Podrobno

Structure and solution biospeciation on tricarbonylrhenium(I) complexes of mercaptopyrimidines with multifaceted biological activity
ID Rapuš, Uroš (Avtor), ID Pivarcsik, Tamás (Avtor), ID Dömötör, Orsolya (Avtor), ID Nové, Márta (Avtor), ID Nyári, József (Avtor), ID Bogdanov, Anita (Avtor), ID Spengler, Gabriella (Avtor), ID Turel, Iztok (Avtor), ID Kljun, Jakob (Avtor), ID Enyedy, Éva Anna (Avtor)

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Izvleček
In this study, we report the synthesis and detailed characterization of four novel bidentate (N, N) ligands incorporating a 2-(methylthio)pyrimidine moiety and their fac-tricarbonylrhenium(I) complexes (ReB1–ReB4 and ReB1Aq) with the general formula fac-[Re(CO)$_3$(N,N)X]$^{n+}$, with X = Cl$^−$ or H$_2$O and n = 0 or 1. Designed to integrate biologically relevant functionalities, these complexes exhibited promising multifunctional bioactivity. Cytotoxicity assays demonstrated moderate activity (IC$_{50}$ = 11–78 µM) on various human cancer cell lines, with certain derivatives showing notable selectivity toward the Colo205 line. Most of the chlorido complexes effectively inhibited the replication of Herpes simplex virus type 2, while ReB4 displayed significant antibacterial activity against Staphylococcus aureus, including methicillin-resistant strains (MIC = 12.5–25 µM), and demonstrated biofilm inhibition. Aqueous stability of these organometallic complexes was thoroughly investigated, and complexes ReB2 and ReB3 containing a pyrimidine and a thiazole ring, respectively, gradually decompose in aqueous media, correlating with a decline in anticancer activity. Ligand-exchange processes were observed, in which the chlorido co-ligands were replaced by water, thus affecting the solubility and lipophilicity. The aqua complex ReB1Aq exhibited a low chloride affinity, and the pK$_a$ of the coordinated water molecule was obtained to be ∼8. Its interaction with human serum albumin was investigated in detail and was found to be dominated by non-covalent interactions, indicating that no coordination bond formation occurs with the protein.

Jezik:Angleški jezik
Ključne besede:rhenium, rhenium(I) complexes, mercaptopyrimidines
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:FKKT - Fakulteta za kemijo in kemijsko tehnologijo
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2026
Št. strani:17 str.
Številčenje:Vol. 18, iss. 1, art. mfag002
PID:20.500.12556/RUL-179684 Povezava se odpre v novem oknu
UDK:546.719:547.85
ISSN pri članku:1756-5901
DOI:10.1093/mtomcs/mfag002 Povezava se odpre v novem oknu
COBISS.SI-ID:268827651 Povezava se odpre v novem oknu
Datum objave v RUL:20.02.2026
Število ogledov:198
Število prenosov:49
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Metallomics
Skrajšan naslov:Metallomics
Založnik:Royal Society of Chemistry
ISSN:1756-5901
COBISS.SI-ID:515105049 Povezava se odpre v novem oknu

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:renij, renijevi(I) kompleksi, merkaptopirimidini

Projekti

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P1-0175-2018
Naslov:Napredna anorganska kemija

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:I0-0022-2022
Naslov:Mreža raziskovalnih infrastrukturnih centrov Univerze v Ljubljani (MRIC UL)

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