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Molecules ; 29(1)2024 Jan 02.
Artigo em Inglês | MEDLINE | ID: mdl-38202823

RESUMO

Quercetin is a flavonoid with significant biological and pharmacological activity. In this paper, quercetin was modified at the 3-OH position. Rutin was used as a raw material. We used methyl protection, Williamson etherification reactions, and then substitution reactions to prepare 15 novel quercetin derivatives containing a quinoline moiety. All these complexes were characterized by 1H NMR, 13C NMR, IR and HRMS. Of these, compound 3e (IC50 = 6.722 µmol·L-1) had a better inhibitory effect on human liver cancer (HepG-2) than DDP (Cisplatin) (IC50 = 26.981 µmol·L-1). The mechanism of the action experiment showed that compound 3e could induce cell apoptosis.


Assuntos
Quercetina , Quinolinas , Humanos , Quercetina/farmacologia , Flavonoides , Quinolinas/farmacologia , Rutina , Analgésicos Opioides
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