Vincent J. Colandrea, Amruta Joshi-Pangu, Robert T. Nolte, R. Bledsoe, Paris Ward, Jack Glancy, Matthew Kowalski, Chelsea A. Huff, Sapna Desai, R. Nagilla, N. Laping, J. Axten, K. Evans
2026.1.15ACS Medicinal Chemistry Letters
tlooto Summary
The first high resolution X-ray cocrystal structure of the eIF2B (α,β,δ)2 complex with compound 7a is reported, which can inform subsequent SAR.
Abstract
ISRIB reactivates protein synthesis for cells under stress through the stabilization of eukaryotic initiation factor 2 beta (eIF2B). We discovered that diaminoisohexides, derived from isomannide and isosorbide serve as a bioisostere for the diamino cyclohexane core in ISRIB. These scaffolds conferred improved solubility but also showed activity for the human ether-a-go-go-related gene (hERG). Herein we describe our efforts to mitigate hERG activity while maintaining target potency. The first high resolution (2.25Å) X-ray cocrystal structure of the eIF2B (α,β,δ)2 complex with compound 7a is reported, which can inform subsequent SAR.
Citation format
COLANDREA, Vincent J., et al. Discovery of isohexide bisglycolamides as inhibitors of the integrated stress response. ACS Medicinal Chemistry Letters, 2026, 17 2(2): 495–502.