izpis_h1_title_alt

Copper(II) complexes with mixed heterocycle ligands as promising antibacterial and antitumor species
ID Rostas, Arpad Mihai (Author), ID Badea, Mihaela (Author), ID Ruţǎ, Lavinia L. (Author), ID Farcaşanu, Ileana C. (Author), ID Maxim, Cǎtǎlin (Author), ID Chifiriuc, Mariana Carmen (Author), ID Popa, Marcela (Author), ID Luca, Mirela (Author), ID Čelan Korošin, Nataša (Author), ID Cerc Korošec, Romana (Author), ID Bacalum, Mihaela (Author), ID Raileanu, Mina (Author), ID Olar, Rodica (Author)

.pdfPDF - Presentation file, Download (3,80 MB)
MD5: 3034C4D135A13904ADA720D727A5B7DD
URLURL - Source URL, Visit https://www.mdpi.com/1420-3049/25/17/3777 This link opens in a new window

Abstract
Complexes with mixed ligands [Cu(N-N)$_2$(pmtp)](ClO$_4$)$_2$ ((1) N-N: 2,2′-bipyridine; (2) L: 1,10-phenanthroline and pmpt: 5-phenyl-7-methyl-1,2,4-triazolo[1,5-a]pyrimidine) were synthesized and structurally and biologically characterized. Compound (1) crystallizes into space group Pa and (2) in P-1. Both complexes display an intermediate stereochemistry between the two five-coordinated ones. The biological tests indicated that the two compounds exhibited superoxide scavenging capacity, intercalative DNA properties, and metallonuclease activity. Tests on various cell systems indicated that the two complexes neither interfere with the proliferation of Saccharomyces cerevisiae or BJ healthy skin cells, nor cause hemolysis in the active concentration range. Nevertheless, the compounds showed antibacterial potential, with complex (2) being significantly more active than complex (1) against all tested bacterial strains, both in planktonic and biofilm growth state. Both complexes exhibited a very good activity against B16 melanoma cells, with a higher specificity being displayed by compound (1). Taken together, the results indicate that complexes (1) and (2) have specific biological relevance, with potential for the development of antitumor or antimicrobial drugs.

Language:English
Keywords:copper(II) complex, 1, 2, 4-triazolo[1, 5-a]pyrimidine, cytotoxicity, biofilm, metallonuclease activity, DNA intercalation
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Publication status:Published
Publication version:Version of Record
Year:2020
Number of pages:22 str.
Numbering:Vol. 25, iss. 17, art. 3777
PID:20.500.12556/RUL-134318 This link opens in a new window
UDC:546.56:547.853
ISSN on article:1420-3049
DOI:10.3390/molecules25173777 This link opens in a new window
COBISS.SI-ID:26455043 This link opens in a new window
Publication date in RUL:05.01.2022
Views:883
Downloads:121
Metadata:XML RDF-CHPDL DC-XML DC-RDF
:
Copy citation
Share:Bookmark and Share

Record is a part of a journal

Title:Molecules
Shortened title:Molecules
Publisher:MDPI
ISSN:1420-3049
COBISS.SI-ID:18462981 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:01.09.2020

Secondary language

Language:Slovenian
Keywords:baker, bakrovi kompleksi, 1, 2, 4-triazolo[1, 5-a]pirimidin, citotoksičnost

Projects

Funder:ARRS - Slovenian Research Agency
Project number:P1-0134
Name:Kemija za trajnostni razvoj

Similar documents

Similar works from RUL:
Similar works from other Slovenian collections:

Back