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Bioorg Chem ; 59: 130-9, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25771335

ABSTRACT

A new series of DNA-interactive ß-carboline-chalcone conjugates have been synthesized and evaluated for their in vitro cytotoxicity and DNA-binding affinity. It has been observed that most of these new hybrids have shown potent cytotoxic activities on A-549 (lung adenocarcinoma) cell lines with IC50 values lower than 10 µM. The hybrid 7b is more effective against some of the selected cancer cell lines with IC50 values less than 50 µM. In addition, compounds 7e, 7k, 7p-u has displayed significant elevation in ΔTm of DNA in comparison to Adriamycin, suggesting significant interaction and remarkable DNA stabilization. The DNA intercalation of these new hybrids has been investigated by fluorescence titration, DNA viscosity measurements, molecular docking as well as molecular dynamics and the results are in agreement with the thermal denaturation studies.


Subject(s)
Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Carbolines/chemistry , Carbolines/pharmacology , Chalcone/chemistry , Chalcone/pharmacology , Cell Line, Tumor , Cell Proliferation/drug effects , DNA/metabolism , Drug Screening Assays, Antitumor , Humans , Intercalating Agents/chemistry , Intercalating Agents/pharmacology , Models, Molecular , Neoplasms/drug therapy , Structure-Activity Relationship
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