Discovery of Orally Active Isofuranones as Potent, Selective Inhibitors of Hematopoetic Progenitor Kinase 1
Andrew P. Degnan, Godwin Kumi, Christopher W. Allard, Erika Araujo, Walter L. Johnson, Kurt Zimmermann, Bradley C. Pearce, S. Sheriff, Alan Futran, Xin Li, Gregory Locke, Dan You, J. S. Morrison, Karen E. Parrish, Caitlyn Stromko, Anwar Murtaza, Jinqi Liu, Benjamin M. Johnson, Gregory D. Vite, Mark D. Wittman
Abstract
While the discovery of immune checkpoint inhibitors has led to robust, durable responses in a range of cancers, many patients do not respond to currently available therapeutics. Therefore, an urgent need exists to identify alternative mechanisms to augment the immune-mediated clearance of tumors. Hematopoetic progenitor kinase 1 (HPK1) is a serine-threonine kinase that acts as a negative regulator of T-cell receptor (TCR) signaling, to dampen the immune response. Herein we describe the structure-based discovery of isofuranones as inhibitors of HPK1. Optimization of the chemotype led to improvements in potency, selectivity, plasma protein binding, and metabolic stability, culminating in the identification of compound 24. Oral administration of 24, in combination with an anti-PD1 antibody, demonstrated robust enhancement of anti-PD1 efficacy in a syngeneic tumor model of colorectal cancer.