Synthesis of 2-styrylchromones as a novel class of antiproliferative agents targeting carcinoma cells

Arthur Y. Shaw, Chun Yi Chang, Hao Han Liau, Pei Jung Lu, Hui Ling Chen, Chia Ning Yang, Hao Yi Li

研究成果: Article同行評審

62 引文 斯高帕斯(Scopus)

摘要

A series of 2-styrylchromone analogs were synthesized and examined for their antiproliferative effects on a panel of carcinoma cells. Among the tested agents, only 4m exhibited a moderate activity with an IC50 value of 28.9 μM against PC-3 cells which indicates the selectivity of PC-3 cells in response to 2-styrylchromones. In addition, 4q demonstrated the most antiproliferative effect with an IC50 value of 4.9 μM against HeLa cells. Flow cytometric analysis and DAPI staining revealed that HeLa cells exposed to 4q as low as 5 μM induced cell death through sub-G1 arrest and DNA fragmentation. Furthermore, CoMFA analysis of tested 2-styrylchromones resulted in a q2 of 0.459 to generate a 3D-QSAR model on BT483 cell line. Together, these results suggest a potential structural optimization and pharmacological study of 2-styrylchromones.

原文English
頁(從 - 到)2552-2562
頁數11
期刊European Journal of Medicinal Chemistry
44
發行號6
DOIs
出版狀態Published - 2009 六月

All Science Journal Classification (ASJC) codes

  • 藥理
  • 藥物發現
  • 有機化學

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