Natural Science Laboratory, Division of Medicinal and Pharmaceutical Chemistry, Department of Pharmaceutical Technology , Jadavpur University , P.O. Box 17020, Kolkata 700032 , West Bengal , India.
J Med Chem. 2018 Aug 9;61(15):6468-6490. doi: 10.1021/acs.jmedchem.7b00782. Epub 2018 Apr 16.
Aminopeptidase N (APN) is an important metalloenzyme. It regulates multivariate cellular functions by different mechanisms such as enzymatic cleavage of peptides. This may play a role in endocytosis and regulate signal transduction. APN, a member of the M1 zinc metallopeptidase family, plays crucial roles in a variety of functions such as migration and invasion, and angiogenesis and metastasis of tumor cells. Therefore, APN inhibitors may be useful for the treatment of cancer. In this Perspective, structure-activity relationships of APN inhibitors are discussed to get an idea of possible lead candidates. APN inhibitors should possess an aryl hydrophobic function along with a zinc binding group attached to the hydrophobic group(s) to achieve high potency. This and other design aspects of APN inhibitors are discussed in this Perspective.
氨基肽酶 N(APN)是一种重要的金属酶。它通过不同的机制,如酶切肽,调节多种细胞功能。这可能在胞吞作用中发挥作用,并调节信号转导。APN 是 M1 锌金属肽酶家族的成员,在肿瘤细胞的迁移和侵袭、血管生成和转移等多种功能中发挥着关键作用。因此,APN 抑制剂可能对癌症的治疗有用。在这篇观点文章中,讨论了 APN 抑制剂的构效关系,以了解可能的先导候选物。APN 抑制剂应该具有芳基疏水性功能,以及与疏水分子(s)相连的锌结合基团,以达到高活性。本文讨论了 APN 抑制剂的这一和其他设计方面。