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- W2891201256 abstract "Kallikrein-related peptidase 6 (KLK6) is a secreted serine protease that belongs to the family of tissue kallikreins (KLKs). Many KLKs are investigated as potential biomarkers for cancer as well as therapeutic drug targets for a number of pathologies. KLK6, in particular, has been implicated in neurodegenerative diseases and cancer, but target validation has been hampered by a lack of selective inhibitors. This work introduces a class of depsipeptidic KLK6 inhibitors, discovered via high-throughput screening, which were found to function as substrate mimics that transiently acylate the catalytic serine of KLK6. Detailed structure–activity relationship studies, aided by in silico modeling, uncovered strict structural requirements for potency, stability, and acyl-enzyme complex half-life. An optimized scaffold, DKFZ-251, demonstrated good selectivity for KLK6 compared to other KLKs, and on-target activity in a cellular assay. Moreover, DKFZ-633, an inhibitor-derived activity-based probe, could be used to pull down active endogenous KLK6." @default.
- W2891201256 created "2018-09-27" @default.
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- W2891201256 date "2018-09-13" @default.
- W2891201256 modified "2023-10-17" @default.
- W2891201256 title "Depsipeptides Featuring a Neutral P1 Are Potent Inhibitors of Kallikrein-Related Peptidase 6 with On-Target Cellular Activity" @default.
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- W2891201256 doi "https://doi.org/10.1021/acs.jmedchem.8b01106" @default.
- W2891201256 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30212625" @default.
- W2891201256 hasPublicationYear "2018" @default.
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