4.6 Article

Synthesis and in vitro cytotoxicity of deoxyadenosine-bile acid conjugates linked with 1,2,3-triazole

Journal

NEW JOURNAL OF CHEMISTRY
Volume 37, Issue 11, Pages 3559-3567

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3nj00513e

Keywords

-

Ask authors/readers for more resources

We report herein the synthesis and biological evaluation of novel deoxynucleoside-bile acid conjugates linked through a 1,2,3-triazole ring. The conjugates were synthesized via Cu(I) mediated 1,3-dipolar cycloaddition reaction ('click' chemistry) of 3-azidobile acid derivatives and terminal alkyne moieties linked to the C-8 position of deoxyadenosine. All novel molecules were evaluated in vitro for their anti-proliferative activity against four human cell lines (i.e., leukemic T Jurkat and K562; colon carcinoma HCT116; and ovarian cancer A2780) and their cytotoxicity toward human fibroblast cells. Several conjugates exhibited strong anti-proliferative activity against human leukemia T cells. The best cytotoxicity was observed for HdA-CDC on both leukemia cell lines with IC50 up to 8.51 mu M. The apoptotic activity of several conjugates was also established.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available