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新型氨肽酶 N(APN/CD13)抑制剂来源于氯霉素胺。

Novel aminopeptidase N (APN/CD13) inhibitors derived from chloramphenicol amine.

机构信息

Department of Medicinal Chemistry, School of Pharmacy, Shandong University, Ji'nan, Shandong, PR China.

出版信息

Bioorg Med Chem. 2011 Sep 1;19(17):5190-8. doi: 10.1016/j.bmc.2011.07.008. Epub 2011 Jul 14.

Abstract

Aminopeptidase N (APN) is involved in different physiological and pathological processes of tumor cells, including proliferation, invasion, apoptosis and metastasis. Herein one series of compounds derived from commercially available (1S,2S)-2-amino-1-(4-nitrophenyl) propane-1,3-diol have been designed and synthesized. Furthermore, preliminary activity evaluation showed that some compounds elicited moderate inhibitory activity against APN with compounds 10e (IC(50)=6.1±0.5 μM) possessing the best efficacy, which could be used as the lead compound in the future for anticancer agents research.

摘要

氨基肽酶 N(APN)参与肿瘤细胞的不同生理和病理过程,包括增殖、侵袭、凋亡和转移。在此,我们设计并合成了一系列来源于市售的(1S,2S)-2-氨基-1-(4-硝基苯基)丙烷-1,3-二醇的化合物。此外,初步的活性评价表明,一些化合物对 APN 表现出中等抑制活性,其中化合物 10e(IC50=6.1±0.5 μM)的效果最好,它可以作为未来抗癌药物研究的先导化合物。

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