Identification and Validation of an inhibitor of the protein kinases PIM and DYRK
Gyula Bencze, Prabhadevi VenkataramaniiD, Elad ElkayamiD, Keith D. RiveraiD, Ankur GargiD, Istvan Szabadakai, László ŐrfiiD, Leemor Joshua‐ToriD, Darryl PappiniD, Nicholas K. TonksiD
Abstract
Fermented wheat germ extract (FWGE), a nutraceutical with reported anticancer properties, contains numerous biologically active molecules, but its precise therapeutic constituents remain unclear. In this study, we identify and characterize a novel small-molecule inhibitor, CSH-4044, isolated from FWGE. Through preparative HPLC and structural elucidation via X-ray crystallography, CSH-4044 was revealed to be a unique benzothiazole compound. Kinase profiling demonstrated its high specificity toward the PIM and DYRK families of protein kinases. We determined the co-crystal structure of CSH-4044 bound to PIM1, revealing ATP-competitive binding, and critical hydrophobic and hydrogen-bonding interactions. A chemically synthesized version of CSH-4044 mirrored the activity of the natural product, confirming structural integrity and biological equivalence. Functionally, CSH-4044 suppressed PIM3-driven BAD phosphorylation in pancreatic cancer cells and reduced DYRK1A-mediated Tau phosphorylation in neuronal cells. Our findings position CSH-4044 as a promising lead for targeting PIM and DYRK families of kinases and highlight FWGE as a source of potential therapeutic compounds.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 3
- FWCI
- 3.48
- Field percentile
- top 9%
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- PKIS Deep Dive Yields a Chemical Starting Point for Dark Kinases and a Cell Active BRSK2 Inhibitor
T. Y. Tamir, D. H. Drewry, … A. D. Axtman·bioRxiv·Jun 15, 2020
- Novel small-molecule inhibitors of the protein kinase DYRK: Potential Therapeutic candidates in cancer
Prabhadevi Venkataramani, Elad Elkayam, … Nicholas K. Tonks·bioRxiv·Nov 5, 2025
- The off-target kinase landscape of clinical PARP inhibitors
A. A. Antolin, M. Ameratunga, … B. Al-Lazikani·bioRxiv·Jan 14, 2019
- Targeting the PI5P4K lipid kinase family in cancer using novel covalent inhibitors
S. C. Sivakumaren, H. Shim, … N. S. Gray·bioRxiv·Oct 25, 2019
- An open source plant kinase chemogenomics set
M. F. Ercoli, P. Zonzini Ramos, … P. C. Ronald·bioRxiv·Jun 18, 2022
- Identification and Optimization of cell active 4-anilino-quin(az)oline Inhibitors for Protein Kinase Novel 3 (PKN3)
C. R. M. Asquith, L. Temme, … D. H. Drewry·bioRxiv·Mar 2, 2020