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Molecules ; 27(16)2022 Aug 17.
Article in English | MEDLINE | ID: mdl-36014478

ABSTRACT

In the present study, new 2-phenyl-5,6,7,8-tetrahydroimidazo [1,2-b]pyridazines bearing sulfonamides were synthesized, characterized and evaluated for their anticancer activities. The structures of these derivatives were elucidated by 1H NMR, 13C NMR, infrared and high-resolution mass spectrometry for further validation of the target compound structures. The anticancer activities of the new molecules were evaluated against five human cancer cell lines, including A-549, Hs-683, MCF-7, SK-MEL-28 and B16-F10 cell lines using 5-fluorouracil and etoposide as the reference drugs. Among the tested compounds, 4e and 4f exhibited excellent activities in the same range of the positive controls, 5-fluorouracil and etoposide, against MCF-7 and SK-MEL-28 cancer cell lines, with IC50 values ranging from 1 to 10 µM. The molecular docking studies of 4e and 4f showed a strong binding with some kinases, which are linked to MCF-7 and SK-MEL-28 cancer cell lines.


Subject(s)
Antineoplastic Agents , Neoplasms , Pyridazines , Antineoplastic Agents/chemistry , Cell Line, Tumor , Cell Proliferation , Drug Screening Assays, Antitumor , Etoposide/pharmacology , Fluorouracil/pharmacology , Humans , Molecular Docking Simulation , Molecular Structure , Neoplasms/drug therapy , Pyridazines/chemistry , Structure-Activity Relationship , Sulfanilamide/pharmacology , Sulfonamides/pharmacology , Sulfonamides/therapeutic use
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