| Literature DB >> 26896708 |
Yue-Qing Li1, Fei Yang1, Liu Wang1, Zhi Cao1, Tian-Jiao Han1, Zhe-Ang Duan1, Zhen Li1, Wei-Jie Zhao2.
Abstract
A series of flavone-7-phosphoramidate derivatives were synthesized and tested for their antiproliferative activity in vitro against human hepatoma cell line HepG2 and human normal hepatic cell line L-O2. Compound 8d, 16d and 17d, incorporating the amino acid alanine, exhibited high inhibitory activity on HepG2 cell line with IC50 values of 9.0 μmol/L, 5.5 μmol/L and 6.6 μmol/L. The introduction of acyl groups played a pivotal role in the selective inhibition toward human hepatoma HepG2 cells, except for compound 8a, 9a and 16b. Compound 8d, 16d and 17d could significantly induce G2/M arrest in HepG2 cells. Specially, Compound 16d could lead early apoptosis in HepG2 cells.Entities:
Keywords: Apoptosis; Flavone; G2/M arrest; HepG2; Phosphoramidate
Mesh:
Substances:
Year: 2016 PMID: 26896708 DOI: 10.1016/j.ejmech.2016.02.012
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514