869527-83-3Relevant academic research and scientific papers
Optimization of Hydroxyethylamine Transition State Isosteres as Aspartic Protease Inhibitors by Exploiting Conformational Preferences
Bueno, Ana B.,Agejas, Javier,Broughton, Howard,Dally, Robert,Durham, Timothy B.,Espinosa, Juan Félix,González, Rosario,Hahn, Patric J.,Marcos, Alicia,Rodríguez, Ramón,Sanz, Gema,Soriano, José F.,Timm, David,Vidal, Paloma,Yang, Hsiu-Chiung,McCarthy, James R.
, p. 9807 - 9820 (2017/12/26)
NMR conformational analysis of a hydroxyethylamine peptide isostere developed as an aspartic protease inhibitor shows that it is a flexible architecture. Cyclization to form pyrrolidines, piperidines, or morpholines results in a preorganization of the who
BACE INHIBITORS
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Page/Page column 53, (2008/06/13)
The present invention provides BACE inhibitors of Formula (I): methods for their use and preparation, and intermediates for their preparation.
