1370705-40-0Relevant articles and documents
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
Stepan, Antonia F.,Subramanyam, Chakrapani,Efremov, Ivan V.,Dutra, Jason K.,O'Sullivan, Theresa J.,Dirico, Kenneth J.,McDonald, W. Scott,Won, Annie,Dorff, Peter H.,Nolan, Charles E.,Becker, Stacey L.,Pustilnik, Leslie R.,Riddell, David R.,Kauffman, Gregory W.,Kormos, Bethany L.,Zhang, Liming,Lu, Yasong,Capetta, Steven H.,Green, Michael E.,Karki, Kapil,Sibley, Evelyn,Atchison, Kevin P.,Hallgren, Andrew J.,Oborski, Christine E.,Robshaw, Ashley E.,Sneed, Blossom,O'Donnell, Christopher J.
, p. 3414 - 3424 (2012/06/01)
Replacement of the central, para-substituted fluorophenyl ring in the γ-secretase inhibitor 1 (BMS-708,163) withthe bicyclo[1.1.1]pentane motif led to the discovery of compound 3, an equipotent enzyme inhibitor with significant improvements in passive permeability and aqueous solubility. The modified biopharmaceutical properties of 3 translated into excellent oral absorption characteristics (～4-fold Cmax and AUC values relative to 1) in a mouse model of γ-secretase inhibition. In addition, SAR studies into other fluorophenyl replacements indicate the intrinsic advantages of the bicyclo[1.1.1]pentane moiety over conventional phenyl ring replacements with respect to achieving an optimal balance of properties (e.g., γ-secretase inhibition, aqueous solubility/permeability, in vitro metabolic stability). Overall, this work enhances the scope of the [1.1.1]-bicycle beyond that of a mere spacer unit and presents a compelling case for its broader application as a phenyl group replacement in scenarios where the aromatic ring count impacts physicochemical parameters and overall drug-likeness.
