Kralj, Marijeta and Muratovi\'{c}, Senada and Martin-Kleiner, Irena and Zavr\v{s}nik, Davorka and Kahrovi\'{c}, Emira}, year = {2021}, pages = {9}, DOI = {10.1016/j.ica.2021.120460}, chapter = {120460}, keywords = {Antiproliferative activity, BSA, Copper(II) Schiff bases, Docking study, N-alkylsalicyiladimines}, journal = {Inorganica chimica acta}, doi = {10.1016/j.ica.2021.120460}, volume = {525}, issn = {0020-1693}, title = {Copper(II) Salicylideneimine Complexes Revisited: From a Novel Derivative and Extended Characterization of Two Homologues to Interaction with BSA and Antiproliferative Activity}, keyword = {Antiproliferative activity, BSA, Copper(II) Schiff bases, Docking study, N-alkylsalicyiladimines}, chapternumber = {120460} }
@article{article, author = {Memi\v{s}evi\'{c}, Mahira and Zahirovi\'{c}, Adnan and Vi\v{s}njevac, Aleksandar and Osmanovi\'{c}, Amar and \v{Z}ili\'{c}, Dijana and Kralj, Marijeta and Muratovi\'{c}, Senada and Martin-Kleiner, Irena and Zavr\v{s}nik, Davorka and Kahrovi\'{c}, Emira}, year = {2021}, pages = {9}, DOI = {10.1016/j.ica.2021.120460}, chapter = {120460}, keywords = {Antiproliferative activity, BSA, Copper(II) Schiff bases, Docking study, N-alkylsalicyiladimines}, journal = {Inorganica chimica acta}, doi = {10.1016/j.ica.2021.120460}, volume = {525}, issn = {0020-1693}, title = {Copper(II) Salicylideneimine Complexes Revisited: From a Novel Derivative and Extended Characterization of Two Homologues to Interaction with BSA and Antiproliferative Activity}, keyword = {Antiproliferative activity, BSA, Copper(II) Schiff bases, Docking study, N-alkylsalicyiladimines}, chapternumber = {120460} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


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