Design, synthesis and biological evaluation of the novel trehalose derivatives.
- Author:
Fang FANG
;
Yong CHEN
- Publication Type:Journal Article
- MeSH:
Antineoplastic Agents;
chemical synthesis;
pharmacology;
Cell Adhesion;
Cell Line, Tumor;
drug effects;
Drug Design;
Hep G2 Cells;
drug effects;
Human Umbilical Vein Endothelial Cells;
drug effects;
Humans;
Trehalose;
analogs & derivatives;
chemistry
- From:
Acta Pharmaceutica Sinica
2015;50(6):725-732
- CountryChina
- Language:Chinese
-
Abstract:
Using brartemicin as the leading compound, fifteen novel trehalose derivatives were designed and synthesized, and the structures were determined by 11H NMR, MS and element analysis. Inhibitory effects of the target compounds on the proliferation of A549, HepG2 and HUVEC cells were detectec by MTT assay. The abilities of adhesion, invasion and migration of A549 and HepG2 cells inhibited by the synthesized compounds were evaluated through Matrigel experiment and Transwell assay. The results showed that, the target compounds had no significant cytotoxicity (compared with the control, P>0.05) to A549, HepG2 and HUVEC cells at the dose range of 1-32 µmol.L-1. At the above dose range, the inhibitory effects of A549 cells adhesion, invasion and migration and HepG2 cells adhesion and invasion by compounds 79 and 82 are better than brartemicin.
