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固相合成 N-取代甘氨酸寡聚物(α-肽)及其衍生物。

Solid-phase synthesis of N-substituted glycine oligomers (alpha-peptoids) and derivatives.

机构信息

Atlantic Cancer Research Institute, Moncton, NB, Canada.

出版信息

Molecules. 2010 Aug 4;15(8):5282-335. doi: 10.3390/molecules15085282.

Abstract

Peptoids (N-substituted polyglycines and extended peptoids with variant backbone amino-acid monomer units) are oligomeric synthetic polymers that are becoming a valuable molecular tool in the biosciences. Of particular interest are their applications to the exploration of peptoid secondary structures and drug design. Major advantages of peptoids as research and pharmaceutical tools include the ease and economy of synthesis, highly variable backbone and side-chain chemistry possibilities. At the same time, peptoids have been demonstrated as highly active in biological systems while resistant to proteolytic decay. This review with 227 references considers the solid-phase synthetic aspects of peptoid preparation and utilization up to 2010 from the instigation, by R. N. Zuckermann et al., of peptoid chemistry in 1992.

摘要

肽缩氨酸(N-取代聚甘氨酸和具有不同主链氨基酸单体单元的扩展肽缩氨酸)是一种正在成为生物科学中非常有价值的分子工具的低聚合成聚合物。特别感兴趣的是它们在探索肽缩氨酸二级结构和药物设计中的应用。肽缩氨酸作为研究和药物工具的主要优势包括合成的简便性和经济性、高度可变的主链和侧链化学可能性。与此同时,肽缩氨酸在生物系统中表现出高度的活性,同时抵抗蛋白水解降解。这篇综述共有 227 篇参考文献,考虑了肽缩氨酸的固相合成方面,从 1992 年由 R. N. Zuckermann 等人发起的肽缩氨酸化学开始,直到 2010 年。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8efb/6257730/dc4c33699120/molecules-15-05282-g001.jpg

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