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• W1975654310 abstract "Novel pyridine, thiophene, thiazole, chromene and benzochromene derivatives bearing a N,N-dimethylbenzenesulfonamide moiety 6–20 were synthesized. The target compounds were obtained through employing a series of heterocyclization reactions utilizing the key intermediate hydrazide hydrazone derivative 3. The structures of the newly synthesized compounds were confirmed by elemental analyses, IR, 1H-NMR and 13C-NMR spectral data. All the newly synthesized compounds were evaluated for their in vitro antiproliferative activity against the human breast cancer cell line MCF-7. Biological screening results showed that sulfonamides 6, 9, 11, 16 and 17 with IC50 values 21.81, 25.50, 20.60, 25.83 and 31.20 μM, respectively, possessed higher antiproliferative activity compared to doxorubicin, IC50 value 32.00 μM, as position control. Molecular docking study was also performed to assess the binding mode of the synthesized sulfonamides with their potential biomolecular target, carbonic anhydrase IX (CA IX), which is usually highly expressed in some types of cancer cells." @default.
• W1975654310 created "2016-06-24" @default.
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• W1975654310 date "2013-10-03" @default.
• W1975654310 modified "2023-09-24" @default.
• W1975654310 title "Design, synthesis and molecular docking of novel<i>N,N</i>-dimethylbenzenesulfonamide derivatives as potential antiproliferative agents" @default.
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• W1975654310 doi "https://doi.org/10.3109/14756366.2013.833197" @default.
• W1975654310 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24090422" @default.
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