作者
Kimberly O. Cameron,Daniel W. Kung,Amit S. Kalgutkar,Ravi G. Kurumbail,Russell Miller,Christopher T. Salatto,Jessica L. Ward,Jane M. Withka,Samit K. Bhattacharya,Markus Boehm,Kris A. Borzilleri,Janice A. Brown,Matthew F. Calabrese,Nicole Caspers,Emily Cokorinos,Edward L. Conn,Matthew Dowling,David J. Edmonds,Heather Eng,Dilinie P. Fernando,Richard K. Frisbie,David Hepworth,James A. Landro,Yuxia Mao,Francis Rajamohan,Allan R. Reyes,Colin R. Rose,Tim Ryder,Andre Shavnya,Aaron Smith,Meihua Tu,Angela Wolford,Jun Xiao
摘要
Adenosine monophosphate-activated protein kinase (AMPK) is a protein kinase involved in maintaining energy homeostasis within cells. On the basis of human genetic association data, AMPK activators were pursued for the treatment of diabetic nephropathy. Identification of an indazole amide high throughput screening (HTS) hit followed by truncation to its minimal pharmacophore provided an indazole acid lead compound. Optimization of the core and aryl appendage improved oral absorption and culminated in the identification of indole acid, PF-06409577 (7). Compound 7 was advanced to first-in-human trials for the treatment of diabetic nephropathy.