Acylguanidine inhibitors of β-secretase: Optimization of the pyrrole ring substituents extending into the substrate binding pocket

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• 作者：Lee D. Jennings ; Derek C. Cole ; Joseph R. Stock ; Mohani N. Sukhdeo ; John W. Ellingboe ; Rebecca Cowling ; Guixian Jin ; Eric S. Manas ; Kristi Y. Fan ; Michael S. Malamas ; Boyd L. Harrison ; Steve Jacobsen
• 关键词：BACE-1 ; Amyloid peptide ; Aβ ; peptide ; Aspartyl protease inhibitor ; BACE-1 inhibitor ; Alzheimer’ ; s disease
• 刊名：Bioorganic and Medicinal Chemistry Letters
• 出版年：2008
• 出版时间：15 January 2008
• 年：2008
• 卷：18
• 期：2
• 页码：767-771
• 全文大小：229 K

文摘

The proteolytic enzyme β-secretase (BACE-1) produces amyloid β (Aβ) peptide, the primary constituent of neurofibrillary plaques, implicated in Alzheimer’s disease, by cleavage of the amyloid precursor protein. A small molecule inhibitor of BACE-1, (diaminomethylene)-2,5-diphenyl-1H-pyrrole-1-acetamide (1, BACE-1 IC₅₀ = 3.7 μM), was recently described, representing a new small molecule lead. Initial SAR investigation demonstrated the potential of accessing the nearby S₃ and substrate binding pockets of the BACE-1 enzyme by building substituents off one of the phenyl substituents and guanidinyl functional group. We report here the optimization of guanidinyl functional group substituents on 1, leading to potent submicromolar BACE-1 inhibitors.