Synthesis and antitumor activity of amino acid ester derivatives containing 5-fluorouracil

26Citations
Citations of this article
26Readers
Mendeley users who have this article in their library.

Abstract

A series of amino acid ester derivatives containing 5-fluorouracil were synthesized using 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC-HCl) and N-hydroxybenzotriazole (HOBt) as a coupling agent. The structures of the products were assigned by NMR, MS, IR etc. The in vitro antitumor activity tests against leukaemia HL-60 and liver cancer BEL-7402 indicated that (R)-ethyl 2-(2-(5-fluoro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetamido)-3- (4-hydroxyphenyl) propanoate showed more inhibitory effect against BEL-7402 than 5-FU. © 2009 by the authors.

Cite

CITATION STYLE

APA

Xiong, J., Zhu, H. F., Zhao, Y. J., Lan, Y. J., Jiang, J. W., Yang, J. J., & Zhang, S. F. (2009). Synthesis and antitumor activity of amino acid ester derivatives containing 5-fluorouracil. Molecules, 14(9), 3142–3152. https://doi.org/10.3390/molecules14093142

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