| Literature DB >> 24794770 |
Jing Wu1, Linxi Yu1, Feifei Yang1, Jingjie Li1, Peng Wang1, Wenbo Zhou1, Liwen Qin1, Yunqi Li1, Jian Luo1, Zhengfang Yi2, Mingyao Liu3, Yihua Chen4.
Abstract
A series of 2,3-diaryl-4-thiazolidinone derivatives were synthesized and evaluated for their antiproliferative properties against two well-known cancer cell lines (A549 as human lung cancer and MDA-MB-231 as human breast cancer). Structure activity relationship (SAR) analysis resulted in the discovery of 2-(3-(arylalkyl amino carbonyl)phenyl)-3-(2-methoxy-phenyl)-4-thiazolidinone derivatives with high potent inhibitory effects on the proliferation of both cancer cell lines. Furthermore, several compounds with potent antiproliferative activities displayed excellent inhibitory activities on migration with an IC50 of about 0.05 μM on MDA-MB-231 cells in two different migration assays. In particular, compound 39 was indicated to suppress tumor growth and metastasis as well as promote survival rate. Intriguingly, this series of analogs have been indicated to inhibit tumor cell proliferation through inducing cell cycle arrest. These results suggested that the new series of 2-(3-(arylalkyl amino carbonyl)phenyl)-3-(2-methoxyphenyl)-4-thiazolidinone derivatives could be regarded and developed as novel highly potential anticancer agents in the future.Entities:
Keywords: Antitumor growth and metastasis; Structure–activity relationships; Thiazolidinone derivatives
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Year: 2014 PMID: 24794770 DOI: 10.1016/j.ejmech.2014.04.068
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514