Discovery of First Branched-Chain Ketoacid Dehydrogenase Kinase (BDK) Inhibitor Clinical Candidate PF-07328948

Inhibition of branched-chain ketoacid dehydrogenase kinase (BDK or BCKDK), a negative regulator of branched-chain amino acid (BCAA) metabolism, is hypothesized to treat cardio-metabolic diseases. From a starting point with potential idiosyncratic toxicity risk, modification to a benzothiophene core and discovery of a cryptic pocket allowed for improved potency with 3-aryl substitution to arrive at PF-07328948, which was largely devoid of protein covalent binding liability. This BDK inhibitor was shown also to be a BDK degrader in cells and in vivo rodent studies. Plasma biomarkers, including BCAAs and branched-chain ketoacids (BCKAs), were lowered in vivo with enhanced pharmacodynamic effect upon chronic dosing due to BDK degradation. This molecule improves metabolic and heart failure end points in rodent models. PF-07328948 is the first known selective BDK inhibitor candidate to be examined in clinical studies, with Phase 1 single ascending dose data showing good tolerability and a pharmacokinetic profile commensurate with once-daily dosing.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2024-11-19
DOI
https://doi.org/10.1021/acs.jmedchem.4c02230
Citations
10
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
2.34
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article

Discovery of First Branched-Chain Ketoacid Dehydrogenase Kinase (BDK) Inhibitor Clinical Candidate PF-07328948

James Bradow, Shenping Liu, Rachel J. Roth Flach, George Williams et al.
10 citations
Journal of Medicinal Chemistry
Protein Structure and Dynamics
2.34
article

Discovery of First Branched-Chain Ketoacid Dehydrogenase Kinase (BDK) Inhibitor Clinical Candidate PF-07328948

James Bradow, Shenping Liu, Rachel J. Roth Flach, George Williams, Andrew J. Bessire, Karen J. Coffman, John D. Groarke, Spinel Karas, Luis Martinez-Alsina, Leanne M. Buzon, Amanda Balesano, Ruolun Qiu, Bethany L. Kormos, Amy Rosado, Parag V. Sahasrabudhe, Kevin J. Filipski, John D. Knafels, Christine C. Orozco, William P. Esler, Matthew A. Cerny, Eliza Bollinger, Dinesh Hirenallur‐Shanthappa, Mackenzie Marshall, Kimberly O. Cameron, Brigitte Laforest, Edelweiss Evrard, Matthew R. Reese, Allan R. Reyes, Kay Neale, Amit S.S. Kalgutkar, John C. Stansfield, Jie Chen, Xian Chen, Yuan Zhang
article en
10 citations

Abstract

Inhibition of branched-chain ketoacid dehydrogenase kinase (BDK or BCKDK), a negative regulator of branched-chain amino acid (BCAA) metabolism, is hypothesized to treat cardio-metabolic diseases. From a starting point with potential idiosyncratic toxicity risk, modification to a benzothiophene core and discovery of a cryptic pocket allowed for improved potency with 3-aryl substitution to arrive at PF-07328948, which was largely devoid of protein covalent binding liability. This BDK inhibitor was shown also to be a BDK degrader in cells and in vivo rodent studies. Plasma biomarkers, including BCAAs and branched-chain ketoacids (BCKAs), were lowered in vivo with enhanced pharmacodynamic effect upon chronic dosing due to BDK degradation. This molecule improves metabolic and heart failure end points in rodent models. PF-07328948 is the first known selective BDK inhibitor candidate to be examined in clinical studies, with Phase 1 single ascending dose data showing good tolerability and a pharmacokinetic profile commensurate with once-daily dosing.

Journal of Medicinal ChemistryVol. 68(3)
Pfizer (United States) (US)
Openalex Percentile: Top 11%
Protein Structure and Dynamics
2.34
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