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多价糖缀合物合成中的设计与创意。

Design and creativity in synthesis of multivalent neoglycoconjugates.

出版信息

Adv Carbohydr Chem Biochem. 2010;63:165-393. doi: 10.1016/S0065-2318(10)63006-5.

Abstract

From the authors' opinion, this chapter constitutes a modest extension of the seminal and inspiring contribution of Stowell and Lee on neoglycoconjugates published in this series [C. P. Stowell and Y. C. Lee, Adv. Carbohydr. Chem. Biochem., 37 (1980) 225-281]. The outstanding progresses achieved since then in the field of the "glycoside cluster effect" has witnessed considerable creativity in the design and synthetic strategies toward a vast array of novel carbohydrate structures and reflects the dynamic activity in the field even since the recent chapter by the Nicotra group in this series [F. Nicotra, L. Cipolla, F. Peri, B. La Ferla, and C. Radaelli, Adv. Carbohydr. Chem. Biochem., 61 (2007) 353-398]. Beyond the more classical neoglycoproteins and glycopolymers (not covered in this work) a wide range of unprecedented and often artistically beautiful multivalent and monodisperse nanostructures, termed glycodendrimers for the first time in 1993, has been created. This chapter briefly surveys the concept of multivalency involved in carbohydrate-protein interactions. The topic is also discussed in regard to recent steps undertaken in glycobiology toward identification of lead candidates using microarrays and modern analytical tools. A systematic description of glycocluster and glycodendrimer synthesis follows, starting from the simplest architectures and ending in the most complex ones. Presentation of multivalent glycostructures of intermediate size and comprising, calix[n]arene, porphyrin, cyclodextrin, peptide, and carbohydrate scaffolds, has also been intercalated to better appreciate the growing synthetic complexity involved. A subsection describing novel all-carbon-based glycoconjugates such as fullerenes and carbon nanotubes is inserted, followed by a promising strategy involving dendrons self-assembling around metal chelates. The chapter then ends with those glycodendrimers that have been prepared using commercially available dendrimers possessing varied functionalities, or systematically synthesized using either divergent or convergent strategies.

摘要

从作者的观点来看,本章是对 Stowell 和 Lee 在本系列中发表的关于糖基化缀合物开创性和鼓舞人心的贡献的适度扩展[C. P. Stowell 和 Y. C. Lee,Adv. Carbohydr. Chem. Biochem.,37(1980)225-281]。自那时以来,在“糖苷簇效应”领域取得的杰出进展见证了在设计和合成策略方面对大量新型碳水化合物结构的创造力,并反映了该领域自本系列中 Nicotra 小组最近一章以来的动态活性[F. Nicotra、L. Cipolla、F. Peri、B. La Ferla 和 C. Radaelli,Adv. Carbohydr. Chem. Biochem.,61(2007)353-398]。除了更经典的糖基化蛋白和糖聚合物(本工作未涵盖)之外,还创造了广泛的前所未有的、通常具有艺术美感的多价和单分散纳米结构,这些结构在 1993 年首次被称为糖基树突。本章简要概述了碳水化合物-蛋白质相互作用中涉及的多价性概念。该主题还讨论了糖生物学领域为使用微阵列和现代分析工具鉴定先导候选物而采取的最新步骤。接下来系统地描述了糖基簇和糖基树突的合成,从最简单的结构开始,一直到最复杂的结构。还穿插介绍了具有中等大小的多价糖结构,包括杯[n]芳烃、卟啉、环糊精、肽和碳水化合物支架,以更好地了解所涉及的不断增加的合成复杂性。描述了新型全碳基糖缀合物,如富勒烯和碳纳米管的小节,随后是一种涉及树突自组装在金属配合物周围的有前途的策略。然后,这一章以使用具有不同功能的商业上可用的树突或使用发散或收敛策略系统地合成的那些糖基树突结束。

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