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1.
Journal of International Pharmaceutical Research ; (6): 680-685, 2014.
Artigo em Chinês | WPRIM | ID: wpr-845822

RESUMO

Objective: To design and synthesize conjugates of alkoxylbiphenyl/C5-curcumine with antitumor activities. Methods: Bicyclol, acetone and benzaldehyde with various substituents were used as raw materials. The target compounds were obtained by oxidizing and Aldol condensation reaction. And their antitumor activities were evaluated by MTS assay in the parental sensitive K562 and drug-resistant K562/A02 cell lines. Results: Twelve alkoxylbiphenyl/C5-curcumine conjugates were prepared.

2.
Journal of International Pharmaceutical Research ; (6): 680-685, 2014.
Artigo em Chinês | WPRIM | ID: wpr-457399

RESUMO

Objecti ve To design and synthesize conjugates of alkoxylbiphenyl/C5-curcumine with antitumor activities. Methods Bicyclol,acetone and benzaldehyde with various substituents were used as raw materials. The target compounds were obtained by oxidizing and Aldol condensation reaction. And their antitumor activities were evaluated by MTS assay in the parental sensitive K562 and drug-resistant K562/A02 cell lines. Results Twelve alkoxylbiphenyl/C5-curcumine conjugates were prepared. Conclusion The synthetic procedure of the target compounds is simple,and the yield is high. Compound 3b could significantly inhibit K562 and drug-resistant K562/A02 cell proliferation,and the IC50 is 5.38 and 3.60μmol/L,respectively.

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