1, 6-Diaryl-3(Z)-hexen-l, 5-diynes as Antitumor Agents

CNU IR > Pharmacy and Science > 2011 Taiwanese-Russian Organic, Medicinal and Bio Chemistry Interactions & PST Medicinal Chemistry Symposium > Item 310902800/24210

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Title:	1, 6-Diaryl-3(Z)-hexen-l, 5-diynes as Antitumor Agents
Authors:	Ming-Jung Wu (吳明忠)
Date:	2011
Issue Date:	2011-06-23 14:57:04 (UTC+8)
Abstract:	A series of l,5-diaryl-3(Z)-hexen-l,5-diynes have been synthesized and the growth inhibition activity against various human tumor ce ell lineies havive also been evaluated. 2-(6-(2-Trifluoromethylphenyl))-3(Z)-hexen-l,5-diynyl)aniline (1) was found to show high potency of growth inhibition activity. After a 24 h treatment with ompound 1, a strong ability to induce a massive accumulation of cells in the G2/M phase was observed. After 72 h treatment with compound 1, some of the cells undergo apoptosis via activation of caspase-3, -8 and -9. A brief exposure of the MDA-MB-231/ATCC cells to compound 1 is sufficient to produce sustained de-polymerization of the microtubules in a concentration-dependent manner. The disruption of microtubule is reversible when the drug is removed, which indicates a lower toxicity of this compound. The ligand docking experiment shows that ompound 1 binds to the α- and β-tubuline in the same manner as colchicine. The trifluoromethylphenyl group of 1 coincides with the trimethoxyphenyl subsunit of cholchicine and the amino group of 1 serves a hydrogen bond acceptor with α-tubulin (179-Thr and 181-Val), similar to the carbonyl group of colchicine. Replacing the ortho-trifluoromethylphenyl ring of compound 1 to 3,4,5-trimethoxyphenyl group gave compound 2. Compound 2 was found to exhibit even higher potency of growth inhibition activity against some human cancer cell lines.
Relation:	2011年台俄有機、藥物與生物化學交流暨藥物化學研討會，起迄日：2011/04/06~2011/04/05，地點：溪頭台大實驗林
Appears in Collections:	[Pharmacy and Science] 2011 Taiwanese-Russian Organic, Medicinal and Bio Chemistry Interactions & PST Medicinal Chemistry Symposium

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