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Synthesis and anti-tumor activity of paeonol and its derivatives / 药学学报
Acta Pharmaceutica Sinica ; (12): 72-76, 2012.
Article de Zh | WPRIM | ID: wpr-323078
Bibliothèque responsable: WPRO
ABSTRACT
A series of paeonol derivatives have been synthesized by simple acylation and etherification of the paeonol. Anti-tumor activities of the synthesized compounds were evaluated against HeLa and MCF-7 cells lines in vitro by the standard MTT assay. It was found that the derivatives were more active against HeLa than MCF-7. The results also indicated that 4-methoxy group is the synergistic group of paeonol's anti-tumor activity and ketone carbonyl side chain is essential functional group of paeonol's anti-tumor activity. Compound 2d had stronger antiproliferative activities than paeonol against HeLa and MCF-7 cell lines with IC50 values of 2.67 and 4.74 micromol x L(-1) respectively. The results showed that paeonol derivatives were worth to be intensively studied further.
Sujet(s)
Texte intégral: 1 Indice: WPRIM Sujet Principal: Acétophénones / Pharmacologie / Relation structure-activité / Tests de criblage d'agents antitumoraux / Cellules HeLa / Chimie / Concentration inhibitrice 50 / Prolifération cellulaire / Cellules MCF-7 / Antinéoplasiques d'origine végétale Limites du sujet: Humans langue: Zh Texte intégral: Acta Pharmaceutica Sinica Année: 2012 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Acétophénones / Pharmacologie / Relation structure-activité / Tests de criblage d'agents antitumoraux / Cellules HeLa / Chimie / Concentration inhibitrice 50 / Prolifération cellulaire / Cellules MCF-7 / Antinéoplasiques d'origine végétale Limites du sujet: Humans langue: Zh Texte intégral: Acta Pharmaceutica Sinica Année: 2012 Type: Article