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Bioorganic & Medicinal Chemistry Letters|March 19, 2011
Phenoxyacetic acids as PPARδ partial agonists: synthesis, optimization, and in vivo efficacyKaren A Evans, Barry G Shearer, David D Wisnoski, et al.Nature|February 15, 2002
Structural basis for antagonist-mediated recruitment of nuclear co-repressors by PPARalphaH Eric Xu, Thomas B Stanley, Valerie G Montana, et al.Bioorganic & Medicinal Chemistry Letters|July 30, 2011
Discovery of GSK1997132B a novel centrally penetrant benzimidazole PPARγ partial agonistMairi Sime, Amanda C Allan, Paul Chapman, et al.Journal of Medicinal Chemistry|April 28, 2006
Biarylaniline phenethanolamines as potent and selective beta3 adrenergic receptor agonistsDavid E Uehling, Barry G Shearer, Kelly H Donaldson, et al.Journal of Medicinal Chemistry|August 13, 2015
Discovery of 4-Amino-8-quinoline Carboxamides as Novel, Submicromolar Inhibitors of NAD-Hydrolyzing Enzyme CD38J David Becherer, Eric E Boros, Tiffany Y Carpenter, et al.Journal of Medicinal Chemistry|April 2, 2015
Discovery, Synthesis, and Biological Evaluation of Thiazoloquin(az)olin(on)es as Potent CD38 InhibitorsCurt D Haffner, J David Becherer, Eric E Boros, et al.Bioorganic & Medicinal Chemistry|October 15, 2020
The exploration of aza-quinolines as hematopoietic prostaglandin D synthase (H-PGDS) inhibitors with low brain exposureRodolfo Cadilla, David N Deaton, Young Do, et al.Pageof 2