Infrared Absorption Study of Human Proinsulin C-Peptide Fragments in the Solid State
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/59/8/59_8_2439/_pdf
Reference31 articles.
1. Design of the Synthetic Route for Peptides and Proteins Based on the Solubility Prediction Method. I. Synthesis and Solubility Properties of Human Proinsulin C-Peptide Fragments
2. Symbols for Amino-Acid Derivatives and Peptides
3. Design of the Synthetic Route for Peptides and Proteins Based on the Solubility Prediction Method. I. Synthesis and Solubility Properties of Human Proinsulin C-Peptide Fragments
4. Prediction and improvement of protected peptide solubility in organic solvents*
5. Critical Peptide Size for Insolubility Caused by a β-Sheet Aggregation and Solubility Improvement in Hydrophobic Peptides by Replacement of Alanine Residues with α-Aminoisobutyric Acid Residues
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2. Evaluation of the Trifluoromethanosulfonic Acid/Trifluoroacetic Acid/Thioanisole Cleavage Procedure for Application in Solid-Phase Peptide Synthesis.;Chemical and Pharmaceutical Bulletin;2001
3. The Influence ofβ-Alanine and 4-Aminobutyric Acid Residues on the Solubility of Peptides Containing Them;Bulletin of the Chemical Society of Japan;1993-07
4. The Solubility and Conformation of Protected Tri- to Heptapeptides in a Variety of Organic Solvents and the Classification of Organic Solvents Based on Their Solvating Potential for Protected Peptides;Bulletin of the Chemical Society of Japan;1993-02
5. The Classification of Twenty Common Amino Acid Residues in Protected Peptides by Theirβ-Sheet-Structure-Stabilizing Potentials, SPβ, and Its Application to Peptide Synthesis;Bulletin of the Chemical Society of Japan;1993-02
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