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Chemical protein synthesis-assisted high-throughput screening strategies for D-peptides in drug discovery 被引量:1

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摘要 D-peptides are recognized as a new class of synthetic chemical drugs and they possess many interesting advantages such as high enzymatic stability,improved oral bioavailability,as well as high binding affinity and specificity.Recently,D-peptide drugs have been attracting increasing attention in both academic and industrial researches over recent years.One D-peptide etelcalcetide has even entered the market that targets the calcium(Ca2+)-sensing receptor(CaSR) to fight secondary hyperparathyroidism.Effective discovery and optimization of D-peptide ligands that can bind to various disease-related targets with high specificity and potency is of great importance for the development of D-peptide drugs.This review surveys the recent method development in this area especially the chemical protein synthesis-assisted high-throughput screening strategies for D-peptide ligands and their application in drug discovery.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2020年第9期2365-2374,共10页 中国化学快报(英文版)
基金 supported by the National Key R&D Program of China(No.2019YFA0706902) National Natural Science Foundation of China(Nos.U1732161 and 91753120) Science and Technological Fund of Anhui Province for Outstanding Youth(No.1808085J04)。
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