Total Synthesis of Human Hepcidin through Regioselective Disulfide-Bond Formation by using the Safety-Catch Cysteine Protecting Group 4,4′-Dimethylsulfinylbenzhydryl-Reference-Cited by-同舟云学术

Total Synthesis of Human Hepcidin through Regioselective Disulfide-Bond Formation by using the Safety-Catch Cysteine Protecting Group 4,4′-Dimethylsulfinylbenzhydryl

Published:2014-02-07 Issue:11 Volume:53 Page:2931-2934
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Dekan Zoltan,Mobli Mehdi,Pennington Michael W.,Fung Eileen,Nemeth Elizabeta,Alewood Paul F.

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference39 articles.

1. Regulation of Iron Metabolism by Hepcidin

2. The Solution Structure of Human Hepcidin, a Peptide Hormone with Antimicrobial Activity That Is Involved in Iron Uptake and Hereditary Hemochromatosis

3. Hepcidin Revisited, Disulfide Connectivity, Dynamics, and Structure

4. NMR methods for determining disulfide-bond connectivities

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