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The accumulation of iron in dopaminergic neurons can cause oxidative stress and dopaminergic neuron degeneration. Iron chelation therapy may reduce dopaminergic neurodegeneration, but chelators should be targeted towards dopaminergic cells. In this work, two series of compounds based on 8-hydroxyquinoline and deferiprone, iron chelators that have amphetamine-like structures, have been designed, synthesized and characterized. Each of these compounds chelated iron ions in aqueous solution. The hydroxyquinoline-based compounds exhibited stronger iron-binding constants than those of the deferiprone derivatives. The hydroxyquinoline-based compounds also exhibited greater free radical scavenging activities compared to the deferiprone derivatives. Molecular dynamics simulations showed that the hydroxyquinoline-based compounds generally bound well within human dopamine transporter cavities. Thus, these compounds are excellent candidates for future exploration as drugs against diseases that are affected by iron-induced dopaminergic neuron damage, such as Parkinson's disease.
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http://dx.doi.org/10.3390/molecules29174213 | DOI Listing |
Dalton Trans
August 2025
Guangxi Key Laboratory of Agricultural Resources Chemistry and Biotechnology, College of Chemistry and Food Science, Yulin Normal University, 1303 Jiaoyudong Road, Yulin 537000, PR China.
To develop novel calcium(II) coordination compounds aimed at overcoming cisplatin (RiPt) resistance, we synthesized three dinuclear calcium(II) complexes: [Ca(μ-O)(dhg1)(CP)] (CaL1), [Ca(μ-O)(dhg2)(CP)] (CaL2), and [Ca(μ-O)(dhg3)(CP)] (CaL3). These contain four deprotonated 5,7-dichloro-8-quinolinol (H-dhg1), clioquinol (H-dhg2), or 5,7-dibromo-8-hydroxyquinoline (H-dhg3) ligands, respectively, and two 5-chloro-1,10-phenanthroline (CP) ligands. cytotoxicity studies of CaL1-CaL3 against cisplatin-resistant ovarian SK-OV-3/DDP (RiSK3) cancer cells and healthy (HL-7702) cells revealed promising selective cytotoxicity toward RiSK3 cells with IC values of 0.
View Article and Find Full Text PDFRSC Adv
January 2025
Third World Center for Science and Technology, H. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi Karachi 75270 Pakistan
A new series of sensitive 8-hydroxyquinoline azo-compounds (S1-S8) as sensors was synthesized by diazotization and diazo-coupling, and these compounds were characterized through UV, FTIR, H-NMR, C-NMR and ESI-MS investigations. The UV-visible spectral data revealed that Ni was sensed by compounds S2, S3, S4, and S6, producing colour changes ranging from violet to orange, and exhibited bathochromism of +8, +67, +63, and +85 nm, respectively. Optimized conditions included a mixture of ethanol/water (4 : 1) solvent system; pH 4 for compounds S3, S4, and S6, and pH 8 for compound S2; reaction time of 2 min; and a stoichiometric ratio of 3 : 1.
View Article and Find Full Text PDFMolecules
September 2024
School of Mathematical and Physical Sciences, Faculty of Science, University of Technology Sydney, Sydney, NSW 2007, Australia.
The accumulation of iron in dopaminergic neurons can cause oxidative stress and dopaminergic neuron degeneration. Iron chelation therapy may reduce dopaminergic neurodegeneration, but chelators should be targeted towards dopaminergic cells. In this work, two series of compounds based on 8-hydroxyquinoline and deferiprone, iron chelators that have amphetamine-like structures, have been designed, synthesized and characterized.
View Article and Find Full Text PDFInorg Chem
September 2022
Molecular and Environmental Sciences Group, Department of Geological Sciences, College of Arts and Science, University of Saskatchewan, 114 Science Place, Saskatoon, SaskatchewanS7N 5E2, Canada.
Although Alzheimer's disease (AD) was first described over a century ago, it remains the leading cause of age-related dementia. Innumerable changes have been linked to the pathology of AD; however, there remains much discord regarding which might be the initial cause of the disease. The "amyloid cascade hypothesis" proposes that the amyloid β (Aβ) peptide is central to disease pathology, which is supported by elevated Aβ levels in the brain before the development of symptoms and correlations of amyloid burden with cognitive impairment.
View Article and Find Full Text PDFChemMedChem
March 2022
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Ljubljana, Askerceva 7, 1000, Ljubljana, Slovenia.
A library of 31 butyrylcholinesterase (BChE) and cathepsin B (CatB) inhibitors was screened in vitro for inhibition of deoxyribonuclease I (DNase I). Compounds 22, 8 and 7 are among the most potent synthetic non-peptide DNase I inhibitors reported to date. Three 8-hydroxyquinoline analogues inhibited both DNase I and BChE with IC values below 35 μM and 50 nM, respectively, while two nitroxoline derivatives inhibited DNase I and Cat B endopeptidase activity with IC values below 60 and 20 μM.
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