Use of a Temporary “Solubilizing” Peptide Tag for the Fmoc Solid-Phase Synthesis of Human Insulin Glargine via Use of Regioselective Disulfide Bond Formation-Reference-Cited by-同舟云学术

Use of a Temporary “Solubilizing” Peptide Tag for the Fmoc Solid-Phase Synthesis of Human Insulin Glargine via Use of Regioselective Disulfide Bond Formation

Published:2009-06-24 Issue:7 Volume:20 Page:1390-1396
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Hossain Mohammed Akhter¹,Belgi Alessia¹,Lin Feng¹,Zhang Suode¹,Shabanpoor Fazel¹,Chan Linda¹,Belyea Chris¹,Truong Hue-Trung¹,Blair Amy R.¹,Andrikopoulos Sof¹,Tregear Geoffrey W.¹,Wade John D.¹

Affiliation:

1. Howard Florey Institute, Department of Biochemistry and Molecular Biology, School of Chemistry, Department of Medicine (AH/NH), The University of Melbourne, Victoria 3010, Australia, and Metabolic Pharmaceuticals Ltd, 2/320 Lorimer Street, Port Melbourne, Victoria 3207, Australia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology

Link

https://pubs.acs.org/doi/pdf/10.1021/bc900181a

Reference41 articles.

1. The Solubility of Peptide Intermediates in Organic Solvents. Solubilizing Potential of Hexafluoro-2-propanol

2. N,O-bisFmoc derivatives ofN-(2-hydroxy-4-methoxybenzyl)-amino acids: Useful intermediates in peptide synthesis

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