Adamantyl amino acid as γ-turn inducer for peptide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Conformationally restricted peptides through short-range cyclizations
2. Emerging approaches in the molecular design of receptor-selective peptide ligands: conformational, topographical and dynamic considerations
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Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Influence of the C‐terminal substituent on the crystal‐state conformation of Adm peptides;Peptide Science;2019-05-17
2. Isolated α-turn and incipient γ-helix;Chemical Science;2019
3. Designing Peptidomimetics;Current Topics in Medicinal Chemistry;2018-07-09
4. Design, Synthesis, and In Vitro Evaluation of Novel Histone H3 Peptide-Based LSD1 Inactivators Incorporating α,α-Disubstituted Amino Acids with γ-Turn-Inducing Structures;Molecules;2018-05-06
5. En route towards the peptideγ-helix: X-ray diffraction analyses and conformational energy calculations of Adm-rich short peptides;Journal of Peptide Science;2016-12-22
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