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For: Agouridas V, El Mahdi O, Melnyk O. Chemical Protein Synthesis in Medicinal Chemistry. J Med Chem 2020;63:15140-52. [PMID: 33236900 DOI: 10.1021/acs.jmedchem.0c01082] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 4.3] [Reference Citation Analysis]
Number Citing Articles
1 Harel O, Jbara M. Chemical Synthesis of Bioactive Proteins. Angew Chem Int Ed Engl 2023;62:e202217716. [PMID: 36661212 DOI: 10.1002/anie.202217716] [Reference Citation Analysis]
2 Wu H, Tan Y, Ngai WL, Li X. Total synthesis of interleukin-2 via a tunable backbone modification strategy. Chem Sci 2023;14:1582-9. [PMID: 36794182 DOI: 10.1039/d2sc05660g] [Reference Citation Analysis]
3 Ollivier N, Sénéchal M, Desmet R, Snella B, Agouridas V, Melnyk O. A biomimetic electrostatic assistance for guiding and promoting N-terminal protein chemical modification. Nat Commun 2022;13:6667. [PMID: 36335111 DOI: 10.1038/s41467-022-34392-5] [Reference Citation Analysis]
4 Nakatsu K, Okamoto A, Hayashi G, Murakami H. Repetitive Thiazolidine Deprotection Using a Thioester‐Compatible Aldehyde Scavenger for One‐Pot Multiple Peptide Ligation**. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202206240] [Reference Citation Analysis]
5 Agouridas V, Ollivier N, Vicogne J, Diemer V, Melnyk O. Redox-Controlled Chemical Protein Synthesis: Sundry Shades of Latency. Acc Chem Res 2022;55:2685-97. [PMID: 36083810 DOI: 10.1021/acs.accounts.2c00436] [Reference Citation Analysis]
6 Snella B, Grain B, Vicogne J, Capet F, Wiltschi B, Melnyk O, Agouridas V. Fast Protein Modification in the Nanomolar Concentration Range Using an Oxalyl Amide as Latent Thioester. Angew Chem Int Ed Engl 2022;61:e202204992. [PMID: 35557487 DOI: 10.1002/anie.202204992] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Li J, Hu Q, Song Z, Chan ASC, Xiong X. Cleavable Cys labeling directed Lys site-selective stapling and single-site modification. Sci China Chem . [DOI: 10.1007/s11426-022-1252-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Diemer V, Firstova O, Agouridas V, Melnyk O. Pedal to the Metal: The Homogeneous Catalysis of the Native Chemical Ligation Reaction. Chemistry 2022;28:e202104229. [PMID: 35048443 DOI: 10.1002/chem.202104229] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
9 Wang S, Zhou Q, Li Y, Wei B, Liu X, Zhao J, Ye F, Zhou Z, Ding B, Wang P. Quinoline-Based Photolabile Protection Strategy Facilitates Efficient Protein Assembly. J Am Chem Soc 2022. [PMID: 35034454 DOI: 10.1021/jacs.1c10324] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
10 Dao Y, Wang B, Dong W, Zhang J, Zhong C, Zhang Z, Dong S. Facile Generation of Strained Peptidyl Thiolactones from Hydrazides and Its Application in Assembling MUC ‐1 VNTR Oligomers . Chin J Chem 2021;39:2509-16. [DOI: 10.1002/cjoc.202100326] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
11 Jbara M, Pomplun S, Schissel CK, Hawken SW, Boija A, Klein I, Rodriguez J, Buchwald SL, Pentelute BL. Engineering Bioactive Dimeric Transcription Factor Analogs via Palladium Rebound Reagents. J Am Chem Soc 2021;143:11788-98. [PMID: 34289685 DOI: 10.1021/jacs.1c05666] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 3.0] [Reference Citation Analysis]
12 Li Y, Liu J, Zhou Q, Zhao J, Wang P. Preparation of Peptide Selenoesters from Their Corresponding Acyl Hydrazides . Chin J Chem 2021;39:1861-6. [DOI: 10.1002/cjoc.202100086] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
13 Kerdraon F, Bogard G, Snella B, Drobecq H, Pichavant M, Agouridas V, Melnyk O. Insights into the Mechanism and Catalysis of Peptide Thioester Synthesis by Alkylselenols Provide a New Tool for Chemical Protein Synthesis. Molecules 2021;26:1386. [PMID: 33806630 DOI: 10.3390/molecules26051386] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]