Synthesis of the sphingolipid activator protein, saposin C, using an azido-protected O-acyl isopeptide as an aggregation-disrupting element-Reference-Cited by-同舟云学术

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Synthesis of the sphingolipid activator protein, saposin C, using an azido-protected O-acyl isopeptide as an aggregation-disrupting element

Published:2011-02 Issue:5 Volume:52 Page:635-639
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Hojo Hironobu,Katayama Hidekazu,Tano Chiharu,Nakahara Yuko,Yoneshige Azusa,Matsuda Junko,Sohma Youhei,Kiso Yoshiaki,Nakahara Yoshiaki

Funder

Japan Society for the Promotion of Science

Ministry of Education, Sports, Science and Technology of Japan

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Synthesis of Proteins by Native Chemical Ligation

2. Synthesis of Native Proteins by Chemical Ligation

3. Polypeptide Synthesis Using theS-Alkyl Thioester of a Partially Protected Peptide Segment. Synthesis of the DNA-Binding Domain ofc-Myb Protein (142–193)–NH2

4. Polypeptide synthesis by the thioester method

5. Some ‘difficult sequences’ made easy

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1. A straightforward methodology to overcome solubility challenges for N-terminal cysteinyl peptide segments used in native chemical ligation;Chemical Science;2021

2. Synthesis of Azido Acids and Their Application in the Preparation of Complex Peptides;Synthesis;2020-11-09

3. Removable Backbone Modification Method for the Chemical Synthesis of Membrane Proteins;Accounts of Chemical Research;2017-04-04

4. A strategy for the synthesis of hydrophobic proteins and glycoproteins;Organic & Biomolecular Chemistry;2016

5. Medicinal Chemistry Focusing on Aggregation of Amyloid-β;Chemical and Pharmaceutical Bulletin;2016

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