Novel indoline-2,3-dione derivatives as inhibitors of aminopeptidase N (APN)

Abstract

Aminopeptidase N (APN/CD13), as a zinc-containing ectoenzyme, plays a critical role in the process of tumor angiogenesis, invasion and metastasis. Through the docking-based virtual screening of chemical databases and the further activity assay, we discovered that compound 10c exhibits potent and selective inhibitory ability towards APN. In addition, a series of indoline-2,3-dione derivates have been designed and synthesized as APN inhibitors. The results of preliminary activity evaluation showed that compound 12a (IC50=0.074±0.0026μM) exhibited the best inhibitory activity against APN, which could be used for further anticancer agent research.