8, 9-methylenedioxybenzo [i] phenanthridines: topoisomerase I-targeting activity and cytotoxicity
D Li, B Zhao, SP Sim, TK Li, A Liu, LF Liu…
Index: Li, Dajie; Zhao, Baoping; Sim, Sai-Peng; Li, Tsai-Kun; Liu, Angela; Liu, Leroy F.; LaVoie, Edmond J. Bioorganic and Medicinal Chemistry, 2003 , vol. 11, # 17 p. 3795 - 3805
Full Text: HTML
Citation Number: 35
Abstract
Substituted benzo [i] phenanthridines that have incorporated within their structure an 8, 9- methylenedioxy group can exhibit topoisomerase I-targeting activity. Structure–activity studies were performed to examine the influence of saturation at the 11, 12-positions of several substituted 8, 9-methylenedioxybenzo [i] phenanthridines. The activities of these dihydro analogues were compared to those of their unsaturated analogues. In addition, ...
Related Articles:
Biorenewable polyethylene terephthalate mimics derived from lignin and acetic acid
[Mialon, Laurent; Pemba, Alexander G.; Miller, Stephen A. Green Chemistry, 2010 , vol. 12, # 10 p. 1704 - 1706]
Conversion of dehydrodiferulic acids by human intestinal microbiota
[Journal of Agricultural and Food Chemistry, , vol. 57, # 8 p. 3356 - 3362]
Conversion of dehydrodiferulic acids by human intestinal microbiota
[Journal of Agricultural and Food Chemistry, , vol. 57, # 8 p. 3356 - 3362]