Chapter 9. Supramolecular Interactions of Cucurbit[n]uril Homologues and Derivatives with Biomolecules and Drugs

Qian Cheng, H. Yin, Ian W. Wyman, Ruibing Wang
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引用次数: 0

Abstract

The cucurbit[n]uril (CB[n]) family is an emerging class of host molecules in the field of supramolecular chemistry with a relatively short history (except for CB[6]). The internal cavities of CB[n]s are nonpolar and hydrophobic, guarded by two carbonyl-laced portals, thus they can encapsulate not only neutral molecules via hydrophobic effects but also complex cationic species via ion–dipole interactions. Due to these unique properties, many promising discoveries of supramolecular interactions between CB[n]s and biomolecules and small organic drug molecules have emerged with potential implications in the field of pharmaceutical sciences, which have become one of the most significant areas of potential applications for CB[n]s. In this chapter, we summarize the noncovalent interactions of peptides, proteins and drug molecules with CB[n] homologues and derivatives and discuss the ability of CB[n]s to modulate the functions and bioactivities of these species through host–guest chemistry, as well as the potential of CB[n]s for protein enrichments, together with other relevant topics.
第9章。瓜类同源物及其衍生物与生物分子和药物的超分子相互作用
葫芦[n]uril (CB[n])家族是超分子化学领域中历史相对较短的一类寄主分子(CB[6]除外)。CB[n]s的内部腔是非极性和疏水的,由两个羰基连接的入口保护,因此它们不仅可以通过疏水效应封装中性分子,还可以通过离子偶极子相互作用封装复杂的阳离子物质。由于这些独特的性质,许多关于CB与生物分子和小有机药物分子之间的超分子相互作用的有希望的发现已经出现,在制药科学领域具有潜在的意义,这已经成为CB潜在应用的最重要的领域之一。在本章中,我们总结了多肽、蛋白质和药物分子与CB[n]同源物和衍生物的非共价相互作用,并讨论了CB[n]s通过主客体化学调节这些物种的功能和生物活性的能力,以及CB[n]s富集蛋白质的潜力,以及其他相关主题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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