化学
成核
单体
纤维
合理设计
生物物理学
动力学
小分子
分子
淀粉样蛋白(真菌学)
延伸率
淀粉样纤维
蛋白质聚集
组合化学
生物化学
淀粉样β
聚合物
纳米技术
生物
材料科学
有机化学
医学
无机化学
物理
疾病
病理
量子力学
极限抗拉强度
冶金
作者
Li Gao,Wuyue Yang,Wenhao Li,Yun‐Yi Luo,Yeh‐Jun Lim,Yang Li,Ashim Paul,Daniel Segal,Liu Hong,Yanmei Li
标识
DOI:10.1002/chem.201905621
摘要
It has been reported that many molecules could inhibit the aggregation of Aβ (amyloid-β) through suppressing either primary nucleation, secondary nucleation, or elongation processes. In order to suppress multiple pathways of Aβ aggregation, we screened 23 small molecules and found two types of inhibitors with different inhibiting mechanisms based on chemical kinetics analysis. Trp-glucose conjugates (AS2) could bind with fibril ends while natural products (D3 and D4) could associate with monomers. A cocktail of these two kinds of molecules achieved co-inhibition of various fibrillar species and avoid unwanted interference.
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