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A Potent and Orally Efficacious, Hydroxyethylamine-Based Inhibitor of 尾-Secretase
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文摘
尾-Secretase inhibitors are potentially disease-modifying treatments for Alzheimer's disease. Previous efforts in our laboratory have resulted in hydroxyethylamine-derived inhibitors such as 1 with low nanomolar potency against 尾-site amyloid precursor protein cleaving enzyme (BACE). When dosed intravenously, compound 1 was also shown to significantly reduce A尾40 levels in plasma, brain, and cerebral spinal fluid. Herein, we report further optimizations that led to the discovery of inhibitor 16 as a novel, potent, and orally efficacious BACE inhibitor.

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cs.org/action/doSearch?action=search&searchText=%CE%B2%5C-site+amyloid+precursor+protein+cleaving+enzyme+%5C%28BACE%5C%29&qsSearchArea=searchText">尾-site amyloid precursor protein cleaving enzyme (BACE); cs.org/action/doSearch?action=search&searchText=Alzheimer%27s+disease+%5C%28AD%5C%29&qsSearchArea=searchText">Alzheimer's disease (AD); cs.org/action/doSearch?action=search&searchText=hydroxyethylamine+%5C%28HEA%5C%29+isostere&qsSearchArea=searchText">hydroxyethylamine (HEA) isostere

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