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Discovery and <i>In Vivo</i> Anti-inflammatory Activity Evaluation of a Novel Non-peptidyl Non-covalent Cathepsin C Inhibitor

Xing Chen, Yaoyao Yan, Zhaoyan Zhang, Faming Zhang, Mingming Liu, Leran Du, Haixia Zhang, Xiaobao Shen, Dahai Zhao, Jing Shi, Xinhua Liu

2021Journal of Medicinal Chemistry22 citationsDOIOpen Access PDF

Abstract

Cathepsin C (Cat C) participates in inflammation and immune regulation by affecting the activation of neutrophil serine proteases (NSPs). Therefore, cathepsin C is an attractive target for treatment of NSP-related inflammatory diseases. Here, the complete discovery process of the first potent “non-peptidyl non-covalent cathepsin C inhibitor” was described with hit finding, structure optimization, and lead discovery. Starting with hit 14, structure-based optimization and structure–activity relationship study were comprehensively carried out, and lead compound 54 was discovered as a potent drug-like cathepsin C inhibitor both in vivo and in vitro. Also, compound 54 (with cathepsin C Enz IC50 = 57.4 nM) exhibited effective anti-inflammatory activity in an animal model of chronic obstructive pulmonary disease. These results confirmed that the non-peptidyl and non-covalent derivative could be used as an effective cathepsin C inhibitor and encouraged us to continue further drug discovery on the basis of this finding.

Topics & Concepts

ChemistryCathepsinDrug discoveryIn vivoCathepsin SProteasesCathepsin CLead compoundSerineIn vitroBiochemistryCathepsin BPharmacologyEnzymeBiologyBiotechnologyProtease and Inhibitor MechanismsNeutrophil, Myeloperoxidase and Oxidative MechanismsS100 Proteins and Annexins
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