Novel Alkylaminopyridazine Derivatives: Synthesis and Their Anti-proliferative Effects against MCF-7 Cells 


Vol. 34,  No. 11, pp. 3317-3321, Nov.  2013
10.5012/bkcs.2013.34.11.3317


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  Abstract

A series of new 3-alkylamino-6-allylthio-pyridazine derivatives was synthesized through allythiolation and amino-de-halogenation and were expected to have anti-proliferative activity. 6-Allylthio-3-chloropyridazine was prepared from the reaction of 3,6-dichloropyridazine with allylmercaptan and sodium hydroxide. The alkylamines such as methylamine and the dialkylamines such as dimethylamine were introduced into the 3- position of the pyridazine ring. These new compounds showed anti-proliferative activities against MCF-7 human breast cancer cells in CCK-8 assays. These compounds are thus promising candidates for chemotherapy of breast cancer. Two compounds, 14 and 15, showed higher potencies for inhibiting growth of breast cancer cells than did 5FU. This suggests the potential anti-proliferative activity of these compounds.

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  Cite this article

[IEEE Style]

C. Kim, E. Park, M. Park, "Novel Alkylaminopyridazine Derivatives: Synthesis and Their Anti-proliferative Effects against MCF-7 Cells," Bulletin of the Korean Chemical Society, vol. 34, no. 11, pp. 3317-3321, 2013. DOI: 10.5012/bkcs.2013.34.11.3317.

[ACM Style]

Chaewon Kim, Eun-Hee Park, and Myung-Sook Park. 2013. Novel Alkylaminopyridazine Derivatives: Synthesis and Their Anti-proliferative Effects against MCF-7 Cells. Bulletin of the Korean Chemical Society, 34, 11, (2013), 3317-3321. DOI: 10.5012/bkcs.2013.34.11.3317.

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ISSN(Print) 0253-2964
ISSN(Online) 1229-5949