Medicine Design, Medicinal Chemistry , Pfizer Inc. , Cambridge , Massachusetts 02139 , United States.
Clinical & Translational Imaging, Early Clinical Development , Pfizer Inc. , Cambridge , Massachusetts 02139 , United States.
J Med Chem. 2018 Apr 26;61(8):3296-3308. doi: 10.1021/acs.jmedchem.7b01769. Epub 2018 Feb 2.
Alzheimer's disease (AD) is characterized by accumulation of β-amyloid (Aβ) plaques and neurofibrillary tau tangles in the brain. β-Site amyloid precursor protein cleaving enzyme 1 (BACE1) plays a key role in the generation of Aβ fragments via extracellular cleavage of the amyloid precursor protein (APP). We became interested in developing a BACE1 PET ligand to facilitate clinical assessment of BACE1 inhibitors and explore its potential in the profiling and selection of patients for AD trials. Using a set of PET ligand design parameters, compound 3 (PF-06684511) was rapidly identified as a lead with favorable in vitro attributes and structural handles for PET radiolabeling. Further evaluation in an LC-MS/MS "cold tracer" study in rodents revealed high specific binding to BACE1 in brain. Upon radiolabeling, [F]3 demonstrated favorable brain uptake and high in vivo specificity in nonhuman primate (NHP), suggesting its potential for imaging BACE1 in humans.
阿尔茨海默病(AD)的特征是大脑中β-淀粉样蛋白(Aβ)斑块和神经原纤维缠结的积累。β-位点淀粉样前体蛋白裂解酶 1(BACE1)通过淀粉样前体蛋白(APP)的细胞外裂解在 Aβ片段的产生中起关键作用。我们有兴趣开发一种 BACE1 PET 配体,以促进 BACE1 抑制剂的临床评估,并探索其在 AD 试验中对患者进行分析和选择的潜力。使用一组 PET 配体设计参数,化合物 3(PF-06684511)被迅速确定为具有有利的体外特性和 PET 放射性标记结构特征的先导化合物。在啮齿动物的 LC-MS/MS“冷示踪剂”研究中的进一步评估显示,[F]3 在大脑中与 BACE1 具有高特异性结合。放射性标记后,[F]3 显示出在非人灵长类动物(NHP)中良好的脑摄取和高体内特异性,表明其在人类中成像 BACE1 的潜力。