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Journal of Medicinal Chemistry|November 20, 2020
A Chemical Probe for Dark Kinase STK17B Derives Its Potency and High Selectivity through a Unique P-Loop ConformationAlfredo Picado, Apirat Chaikuad, Carrow I Wells, et al.
Biorxiv : the Preprint Server for Biology|May 27, 2024
Discovery and Characterization of a Chemical Probe for Cyclin-Dependent Kinase-Like 2Frances M Bashore, Sophia M Min, Xiangrong Chen, et al.
Chemmedchem|October 27, 2017
Identification and Optimization of 4-Anilinoquinolines as Inhibitors of Cyclin G Associated KinaseChristopher R M Asquith, Tuomo Laitinen, James M Bennett, et al.
ACS Medicinal Chemistry Letters|August 14, 2024
Discovery and Characterization of a Chemical Probe for Cyclin-Dependent Kinase-Like 2Frances M Bashore, Sophia M Min, Xiangrong Chen, et al.
Nature Communications|February 14, 2025
Structural insights into human brachyury DNA recognition and discovery of progressible binders for cancer therapyJoseph A Newman, Angeline E Gavard, Nergis Imprachim, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 27, 2021
Non-canonical role of Hippo tumor suppressor serine/threonine kinase 3 STK3 in prostate cancerAmelia U Schirmer, Lucy M Driver, Megan T Zhao, et al.
Biorxiv : the Preprint Server for Biology|February 17, 2023
A Potent and Selective CDKL5/GSK3 Chemical Probe is NeuroprotectiveHan Wee Ong, Yi Liang, William Richardson, et al.
ACS Chemical Neuroscience|April 21, 2023
Discovery of a Potent and Selective CDKL5/GSK3 Chemical Probe That Is NeuroprotectiveHan Wee Ong, Yi Liang, William Richardson, et al.
Scientific Reports|November 13, 2019
Binding and structural analyses of potent inhibitors of the human Ca2+/calmodulin dependent protein kinase kinase 2 (CAMKK2) identified from a collection of commercially-available kinase inhibitorsGerson S Profeta, Caio V Dos Reis, André da S Santiago, et al.
Current Research in Chemical Biology|November 27, 2023
SGC-CLK-1: A chemical probe for the Cdc2-like kinases CLK1, CLK2, and CLK4Deanna Tiek, Carrow I Wells, Martin Schröder, et al.
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