Selection of evodiamine as a novel topoisomerase I inhibitor by structure-based virtual screening and hit optimization of evodiamine derivatives as antitumor agents

G Dong, C Sheng, S Wang, Z Miao, J Yao… - Journal of medicinal …, 2010 - ACS Publications
Human topoisomerase I (TopoI) is recognized as a valuable target for the development of
effective antitumor agents. Structure-based virtual screening was applied to the discovery of …

Selection of evodiamine as a novel topoisomerase I inhibitor by structure-based virtual screening and hit optimization of evodiamine derivatives as antitumor agents

G Dong, C Sheng, S Wang, Z Miao… - Journal of medicinal …, 2010 - pubmed.ncbi.nlm.nih.gov
Human topoisomerase I (TopoI) is recognized as a valuable target for the development of
effective antitumor agents. Structure-based virtual screening was applied to the discovery of …

Selection of evodiamine as a novel topoisomerase I inhibitor by structure-based virtual screening and hit optimization of evodiamine derivatives as antitumor agents.

G Dong, C Sheng, S Wang, Z Miao, J Yao… - Journal of Medicinal …, 2010 - europepmc.org
Human topoisomerase I (TopoI) is recognized as a valuable target for the development of
effective antitumor agents. Structure-based virtual screening was applied to the discovery of …

[引用][C] Selection of Evodiamine as a Novel Topoisomerase I Inhibitor by Structure-Based Virtual Screening and Hit Optimization of Evodiamine Derivatives as …

G Dong, C Sheng, S Wang, Z Miao, J Yao… - Journal of Medicinal …, 2010 - infona.pl
Selection of Evodiamine as a Novel Topoisomerase I Inhibitor by Structure-Based Virtual
Screening and Hit Optimization of Evodiamine Derivatives as Antitumor Agents × Close The …

[PDF][PDF] Selection of Evodiamine as a Novel Topoisomerase I Inhibitor by Structure-based Virtual Screening and Hit Optimization of Evodiamine Derivatives as …

G Dong, C Sheng, S Wang, Z Miao, J Yao, W Zhang - pstorage-acs-6854636.s3 …
The first step of the study was to evaluate the reliability of various kinds of docking methods
for the prediction of the binding pose of TopoI inhibitors (Figure 1) into the crystal structure of …