Design and Synthesis of Clinical Candidate PF-06751979: A Potent, Brain Penetrant, β-Site Amyloid Precursor Protein Cleaving Enzyme 1 (BACE1) Inhibitor Lacking Hypopigmentation
Brian T. O’Neill(Pfizer (United States)), Michael A. Brodney(Vertex Pharmaceuticals (United States)), Gabriela Barreiro(Pfizer (United States)), Cathleen Gonzales, Claire M. Steppan(University of Pittsburgh), David Riddell(Eli Lilly (United States)), Kimberly Lapham(Scripps Research Institute), Erik LaChapelle(Pfizer (United States)), Luis Martinez-Alsina(Pfizer (United States)), Christopher Houle(Pfizer (United States)), Katherine Hales(Pfizer (United States)), Germaine Boucher(Pfizer (United States)), Leanne M. Buzon(Pfizer (United States)), Kevin Ogilvie(Pfizer (United States)), Xinjun Hou(Pfizer (United States)), Lorraine F. Lanyon(Scripps Research Institute), David A. Karanian(Pfizer (United States)), Charles E. Nolan(Pfizer (United States)), Shawn D. Doran(Pfizer (United States)), Claude Ambroise(Pfizer (United States)), John C. Murray(Pfizer (United States)), Ashley Robshaw(Pfizer (United States)), Cheng Chang(Pfizer (United States)), Lei Zhang(Pfizer (United States)), Christopher R. Butler(Pfizer (United States)), Karamjeet Pandher(Pfizer (United States)), Elizabeth M. Beck(Pfizer (United States)), Anabella Villalobos(Pfizer (United States)), Kelly R. Bales(Eli Lilly (United States)), Bruce N. Rogers(Pfizer (United States)), Jason K. Dutra(Pfizer (United States))
Cited by 42
Related Papers
ApoE Promotes the Proteolytic Degradation of Aβ
|Neuron|2008|869
Immunization reverses memory deficits without reducing brain Aβ burden in Alzheimer's disease model
|Nature Neuroscience|2002|858
Lack of apolipoprotein E dramatically reduces amyloid β-peptide deposition
|Nature Genetics|1997|835
Neuronal sorting protein-related receptor sorLA/LR11 regulates processing of the amyloid precursor protein
|Proceedings of the National Academy of Sciences|2005|659
Application of the Bicyclo[1.1.1]pentane Motif as a Nonclassical Phenyl Ring Bioisostere in the Design of a Potent and Orally Active γ-Secretase Inhibitor
|Journal of Medicinal Chemistry|2012|460