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Unexpected Noncovalent Off-Target Activity of Clinical BTK Inhibitors Leads to Discovery of a Dual NUDT5/14 Antagonist

Balıkçı E. et al, (2024), Journal of Medicinal Chemistry, 67, 7245 - 7259

Imidazo[1,2-b]pyridazines as inhibitors of DYRK kinases.

Henderson SH. et al, (2024), European journal of medicinal chemistry, 269

Recent advances in the structural biology of tyrosine kinases.

Rygiel KA. and Elkins JM., (2023), Current opinion in structural biology, 82

Target 2035 – an update on private sector contributions

Ackloo S. et al, (2023), RSC Medicinal Chemistry, 14, 1002 - 1011

An open source plant kinase chemogenomics set.

Ercoli MF. et al, (2022), Plant direct, 6

Development of dihydropyrrolopyridinone-based PKN2/PRK2 chemical tools to enable drug discovery.

Scott F. et al, (2022), Bioorganic & medicinal chemistry letters, 60

Chemical Probes for Understudied Kinases: Challenges and Opportunities.

Serafim RAM. et al, (2021), Journal of medicinal chemistry

Discovery of a Potent Dual SLK/STK10 Inhibitor Based on a Maleimide Scaffold.

Serafim RAM. et al, (2021), Journal of medicinal chemistry

Discovery and Characterization of Selective and Ligand-Efficient DYRK Inhibitors.

Henderson SH. et al, (2021), Journal of medicinal chemistry, 64, 11709 - 11728

Structure-kinetic relationship reveals the mechanism of selectivity of FAK inhibitors over PYK2.

Berger B-T. et al, (2021), Cell chemical biology, 28, 686 - 698.e7

Aminothiazolones as potent, selective and cell active inhibitors of the PIM kinase family.

Quevedo CE. et al, (2020), Bioorganic & medicinal chemistry, 28

Mining Public Domain Data to Develop Selective DYRK1A Inhibitors.

Henderson SH. et al, (2020), ACS medicinal chemistry letters, 11, 1620 - 1626

Development of 2-(4-pyridyl)-benzimidazoles as PKN2 chemical tools to probe cancer.

Scott F. et al, (2020), Bioorganic & medicinal chemistry letters, 30

SGC-AAK1-1: A Chemical Probe Targeting AAK1 and BMP2K.

Wells C. et al, (2020), ACS medicinal chemistry letters, 11, 340 - 345

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