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Updated: Dec 13, 2025

Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
2H-1,2,3-Triazole-chalcones as novel cytotoxic agents against prostate cancer
Sergio Pinheiro1, Jaqueline C Pessôa1, Erick M C Pinheiro2
1Chemistry Institute, Fluminense Federal University, Outeiro de S. João Batista s/n, Centro, 24020-141 Niterói, RJ, Brazil.
Abstract:
Prostate cancer is an important cause of death in the male population and for which there is no satisfactory chemotherapy. Herein a new series of chalcone hybrids containing 2H-1,2,3-triazole core as the ring B has been synthesized and evaluated in vitro against PC-3 prostate cancer cell line. Compounds 4a, 4c and 4e significantly reduced cell viability and showed IC50 of 28.55, 15.64 and 25.56 µM, respectively. The structure-activity relationship supported by computational chemistry points that the polarity of the molecular surface area should have some relevance to the efficiency of the compounds, in particular the ratio of the partial positive charge sites and the total molecular surface area exposed to the cell environment.
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