Hetarylfuroxans: cytotoxic effect and induction of apoptosis in chronic myeloid leukemia K562 cells


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Hetarylfuroxans (4-(2-methylpyridin-5-yloxy)-3-phenylfuroxan (1), bis(1,2,4-oxadiazol- 3-yl)furoxan (2), and 4-amino-3-(indenotriazin-3-yl)furoxan (3)) exhibit in vitro cytotoxic activity against chronic myeloid leukemia K562 cells. All studied furoxans induce apoptosis in K562 cells. The experiments with activation of caspases-3 and -7 showed that furoxan 3 possessed the highest apoptosis-inducing capacity. The studied hetarylfuroxans were found to be the promising drug candidates for the treatment of chronic myeloid leukemia K562.

作者简介

S. Pukhov

Institute of Physiologically Active Compounds, Russian Academy of Sciences

Email: mnn@ioc.ac.ru
俄罗斯联邦, 1 Severnyi proezd, Chernogolovka, Moscow Region, 142432

L. Anikina

Institute of Physiologically Active Compounds, Russian Academy of Sciences

Email: mnn@ioc.ac.ru
俄罗斯联邦, 1 Severnyi proezd, Chernogolovka, Moscow Region, 142432

A. Larin

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: mnn@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

L. Fershtat

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: mnn@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

A. Kulikov

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: mnn@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

N. Makhova

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

编辑信件的主要联系方式.
Email: mnn@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

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