Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1397337 | European Journal of Medicinal Chemistry | 2014 | 7 Pages |
•Novel spiropyrazoline oxindole derivatives were synthesized.•Compounds were evaluated against MCF-7 and MDA-MB-231 breast cancer cell lines.•Two spiropyrazoline oxindoles presented much higher potency against MCF-7 tumor cells than against MDA-MB-231 tumor cells.•The most active compounds were noncytotoxic against HEK 293T.
A series of novel spiropyrazoline oxindole derivatives was synthesized by 1,3-dipolar cycloaddition reaction. The compounds were screened for their in vitro cytotoxic activity against MCF-7 breast cancer cell line (estrogen receptor positive (ER+) and human epidermal growth factor receptor 2 negative (HER2−)). Of the nineteen spiropyrazoline oxindoles tested, six compounds have a GI50 below 12 μM The most potent compounds in this series were also evaluated against MDA-MB-231 breast cancer cell line (ER− and HER2−). Two spiropyrazoline oxindoles were highly selective between MCF-7 tumor cells and MDA-MB-231 tumor cells. More importantly, they were noncytotoxic against HEK 293T non tumor derived cell lines.
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