| Literature DB >> 33479625 |
Mabel Catalán1, Vicente Castro-Castillo2, Javier Gajardo-de la Fuente2, Jocelyn Aguilera3, Jorge Ferreira1, Ricardo Ramires-Fernandez4, Ivonne Olmedo5, Alfredo Molina-Berríos3, Charlotte Palominos1, Marcelo Valencia1, Marta Domínguez6, José A Souto6, José A Jara3.
Abstract
Continuous flow chemistry was used for the synthesis of a series of delocalized lipophilic triphenylphosphonium cations (DLCs) linked by means of an ester functional group to several hydroxylated benzoic acid derivatives and evaluated in terms of both reaction time and selectivity. The synthesized compounds showed cytotoxic activity and selectivity in head and neck tumor cell lines. The mechanism of action of the molecules involved a mitochondrial uncoupling effect and a decrease in both intracellular ATP production and apoptosis induction. This journal is © The Royal Society of Chemistry 2020.Entities:
Year: 2020 PMID: 33479625 PMCID: PMC7652000 DOI: 10.1039/d0md00153h
Source DB: PubMed Journal: RSC Med Chem ISSN: 2632-8682