Synthesis of new xanthone analogues and their biological activity test - Cytotoxicity, topoisomerase II inhibition, and DNA cross-linking study

被引:83
作者
Woo, Sangwook
Jung, Ji
Lee, Chongsoon
Kwon, Youngjoo [1 ]
Na, Younghwa
机构
[1] Ewha Womans Univ, Coll Pharm, Seoul 120750, South Korea
[2] Catholic Univ Daegu, Coll Pharm, Gyongsan 712702, Gyeongbuk, South Korea
[3] Yeungnam Univ, Coll Nat Sci, Dept Biochem, Kyongsan 712749, South Korea
关键词
xanthones; topoisomerase II inhibition; DNA cross-linking; anti-cancer agents;
D O I
10.1016/j.bmcl.2006.12.030
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this report, we prepared some 3-(2',3'-epoxypropoxy)xanthones and their epoxide ring opened halohydrin analogues, and evaluated their cytotoxicity and topoisomerase II inhibition activity using doxorubicin and etoposide as references, respectively. Another xanthone compound 9, 1,3-di(2,3'-epoxypropoxy)xanthone, was also synthesized and its DNA cross-linking property including other two biological activities investigated. The biological test results showed compound 9 possessed excellent cytotoxic and topoisomerase II inhibitory activity than other compounds tested. It also exhibited significant DNA cross-linking activities. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1163 / 1166
页数:4
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