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多酚的多组分合成及其作为潜在β-淀粉样蛋白聚集抑制剂的体外评价。

Multicomponent Synthesis of Polyphenols and their in vitro Evaluation as Potential β-Amyloid Aggregation Inhibitors.

机构信息

Istituto per lo Studio delle Macromolecole, Consiglio Nazionale delle Ricerche, via De Marini 6, 16149 Genova, Italy.

Department of Chemistry and Industrial Chemistry, University of Genova, via Dodecaneso 31, 16146 Genova, Italy.

出版信息

Molecules. 2019 Jul 19;24(14):2636. doi: 10.3390/molecules24142636.

Abstract

While plant polyphenols possess a variety of biological properties, exploration of chemical diversity around them is still problematic. Here, an example of application of the Ugi multicomponent reaction to the combinatorial assembly of artificial, yet "natural-like", polyphenols is presented. The synthesized compounds represent a second-generation library directed to the inhibition of β-amyloid protein aggregation. Chiral enantiopure compounds, and polyphenol-β-lactam hybrids have been prepared too. The biochemical assays have highlighted the importance of the key pharmacophores in these compounds. A lead for inhibition of aggregation of truncated protein AβpE3-42 was selected.

摘要

虽然植物多酚具有多种生物特性,但对其化学多样性的探索仍然存在问题。在这里,我们展示了 Ugi 多组分反应在人工“类天然”多酚的组合组装中的应用实例。所合成的化合物代表了第二代抑制β-淀粉样蛋白聚集的化合物库。还制备了手性对映纯化合物和多酚-β-内酰胺杂合物。生物化学测定强调了这些化合物中关键药效团的重要性。选择了一种抑制截短蛋白 AβpE3-42 聚集的先导化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d7d/6680962/86a4eda04ef3/molecules-24-02636-g001.jpg

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