Synthesis and Biological Evaluation of 3-Chloro-4-(indol-3-yl)-2,5- pyrroledione Derivatives as Antitumor Agents

Author(s): Yuchen Lin, Jing Chen

Journal Name: Letters in Drug Design & Discovery

Volume 10 , Issue 5 , 2013

Become EABM
Become Reviewer


A series of 3-chloro-4-(indol-3-yl)-2,5-pyrroledione derivatives were synthesized and evaluated for their cytotoxic activities in vitro against five human cancer cell lines (K562, A549, ECA-109, KB and SMMC-7721). Most compounds displayed potent cytotoxicity with IC50 values in low micromolar range. The results showed that the existence of the chlorine atom at 3-position on the pyrroledione ring was crucial for the activity. Compound 6a, the most potent one (IC50: 0.67∼3.93 μM), would be a promising template for further development of novel antitumor agents

Keywords: Antitumor, 3-Chloro-4-(indol-3-yl)-2, 5-pyrroledione, Cytotoxic activity, Heterocycles, Structure-activity relationship, Synthesis

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2013
Page: [382 - 389]
Pages: 8
DOI: 10.2174/1570180811310050003
Price: $65

Article Metrics

PDF: 16