Antiproliferative activity of 2-alkyl-4-halopiperidines and 2-alkyl-4-halo-1,2,5,6-tetrahydropyridines in solid tumor cell lines
A series of trans-2-alkyl-4-halopiperidines and 2-alkyl-4-halo-1,2,5,6-tetrahydropyridines were prepared by means of an iron(III) catalyzed process. The in vitro antiproliferative activities were examined in the human solid tumor cell lines A2780 (ovarian cancer), SW1573 (non-small cell lung cancer), and WiDr (colon cancer). The results on the biological activity revealed that, in general, the 2-alkyl-4-halo-1,2,5,6-tetrahydropyridine analogs are more potent than the trans-2-alkyl-4-halopiperidine derivatives. A remarkable selectivity of the aza compound 5f for the resistant cell line WiDr was observed. Cell cycle studies revealed a G2/M phase arrest for 5f.
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Main Authors: | León, Leticia G., Carballo, Rubén M., Vega-Hernández, María C., Martín, Víctor S., Padrón, Juan I., Padrón, José M. |
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Other Authors: | Ministerio de Educación y Ciencia (España) |
Format: | artículo biblioteca |
Language: | English |
Published: |
Elsevier
2007-05-17
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Subjects: | Marine drugs, Anticancer drugs, Halogenated piperidines, Halogenated tetrahydropyridines, Solid tumors, Structure–activity relationship, |
Online Access: | http://hdl.handle.net/10261/212239 |
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