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环肽构象的精细调整策略。

Strategies for Fine-Tuning the Conformations of Cyclic Peptides.

机构信息

Department of Chemistry, College of Science, Al-Nahrain University, Baghdad, Iraq.

School of Chemistry, University of New South Wales (UNSW) Sydney, New South Wales 2052, Australia.

出版信息

Chem Rev. 2020 Sep 9;120(17):9743-9789. doi: 10.1021/acs.chemrev.0c00013. Epub 2020 Aug 5.

Abstract

Cyclic peptides are promising scaffolds for drug development, attributable in part to their increased conformational order compared to linear peptides. However, when optimizing the target-binding or pharmacokinetic properties of cyclic peptides, it is frequently necessary to "fine-tune" their conformations, e.g., by imposing greater rigidity, by subtly altering certain side chain vectors, or by adjusting the global shape of the macrocycle. This review systematically examines the various types of structural modifications that can be made to cyclic peptides in order to achieve such conformational control.

摘要

环状肽是很有前途的药物开发支架,这在一定程度上归因于与线性肽相比,它们具有更高的构象有序性。然而,在优化环状肽的靶标结合或药代动力学性质时,通常需要“微调”它们的构象,例如通过增加刚性,巧妙地改变某些侧链矢量,或调整大环的整体形状。本文系统地研究了可以对环状肽进行的各种结构修饰,以实现这种构象控制。

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