Synthesis, anticancer, structural, and computational docking studies of 3-benzylchroman-4-one derivatives
作者:Lalitha Simon、Abdul Ajees Abdul Salam、S. Madan Kumar、T. Shilpa、K.K. Srinivasan、K. Byrappa
DOI:10.1016/j.bmcl.2017.10.026
日期:2017.12
exhibited moderate activity against HeLa cells (IC50 = 42.8 µM). The molecular structures of 3h and 3i were solved by single crystal X-ray crystallographic technique. Additionally, the molecular docking studies between the tumour suppressor protein p53 with the lead compound 3h, which exhibited better anticancer activity against HeLa cells was examined.