1239591-13-9Relevant academic research and scientific papers
Synthesis and molecular docking studies of novel 2-chloro-pyridine derivatives containing flavone moieties as potential antitumor agents
Liu, Xin-Hua,Liu, Hui-Feng,Shen, Xu,Song, Bao-An,Bhadury, Pinaki S.,Zhu, Hai-Liang,Liu, Jin-Xing,Qi, Xing-Bao
scheme or table, p. 4163 - 4167 (2010/08/20)
A series of novel 2-chloro-pyridine derivatives containing flavone, chrome or dihydropyrazole moieties as potential telomerase inhibitors were synthesized. The bioassay tests showed that compounds 6e and 6f exhibited some effect against gastric cancer cell SGC-7901 with IC50 values of 22.28 ± 6.26 and 18.45 ± 2.79 μg/mL, respectively. All title compounds were assayed for telomerase inhibition by a modified TRAP assay, the results showed that compound 6e can strongly inhibit telomerase with IC50 value of 0.8 ± 0.07 μM. Docking simulation was performed to position compound 6e into the active site of telomerase (3DU6) to determine the probable binding model.
