A Study on Repositioning Nalidixic Acid via Lanthanide Complexation: Synthesis, Characterization, Cy...
A Study on Repositioning Nalidixic Acid via Lanthanide Complexation: Synthesis, Characterization, Cytotoxicity and DNA/Protein Binding Studies
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Basel: MDPI AG
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English
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Basel: MDPI AG
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“Drug repositioning” is a modern strategy used to uncover new applications for out-of-date drugs. In this context, nalidixic acid, the first member of the quinolone class with limited use today, has been selected to obtain nine new metal complexes with lanthanide cations (La3+, Sm3+, Eu3+, Gd3+, Tb3+); the experimental data suggest that the quinolo...
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A Study on Repositioning Nalidixic Acid via Lanthanide Complexation: Synthesis, Characterization, Cytotoxicity and DNA/Protein Binding Studies
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TN_cdi_doaj_primary_oai_doaj_org_article_2690ca2fe5dc477f90f6fe6cee8c5042
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2690ca2fe5dc477f90f6fe6cee8c5042
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1424-8247
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1424-8247
DOI
10.3390/ph15081010