Design, synthesis and In Vitro cytotoxic activity evaluation of new mannich bases

18Citations
Citations of this article
18Readers
Mendeley users who have this article in their library.
Get full text

Abstract

A series of Novel Mannich bases has been synthesized and evaluated in vitro cytotoxic activity against the human hepatocellular carcinoma (HepG2), human lung carcinoma (SK-LU-1), and human breast cancer (MCF-7). Compound 9f was found to be most potent against three cell lines with IC50 values of 1.57, 1.16 and 1.21 μg/mL, respectively. In addition, compounds 9g, 10f exhibited very significant activity against MCF-7 cell line with IC50 values of 2.0 μg/mL. © 2005 KCSNET.

Cite

CITATION STYLE

APA

Hieu, B. T., Thuy, L. T., Thuy, V. T., Tien, H. X., Chinh, L. V., Hoang, V. D., & Vu, T. K. (2012). Design, synthesis and In Vitro cytotoxic activity evaluation of new mannich bases. Bulletin of the Korean Chemical Society, 33(5), 1586–1592. https://doi.org/10.5012/bkcs.2012.33.5.1586

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free