| Literature DB >> 26384290 |
Chao Zhang1, Shasha Li1, Liyan Ji1, Shan Liu1, Zhongjun Li1, Shuchun Li1, Xiangbao Meng2.
Abstract
Three groups of non-camptothecin compounds with four to five fused rings have been designed and synthesized. Their in vitro anti-proliferative activity has been evaluated with five different cancer cell lines (HCT116, PC3, U87MG, HepG2, SK-OV-3). Compounds B-2 and B-3 showed the most potent cell growth inhibition with IC50 of 169 nM and 325 nM against U87MG cell line correspondingly.Entities:
Keywords: Anti-cancer; Inhibitor; Synthesis; Topo I
Mesh:
Substances:
Year: 2015 PMID: 26384290 DOI: 10.1016/j.bmcl.2015.06.042
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823