Detailed Information on Publication Record
2020
The first copper(II) complex with 1,10-phenanthroline and salubrinal with interesting biochemical properties.
MASURI, Sebastiano, Enzo CADONI, Maria Grazia CABIDDU, Francesco ISAIA, Maria Giovanna DEMURU et. al.Basic information
Original name
The first copper(II) complex with 1,10-phenanthroline and salubrinal with interesting biochemical properties.
Authors
MASURI, Sebastiano (380 Italy), Enzo CADONI (380 Italy), Maria Grazia CABIDDU (380 Italy), Francesco ISAIA (380 Italy), Maria Giovanna DEMURU (380 Italy), Lukáš MORÁŇ (203 Czech Republic, belonging to the institution), David BUČEK (203 Czech Republic), Petr VAŇHARA (203 Czech Republic, belonging to the institution), Josef HAVEL (203 Czech Republic, belonging to the institution) and Tiziana PIVETTA (380 Italy, guarantor)
Edition
Metallomics, Cambridge, Royal Society of Chemistry, 2020, 1756-5901
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10600 1.6 Biological sciences
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 4.526
RIV identification code
RIV/00216224:14110/20:00116696
Organization unit
Faculty of Medicine
UT WoS
000542894500004
Keywords in English
Unfolded Protein Response; X Box Binding Protein 1; Activating Transcription Factor 6
Tags
International impact, Reviewed
Změněno: 27/1/2021 10:09, Mgr. Tereza Miškechová
Abstract
V originále
The novel copper complex [Cu(phen)(2)(salubrinal)](ClO4)(2)(C0SAL) has been synthesised and characterised. Copper(ii) is coordinated by salubrinal through the thionic group, as shown by the UV-Vis, IR, ESI-MS and tandem mass results, together with the theoretical calculations. The formed complex showed a DPPH radical scavenging ability higher than that of salubrinal alone. Studies on lipid oxidation inhibition showed that theC0SALconcentration, required to inhibit the enzyme, was lower than that of salubrinal. The inhibition of the enzyme could take placeviaallosteric modulation, as suggested by docking calculations.C0SALshowed a good cytotoxic activity on A2780 cells, 82 fold higher than that of the precursor salubrinal and 1.4 fold higher than that of [Cu(phen)(2)(H2O)](ClO4)(2). Treatment withC0SALin SKOV3 ovarian cancer cells induced expression of GRP-78 and DDIT3 regulators of ER-stress response. The cytotoxic effect ofC0SALwas reverted in the presence of TUDCA, suggesting thatC0SALinduces cell death through ER-stress. In A2780 cells treated withC0SAL gamma-H2AX was accumulated, suggesting that DNA damage was also involved.
Links
LM2018129, research and development project |
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