Replacement of the phosphodiester backbone between canonical nucleosides with a dirhenium carbonyl "click" linker—a new class of luminescent organometallic dinucleoside phosphate mimics. Issue 6 (19th January 2023)

• Record Type: Journal Article
• Authors: Skiba, Joanna; Kowalczyk, Aleksandra; Gorski, Aleksander; Dutkiewicz, Natalia; Gapińska, Magdalena; Stróżek, Józef; Woźniak, Krzysztof; Trzybiński, Damian; Kowalski, Konrad
• Is Part Of: Dalton transactions. Volume 52:Issue 6(2023)
• Page Start: 1551
• Page End: 1567
• Publication Date: 2023-01-19
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d2dt03995h
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : A "click" synthetic approach toward first-in-class dinucleoside phosphate mimics possessing a luminescent dirhenium carbonyl linker instead of a phosphodiester entity is reported. Abstract : The first-in-class luminescent dinucleoside phosphate analogs with a [Re2 (μ-Cl)2 (CO)6 (μ-pyridazine)] "click" linker as a replacement for the natural phosphate group are reported together with the synthesis of luminescent adenosine and thymidine derivatives having the [Re2 (μ-Cl)2 (CO)6 (μ-pyridazine)] entity attached to positions 5′ and 3′, respectively. These compounds were synthesized by applying inverse-electron-demand Diels–Alder and copper(i )-catalyzed azide–alkyne 1, 3-dipolar cycloaddition reactions in three or four steps. The obtained compounds exhibited orange emission ( λ PL ≈ 600 nm, Φ PL ≈ 0.10, and τ = 0.33–0.61 μs) and no toxicity (except for one nucleoside) to human HeLa cervical epithelioid and Ishikawa endometrial adenocarcinoma cancer cells in vitro . Furthermore, the compounds' ability to inhibit the growth of Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli bacterial strains was moderate and only observed at a high concentration of 100 μM. Confocal microscopy imaging revealed that the "dirhenium carbonyl" dinucleosides and nucleosides localized mainly in the membranous structures of HeLa cells and uniformly inside S. aureus and E. coli bacterial cells. An interesting finding was that some of the tested compounds were also found in the nuclei of HeLa cells.