Vanadium 8-hydroxyquinoline derivatives in medicine: current state and future outlook
- PMID: 40329148
- DOI: 10.1007/s10534-025-00683-9
Vanadium 8-hydroxyquinoline derivatives in medicine: current state and future outlook
Abstract
Vanadium complexes featuring 8-hydroxyquinoline ligands and their derivatives have emerged as a promising class of compounds with potential therapeutic applications, particularly as antimicrobial and anticancer agents. This comprehensive review offers a timely and insightful analysis of the current landscape of vanadium complexes with HQ ligand or its derivatives, whether alone or in combination with organic coligands. This review covers synthetic strategies, and mechanisms that underlie their antibacterial and anticancer activities. A significant focus of this review is the thorough evaluation of the antibacterial and anticancer properties of these complexes, providing an invaluable resource for researchers in the interdisciplinary fields of inorganic chemistry, medicinal chemistry, and drug discovery. By compiling and synthesizing the existing knowledge on vanadium-8-hydroxyquinoline (VO-8HQ) complexes, this review addresses a critical gap in the literature. Ongoing research, including rigorous preclinical and clinical evaluations, is essential for fully exploring the therapeutic potential of this promising class of metallodrugs.
Keywords: Antibacterial activity; Antibacterial and anticancer mechanisms; Anticancer activity; Synthetic strategies; Toxicity; Vanadium-8-hydroxyquinoline complexes.
© 2025. The Author(s), under exclusive licence to Springer Nature B.V.
Conflict of interest statement
Declarations. Conflict of interest: The authors declare no competing interests.
Similar articles
-
In vitro antiproliferative effect of vanadium complexes bearing 8-hydroxyquinoline-based ligands - the substituent effect.Dalton Trans. 2020 May 26;49(20):6596-6606. doi: 10.1039/d0dt01017k. Dalton Trans. 2020. PMID: 32342090
-
Vanadium(IV) Complexes with Methyl-Substituted 8-Hydroxyquinolines: Catalytic Potential in the Oxidation of Hydrocarbons and Alcohols with Peroxides and Biological Activity.Molecules. 2021 Oct 21;26(21):6364. doi: 10.3390/molecules26216364. Molecules. 2021. PMID: 34770772 Free PMC article.
-
Heteroleptic Oxidovanadium(V) Complexes with Activity against Infective and Non-Infective Stages of Trypanosoma cruzi.Molecules. 2021 Sep 3;26(17):5375. doi: 10.3390/molecules26175375. Molecules. 2021. PMID: 34500808 Free PMC article.
-
Insights of 8-hydroxyquinolines: A novel target in medicinal chemistry.Bioorg Chem. 2021 Mar;108:104633. doi: 10.1016/j.bioorg.2021.104633. Epub 2021 Jan 12. Bioorg Chem. 2021. PMID: 33513476 Review.
-
Vanadium complexes with polypyridyl ligands: Speciation, structure and potential medicinal activity.J Inorg Biochem. 2022 Apr;229:111712. doi: 10.1016/j.jinorgbio.2022.111712. Epub 2022 Jan 10. J Inorg Biochem. 2022. PMID: 35065318 Review.
References
-
- Abu-dief AM, Mohamed IMA (2015) A review on versatile applications of transition metal complexes incorporating Schiff bases. J Basic Appl Sci 4(2):119–133. https://doi.org/10.1016/j.bjbas.2015.05.004 - DOI
-
- Agents A, Fu H, Li Z, Hu X, Si S, You X, Tang S (2019) Synthesis and biological evaluation of quinoline derivatives as a novel class of broad-spectrum. Molecules 24:548. https://doi.org/10.3390/molecules24030548 - DOI
-
- Amini MM, Mohammadnezhad G (2012) Synthesis, crystal structure, and spectroscopic behavior of 8-hydroxyquinolato oxoalkoxo vanadium (V) complexes. J Coord Chem 65(2014):2945–2956. https://doi.org/10.1080/00958972.2012.707317 - DOI
-
- Be C, Laras Y, Moret V, Marcowycz A, Lamoral-theys D, Dubois J, Barthelemy-requin M, Kiss R, Depauw S, Cresteil T (2010) Structure–activity relationships and mechanism of action of antitumor bis 8-hydroxyquinoline substituted benzylamines. Eur J Med Chem 45:623–638. https://doi.org/10.1016/j.ejmech.2009.11.006 - DOI
-
- Ben D, Kahana N, Kampel V, Warshawsky A, Youdim MBH (2004) Neuroprotection by a novel brain permeable iron chelator, VK-28, against 6-hydroxydopamine lession in rats. Neuropharmacology 46:254–263. https://doi.org/10.1016/j.neuropharm.2003.09.005 - DOI
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous