Synthesis and biological activity evaluation of hydrazone derivatives based on a Tröger's base skeleton
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25737088
DOI
10.1016/j.bmc.2015.01.029
PII: S0968-0896(15)00045-0
Knihovny.cz E-resources
- Keywords
- Anticancer agents, Cancer treatment, Complexation studies, Hydrazone, Tröger’s base,
- MeSH
- Antineoplastic Agents chemical synthesis pharmacology MeSH
- Apoptosis drug effects physiology MeSH
- K562 Cells MeSH
- HCT116 Cells MeSH
- Hydrazones chemical synthesis pharmacology MeSH
- Humans MeSH
- Drug Evaluation, Preclinical methods MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Antineoplastic Agents MeSH
- Hydrazones MeSH
We report the design and synthesis of novel anticancer agents based on bis-hydrazones separated by a rigid Tröger's base skeleton. This novel approach combines a biologically active moiety (hydrazone) with this scaffold (Tröger's base) to construct DNA intercalators. Evaluation of the anticancer activity of these agents using seven cancer cell lines and two healthy cell lines found that several derivatives had potent anticancer activity and excellent selectivity indexes toward cancer cells. The antimicrobial activities were tested on a set of thirteen bacterial stains, but the prepared compounds were not active. Complexation studies using biologically important metal ions demonstrated that these compounds are able to bind Cu(2+), Fe(3+), Co(2+), Ni(2+) and Zn(2+). DNA intercalation studies showed that the compounds themselves do not interact with DNA, but their metallocomplexes do interact, most likely via intercalation into DNA.
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