A Comparative Study of Antitumor Activities and DNA Cleavage On A Class of Dehydroabietylamine Derivatives
Document Type
Article
Publication Date
11-1-2013
Publication Title
Pharmazie
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 for fourteen 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.
Recommended Citation
Liu, Chao Xiang; Lin, Zhong Xiang; Yu, Xing; Lu, Zhou; Zhou, Aimin; and Bao, Yong Li, "A Comparative Study of Antitumor Activities and DNA Cleavage On A Class of Dehydroabietylamine Derivatives" (2013). Chemistry Faculty Publications. 423.
https://engagedscholarship.csuohio.edu/scichem_facpub/423
DOI
10.1691/ph.2013.3575
Volume
68
Issue
11