前药
化学
活性氧
过氧化氢
癌细胞
DNA
氮芥
选择性
生物化学
组合化学
癌症
药理学
化疗
催化作用
内科学
外科
医学
环磷酰胺
作者
Yunyan Kuang,Kumudha Balakrishnan,Varsha V. Gandhi,Xiaohua Peng
摘要
The major concern for anticancer chemotherapeutic agents is the host toxicity. The development of anticancer prodrugs targeting the unique biochemical alterations in cancer cells is an attractive approach to achieve therapeutic activity and selectivity. We designed and synthesized a new type of nitrogen mustard prodrug that can be activated by high level of reactive oxygen species (ROS) found in cancer cells to release the active chemotherapy agent. The activation mechanism was determined by NMR analysis. The activity and selectivity of these prodrugs toward ROS was determined by measuring DNA interstrand cross-links and/or DNA alkylations. These compounds showed 60-90% inhibition toward various cancer cells, while normal lymphocytes were not affected. To the best of our knowledge, this is the first example of H(2)O(2)-activated anticancer prodrugs.
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