Diacetate Naphthoquinone Derivatives Tethered to 1,2,3-Triazoles: Synthesis and Cytotoxicity Evaluation in Caco-2 Cells

Autor: Costa, Dora C. S., Francisco, Adriane S., Matuck, Beatriz V. A., Furtado, Priscila S., Oliveira, Alana A. S. C. de, Rabelo, Vitor W.-H., Sathler, Plínio C., Abreu, Paula A., Ferreira, Vitor F., Silva, Luiz Cláudio R. P. da, Silva, Fernando C. da

Publikováno v: Journal of the Brazilian Chemical Society v.33 n.1 2022
Journal of the Brazilian Chemical Society
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Journal of the Brazilian Chemical Society, Volume: 33, Issue: 1, Pages: 48-59, Published: 10 JAN 2022

Acetylated compounds prepared from naphthoquinones have been reported as antitumoral prodrugs. Exploring the synthetic versatility of the naphthoquinone and triazolic nuclei, herein we report a simple and efficient synthetic route to prepare a series

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::241dc58747d633befbf1b53dbb853cca
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532022000100048