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Bioorg Med Chem ; 21(22): 6920-8, 2013 Nov 15.
Article in English | MEDLINE | ID: mdl-24103429

ABSTRACT

This paper reports the synthesis of a series of evodiamine derivatives. We assayed the ability to inhibit cell growth on three human tumour cell lines (H460, MCF-7 and HepG2) and we evaluated the capacity to interfere with the catalytic activity of topoisomerase I both by the relaxation assay and the occurrence of the cleavable complex. Moreover, whose effect on sirtuins 1, 2 and 3 was investigated. Finally, molecular docking analyses were performed in an attempt to rationalize the biological results.


Subject(s)
DNA Topoisomerases, Type I/chemistry , Quinazolines/chemistry , Sirtuins/antagonists & inhibitors , Topoisomerase I Inhibitors/chemistry , Alkaloids/chemistry , Binding Sites , Carbolines/chemistry , Cell Line, Tumor , Cell Proliferation/drug effects , DNA Topoisomerases, Type I/metabolism , Enzyme Activation/drug effects , Hep G2 Cells , Humans , MCF-7 Cells , Molecular Docking Simulation , Protein Structure, Tertiary , Quinazolines/chemical synthesis , Quinazolines/pharmacology , Sirtuins/metabolism , Topoisomerase I Inhibitors/chemical synthesis , Topoisomerase I Inhibitors/pharmacology
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