Role of Epoxide Hydrolases and Cytochrome P450s on Metabolism of KZR-616, a First-in-Class Selective Inhibitor of the Immunoproteasome

• Published in: Drug metabolism and disposition 2021-09, Vol.49 (9), p.810-821
• Main Authors: Fang, Ying, Johnson, Henry, Anderl, Janet L., Muchamuel, Tony, McMinn, Dustin, Morisseau, Christophe, Hammock, Bruce D., Kirk, Christopher, Wang, Jinhai
• Format: Article
• Language: English
• Subjects: Animals; Autoimmune Diseases - drug therapy; Cells, Cultured; Cysteine Endopeptidases - immunology; Cysteine Endopeptidases - metabolism; Cytochrome P-450 Enzyme System - metabolism; Epoxide Hydrolases - immunology; Epoxide Hydrolases - metabolism; Hepatocytes - metabolism; Humans; Inactivation, Metabolic; Inflammation - drug therapy; Macaca fascicularis; Morpholines - pharmacology; Proteasome Endopeptidase Complex - immunology; Proteasome Inhibitors - pharmacology; Proteins - immunology
• ISSN: 0090-9556; 1521-009X
• DOI: 10.1124/dmd.120.000307

KZR-616 is an irreversible tripeptide epoxyketone-based selective inhibitor of the human immunoproteasome. Inhibition of the immunoproteasome results in anti-inflammatory activity in vitro and based on promising therapeutic activity in animal models of rheumatoid arthritis and systemic lupus erythematosus KZR-616 is being developed for potential treatment of multiple autoimmune and inflammatory diseases. The presence of a ketoepoxide pharmacophore presents unique challenges in the study of drug metabolism during lead optimization and clinical candidate profiling. This study presents a thorough and systematic in vitro and cell-based enzymatic metabolism and kinetic investigation to identify the major enzymes involved in the metabolism and elimination of KZR-616. Upon exposure to liver microsomes in the absence of NADPH, KZR-616 and its analogs were converted to their inactive diol derivatives with varying degrees of stability. Diol formation was also shown to be the major metabolite in pharmacokinetic studies in monkeys and correlated with in vitro stability results for individual compounds. Further study in intact hepatocytes revealed that KZR-616 metabolism was sensitive to an inhibitor of microsomal epoxide hydrolase (mEH) but not inhibitors of cytochrome P450 (P450) or soluble epoxide hydrolase (sEH). Primary human hepatocytes were determined to be the most robust source of mEH activity for study in vitro. These findings also suggest that the exposure of KZR-616 in vivo is unlikely to be affected by coadministration of inhibitors or inducers of P450 and sEH. This work presents a thorough and systematic investigation of metabolism and kinetics of KZR-616 and related analogs in in vitro and cell-based enzymatic systems. Information gained could be useful in assessing novel covalent proteasome inhibitors during lead compound optimization. These studies also demonstrate a robust source in vitro test system that correlated with in vivo pharmacokinetics for KZR-616 and two additional tripeptide epoxyketones.