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This compound primarily binds to the enzyme’s active site pocket through hydrophobic interactions and hydrogen bond networks but does not form covalent bonds with active site cysteine residues ( Animal pharmacodynamic studies show that HSK31858-treated mice had NSP activity reduced to 15%–40% of controls and demonstrated significant anti-inflammatory activity in rat COPD models, providing important preliminary validation data for clinical application ( 6 Clinical research progress of DPP1 inhibitors 6.1 Clinical studies of brensocatib 6.1.1 Phase I clinical studies 6.1.1.1 Safety and pharmacokinetics in healthy volunteer Phase I clinical studies of brensocatib focused on evaluating drug safety, tolerability, pharmacokinetics, and pharmacodynamic characteristics in healthy subjects

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