To cite this paper use one of the standards below:
The objective was to synthesize different esters from the 3α and 3β isomers of the triterpene friedelinol and evaluate their anti-leukemic and anticholinesterase activities. Eight esters were synthesized. All of them showed low anti-leukemic activity against the THP-1 and K-562 cell lines. Overall, all esters exhibited good percentages of acetylcholinesterase inhibition at least at one of the tested concentrations.
With nearly 200,000 papers published, Galoá empowers scholars to share and discover cutting-edge research through our streamlined and accessible academic publishing platform.
Learn more about our products:
This proceedings is identified by a DOI , for use in citations or bibliographic references. Attention: this is not a DOI for the paper and as such cannot be used in Lattes to identify a particular work.
Check the link "How to cite" in the paper's page, to see how to properly cite the paper