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Acta Pharmaceutica Sinica ; (12): 574-578, 2015.
Artículo en Chino | WPRIM | ID: wpr-257099

RESUMEN

N-Benzyl matrinol was obtained by hydrolysis, benzylation and reduction reaction from matrine. A series of hybrids (8a-8n) from (phenylsulfonyl)furoxan and N-benzyl matrinol were synthesized and biologically evaluated as anti-hepatocellular carcinoma agents. All target compounds were evaluated for anti-proliferative activity against human hepatocellular Bel-7402, SMMC-7721, Bel-7404, and HepG2 cells in vitro by MTT method. The results indicated that all of these compounds had potent anti-proliferative activity which were more potent than their parent compound and 5-FU, especially 8a-8h and 8j showed the strongest anti-HCC HepG2 cell activity with IC50 values of 0.12-0.93 μmol x L(-1).


Asunto(s)
Humanos , Antineoplásicos , Farmacología , Carcinoma Hepatocelular , Fluorouracilo , Células Hep G2 , Neoplasias Hepáticas , Oxadiazoles , Farmacología
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