二硫键
固相合成
折叠(DSP实现)
肽
组合化学
化学
立体化学
环肽
生物化学
工程类
电气工程
作者
Hong‐Kui Cui,Ye Guo,Yao He,Fengliang Wang,Haonan Chang,Yujia Wang,Fangming Wu,Changlin Tian,Lei Liu
标识
DOI:10.1002/anie.201302197
摘要
The antimicrobial peptide tachyplesin I was used as a model to apply the title strategy, which was developed for the preparation of peptidic macrocycles with double disulfide surrogates. The folding and activity of the tachyplesin I analogues were found to be sensitive to the structure of the disulfide surrogates, thus underlining the necessity of a flexible synthetic route for generating disulfide bond surrogates with high structural diversity.
科研通智能强力驱动
Strongly Powered by AbleSci AI