Quinoline-based antifungals
- PMID: 20377510
- DOI: 10.2174/092986710791163966
Quinoline-based antifungals
Abstract
Although the assortment of antifungal drugs is broad, the most commonly used agents have major drawbacks. Toxicity, serious side effects or the emergence of drug resistance are amongst them. New drugs and drug candidates under clinical trials do not guarantee better pharmacological parameters. These new medicines may appear effective; however; they may cause serious side effects. This current review is focused on the recent findings in the design of quinoline based antifungal agents. This field seems to be especially interesting as 8-hydroxyquinoline and its metal complexes have been well known as antifungals for years. Structural similarities between quinoline based antifungals and allylamines or homoallylamines, e.g. terbinafine is another interesting fact. Quinoline can be identified in a number of synthetic and natural antifungals, which indicates nature's preference for this fragment and identifying it as one of the so-called privileged structures. We have discussed new trends in the design of quinolines with antifungal properties, their possible targets and the structure activity relationships within the antifungal series developed.
Similar articles
-
Recent update on antibacterial and antifungal activity of quinoline scaffolds.Arch Pharm (Weinheim). 2021 Mar;354(3):e2000232. doi: 10.1002/ardp.202000232. Epub 2020 Nov 19. Arch Pharm (Weinheim). 2021. PMID: 33210348 Review.
-
Tetrazole hybrids and their antifungal activities.Eur J Med Chem. 2019 May 15;170:225-234. doi: 10.1016/j.ejmech.2019.03.023. Epub 2019 Mar 15. Eur J Med Chem. 2019. PMID: 30904780 Review.
-
Antifungals discovery: an insight into new strategies to combat antifungal resistance.Lett Appl Microbiol. 2018 Jan;66(1):2-13. doi: 10.1111/lam.12820. Epub 2017 Dec 11. Lett Appl Microbiol. 2018. PMID: 29112282 Review.
-
Evaluation of (4-aminobutyloxy)quinolines as a novel class of antifungal agents.Bioorg Med Chem Lett. 2013 Aug 15;23(16):4641-3. doi: 10.1016/j.bmcl.2013.06.014. Epub 2013 Jun 13. Bioorg Med Chem Lett. 2013. PMID: 23838261
-
Quinoline derivatives bearing pyrazole moiety: Synthesis and biological evaluation as possible antibacterial and antifungal agents.Eur J Med Chem. 2018 Jan 1;143:1463-1473. doi: 10.1016/j.ejmech.2017.10.046. Epub 2017 Oct 19. Eur J Med Chem. 2018. PMID: 29113746
Cited by
-
Development of Efficient Covalent Inactivators of a Fungal Aspartate Semialdehyde Dehydrogenase.Drug Dev Res. 2025 May;86(3):e70095. doi: 10.1002/ddr.70095. Drug Dev Res. 2025. PMID: 40341627 Free PMC article.
-
Evaluation of Alkaloids Isolated from Ruta graveolens as Photosynthesis Inhibitors.Molecules. 2018 Oct 19;23(10):2693. doi: 10.3390/molecules23102693. Molecules. 2018. PMID: 30347671 Free PMC article.
-
Investigation of Novel Quinoline-Thiazole Derivatives as Antimicrobial Agents: In Vitro and In Silico Approaches.ACS Omega. 2022 Dec 29;8(1):1410-1429. doi: 10.1021/acsomega.2c06871. eCollection 2023 Jan 10. ACS Omega. 2022. PMID: 36643421 Free PMC article.
-
Uracil as a Zn-Binding Bioisostere of the Allergic Benzenesulfonamide in the Design of Quinoline-Uracil Hybrids as Anticancer Carbonic Anhydrase Inhibitors.Pharmaceuticals (Basel). 2022 Apr 19;15(5):494. doi: 10.3390/ph15050494. Pharmaceuticals (Basel). 2022. PMID: 35631321 Free PMC article.
-
Facile synthesis and in vitro anticancer evaluation of a new series of tetrahydroquinoline.Heliyon. 2021 Oct 4;7(10):e08117. doi: 10.1016/j.heliyon.2021.e08117. eCollection 2021 Oct. Heliyon. 2021. PMID: 34693052 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical