A comparative study of antitumor activities and DNA cleavage on a class of dehydroabietylamine derivatives.

Chaoxiang Liu, Zhongxiang Lin, Xing Yu, Zhou Lu, Ai-min Zhou, Y. Bao
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Abstract

A series of novel dehydroabietylamine derivatives containing tricyclic diterpene structures were synthesized. The antitumor activities of these compounds against L02, Hey-1B and HepG2 cells were investigated. Significant activity was discovered forfourteen analogs. Meanwhile these compounds exhibit DNA cleavage activities on plasmid DNA (Escherichia coli), which depend on the Schiff base structure and the substituent of the aromatic moiety. Our findings present further information on the relationship between the chemical structure, biological function and DNA cleavage characteristics.
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一类脱氢枞胺衍生物的抗肿瘤活性和DNA裂解的比较研究。
合成了一系列具有三环二萜结构的新型脱氢枞胺衍生物。研究了这些化合物对L02、Hey-1B和HepG2细胞的抗肿瘤活性。14个类似物被发现有显著活性。同时,这些化合物在质粒DNA(大肠杆菌)上表现出DNA裂解活性,这取决于希夫碱基结构和芳香部分的取代基。我们的发现进一步揭示了其化学结构、生物学功能与DNA切割特性之间的关系。
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