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Cytotoxicities, cell cycle and caspase evaluations of 1,6-diaryl-3(Z)-hexen-1,5-diynes, 2-(6-aryl-3(Z)-hexen-1,5-diynyl)anilines and their derivatives.

作者信息

Lin Chi-Fong, Lo Yu-Hsiang, Hsieh Ming-Chu, Chen Yi-Hua, Wang Jeh-Jeng, Wu Ming-Jung

机构信息

Department of Biological Science and Technology, Chung Hwa College of Medical Technology, Taiwan, Taiwan.

出版信息

Bioorg Med Chem. 2005 May 16;13(10):3565-75. doi: 10.1016/j.bmc.2005.02.062.

DOI:10.1016/j.bmc.2005.02.062
PMID:15848769
Abstract

Compounds 3, 6-7, 9-10, 15-17, and 20-21 showed growth inhibition effects on a full panel of 60 human cancer cell lines, and most of the average IC50 values of the indicated analogues were from < 0.01 to 96.6 microM, in which analogues 16 and 17 revealed the highest cytotoxic activity with the cancer cell lines at 10(-7) M concentration range. During the cell cycle analysis, a moderate to high apoptotic progress induction was shown by 3, 9, 16-17, and 20 compared with the control, which 2-(6-(2-thienyl)-3(Z)-hexen-1,5-diynyl)aniline 16 showed the highest apoptotic effect. Structures 16-17 displayed a significant G2/M phase arrest in the cell growth cycle compared with other derivatives, which the proportions of the G2/M phase cells were accumulated to 71.5% and 82.6%, respectively. Moreover, the colorimetric assay of 16-17 also provided advanced evidence to the relationship between the compounds and the caspase-3 enzyme, which was one of the major promoters of apoptotic effect.

摘要

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