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A new look at 9-substituted acridines with various biological activities
M. Kozurkova, D. Sabolova, P. Kristian
Language English Country Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
32969520
DOI
10.1002/jat.4072
Knihovny.cz E-resources
- MeSH
- Acridines chemistry pharmacology toxicity MeSH
- Anti-Bacterial Agents chemistry pharmacology toxicity MeSH
- Antimalarials chemistry pharmacology toxicity MeSH
- Topoisomerase II Inhibitors chemistry pharmacology toxicity MeSH
- Humans MeSH
- Tumor Cells, Cultured drug effects MeSH
- Antineoplastic Agents chemistry pharmacology toxicity MeSH
- Structure-Activity Relationship MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
Heterocycles have long been the focus of intensive study in attempts to develop novel therapeutic compounds, and acridine, a polynuclear nitrogen molecule containing a heterocycle, has attracted a considerable amount of scientific attention. Acridine derivatives have been studied in detail and have been found to possess multitarget properties, which inhibit topoisomerase enzymes that regulate topological changes in DNA and interfere with the essential biological function of DNA. This article describes some recent advancements in the field of new 9-substituted acridine heterocyclic agents and describes both the structure and the structure-activity relationship of the most promising molecules. The article will also present the IC50 values of the novel derivatives against various human cancer cell lines. The mini review also investigates the topoisomerase inhibition and antibacterial and antimalarial activity of these polycyclic aromatic derivatives.
References provided by Crossref.org
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- $a Kozurkova, Maria $u Department of Biochemistry, Institute of Chemistry, Faculty of Science, P. J. Šafárik University, Kosice, Slovak Republic $u Biomedical Research Center, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic
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- $a Heterocycles have long been the focus of intensive study in attempts to develop novel therapeutic compounds, and acridine, a polynuclear nitrogen molecule containing a heterocycle, has attracted a considerable amount of scientific attention. Acridine derivatives have been studied in detail and have been found to possess multitarget properties, which inhibit topoisomerase enzymes that regulate topological changes in DNA and interfere with the essential biological function of DNA. This article describes some recent advancements in the field of new 9-substituted acridine heterocyclic agents and describes both the structure and the structure-activity relationship of the most promising molecules. The article will also present the IC50 values of the novel derivatives against various human cancer cell lines. The mini review also investigates the topoisomerase inhibition and antibacterial and antimalarial activity of these polycyclic aromatic derivatives.
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