Cu(I) and Cu(II) Complexes Based on Lonidamine-Conjugated Ligands Designed to Promote Synergistic Antitumor Effects
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F22%3A10457101" target="_blank" >RIV/00216208:11320/22:10457101 - isvavai.cz</a>
Result on the web
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=r9nXxV76Pl" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=r9nXxV76Pl</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acs.inorgchem.1c03658" target="_blank" >10.1021/acs.inorgchem.1c03658</a>
Alternative languages
Result language
angličtina
Original language name
Cu(I) and Cu(II) Complexes Based on Lonidamine-Conjugated Ligands Designed to Promote Synergistic Antitumor Effects
Original language description
Bis(pyrazol-1-yl)- and bis(3,5-dimethylpyrazol-1-yl)-acetates were conjugated with the 2-hydroxyethylester and 2-aminoethylamide derivatives of the antineoplastic drug lonidamine to prepare Cu(I) and Cu(II) complexes that mightact through synergistic mechanisms of action due to the presence of lonidamine and copper in the same chemical entity. Synchrotron radiation-based complementarytechniques [X-ray photorlectron spectroscopy and near-edge X-ray absorptionfinestructure (NEXAFS)] were used to characterize the electronic and molecularstructures of the complexes and the local structure around the copper ion (XAFS) inselected complexes. All complexes showed significant antitumor activity, proving tobe more effective than the reference drug cisplatin in a panel of human tumor celllines, and were able to overcome oxaliplatin and multidrug resistance. Noticeably,these Cu complexes appeared much more effective than cisplatin against 3Dspheroids of pancreatic PSN-1 cancer cells; among these, PPh3-containing Cu(I)complex15appeared to be the most promising derivative. Mechanistic studies revealed that15induced cancer cell death by means of an apoptosis-alternative cell death
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10305 - Fluids and plasma physics (including surface physics)
Result continuities
Project
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Continuities
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Others
Publication year
2022
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
61
Issue of the periodical within the volume
12
Country of publishing house
US - UNITED STATES
Number of pages
19
Pages from-to
4919-4937
UT code for WoS article
000779822100013
EID of the result in the Scopus database
2-s2.0-85127248616