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

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 sel...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2013-05, Vol.21 (9), p.2663-2670
Hauptverfasser: Jin, Kang, Zhang, Xiaopan, Ma, Chunhua, Xu, Yingying, Yuan, Yumei, Xu, Wenfang
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Sprache:eng
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Zusammenfassung: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. 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.
ISSN:0968-0896
1464-3391
DOI:10.1016/j.bmc.2012.06.024