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Cobalt(III) compounds with tetradentate ligands have been widely employed to deliver cytotoxic and imaging agents into cells. A large body of work has focused on using cobalt(III)-cyclam scaffolds for this purpose. Here, we investigate the cytotoxic properties of cobalt(III) complexes containing 14-membered macrocycles related to cyclam. A breast cancer stem cell (CSC) in vitro model was used to gauge efficacy. Specifically, [Co(1,4,7,11-tetraazacyclotetradecane)Cl] () and [Co(1-oxa-4,8,12-triazacyclotetradecane)Cl] () were synthesised and characterised, and their breast CSC activity was determined. The cobalt(III) complexes and displayed micromolar potency towards bulk breast cancer cells and breast CSCs grown in monolayers. Notably, and displayed selective potency towards breast CSCs over bulk breast cancer cells (up to 4.5-fold), which was similar to salinomycin (an established breast CSC-selective agent). The cobalt(III) complexes and were also able to inhibit mammosphere formation at low micromolar doses (with respect to size and number). The mammopshere inhibitory effect of was similar to that of salinomycin. Our studies show that cobalt(III) complexes with 1,4,7,11-tetraazacyclotetradecane and 1-oxa-4,8,12-triazacyclotetradecane macrocycles could be useful starting points for the development of new cobalt-based delivery systems that can transport cytotoxic and imaging agents into breast CSCs.
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http://dx.doi.org/10.3390/molecules29122743 | DOI Listing |
Chemistry
August 2025
Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand, 247667, India.
In this report, we present a sustainable, eco-friendly, practical, and cost-effective one-pot three-component reaction for the synthesis of a diverse library of highly substituted pyrimidines from amidines, primary alcohols, and aromatic ketones, catalyzed by a cobalt(III) complex. The well-defined cobalt(III) complex [Co(III)BPMAP-O]ClO is derived from a redox-active phosphine-free, pentadentate mono-carboxamide ligand (BPMAP-H), and is formed in situ from various cobalt(II) sources, including CoCl·6HO, CoBr, Co(NO)·6HO, Co(OAc)·4HO via oxygen activation. Using aromatic ketones and benzyl alcohols, a wide range of 2,4,6-trisubstituted pyrimidines (TriPym) and 2,4,5,6-tetrasubstituted pyrimidines (TetraPym) were synthesized (119 examples) in isolated yields of up to 93%.
View Article and Find Full Text PDFChem Sci
September 2025
Department of Chemistry, Michigan State University East Lansing USA
Exploration of the photophysical and photochemical properties of transition metal complexes has driven ground-breaking advancements in solar energy conversion technologies, including photoredox catalysis. While significant research has been devoted to understanding excited state properties of second- and third-row transition metal complexes, earth-abundant first-row metal complexes have received comparatively little attention in this context until very recently. In particular, the role of ion-pairing - which has been identified as a potentially significant factor for Ir(iii)-based photosensitizers - has not been examined with regard to its influence on the ligand-field excited states that dominate much of first-row photophysics.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
Department of Chemistry, University of Basel, St. Johanns-Ring 19, Basel 4056, Switzerland.
Co complexes have recently become an important focus in photophysics and photoredox catalysis due to metal-centered excited states with strong oxidizing properties. Optimizing chelate ligand bite angles is a widely used strategy to strengthen metal-ligand interactions in coordination complexes, with the resulting enhanced ligand fields often contributing to extended excited-state lifetimes that are advantageous for photochemical applications. We demonstrate that bite-angle optimization exerts the opposite effect on Co polypyridines compared to previously studied transition metal complexes, as polypyridine ligands function as π-donors to Co rather than π-acceptors.
View Article and Find Full Text PDFAnal Methods
August 2025
Key Laboratory for Functional Material, Educational Department of Liaoning Province, University of Science and Technology Liaoning, Anshan, Liaoning Province 114051, P. R. China.
A fluorescence/magnetic resonance (MR) dual-mode molecular probe H1 based on cobalt(III) complexes was designed and synthesized in this work for the detection of sodium dithionite (NaSO) and real-time biological imaging . The probe combines highly sensitive fluorescence imaging technology and high-resolution magnetic resonance imaging (MRI) technology to address the limitations of each individual modality. Probe H1 used Co as the MRI unit and 3-acetylacetone-7-diethylamino-coumarin as the fluorescence unit.
View Article and Find Full Text PDFNat Commun
July 2025
Fachbereich Chemie, Philipps-Universität Marburg, Marburg, Germany.
For decades, progress in chiral transition metal catalysis has been closely linked to the design of tailor-made chiral ligands. Recently, an alternative to this conventional paradigm has emerged in which the overall chirality of the catalysts arises solely from a stereogenic metal center. However, the development of such chiral-at-metal catalysts based on earth-abundant metals is still a formidable challenge.
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