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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
)
PDF - Predstavitvena datoteka,
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MD5: B63FB3FB837A6C0941EBD700F1BDBFEF
URL - Izvorni URL, za dostop obiščite
https://academic.oup.com/metallomics/article/18/1/mfag002/8427332
Galerija slik
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
UDK:
546.719:547.85
ISSN pri članku:
1756-5901
DOI:
10.1093/mtomcs/mfag002
COBISS.SI-ID:
268827651
Datum objave v RUL:
20.02.2026
Število ogledov:
198
Število prenosov:
49
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Objavi na:
Gradivo je del revije
Naslov:
Metallomics
Skrajšan naslov:
Metallomics
Založnik:
Royal Society of Chemistry
ISSN:
1756-5901
COBISS.SI-ID:
515105049
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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