Structure-activity relationship study of central pyridine-derived TYK2 JH2 inhibitors: Optimization of the PK profile through C4' and C6 variations.

Bioorganic & medicinal chemistry letters 2023 Jul 15

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Efforts directed at improving potency and preparing structurally different TYK2 JH2 inhibitors from the first generation of compounds such as 1a led to the SAR study of new central pyridyl based analogs 2-4. The current SAR study resulted in the identification of 4h as a potent and selective TYK2 JH2 inhibitor with distinct structural differences from 1a. In this manuscript, the in vitro and in vivo profiles of 4h are described. The hWB IC50 of 4h was shown as 41 nM with 94% bioavailability in the mouse PK study. Copyright © 2023 Elsevier Ltd. All rights reserved.

Citation

Zili Xiao, Michael G Yang, Chunjian Liu, Trevor Sherwood, John L Gilmore, James Lin, Peng Li, Dauh-Rurng Wu, John Tokarski, Sha Li, Lihong Cheng, Chunshan Xie, Jingsong Fan, Elizabeth Dierks, Joann Strnad, Mary Ellen Cvijic, Javed Khan, Max Ruzanov, Michael Galella, Purnima Khandelwal, Alaric J Dyckman, Arvind Mathur, Louis J Lombardo, John E Macor, Percy H Carter, Nelly Aranibar, James R Burke, David S Weinstein. Structure-activity relationship study of central pyridine-derived TYK2 JH2 inhibitors: Optimization of the PK profile through C4' and C6 variations. Bioorganic & medicinal chemistry letters. 2023 Jul 15;91:129373