Synthesis and catalytic properties of the pentapeptide, Thr-Ala-Cys-His-Asp

I Photaki, V Bardakos, AW Lake, G Lowe - Journal of the Chemical …, 1968 - pubs.rsc.org
The pentapeptide, Thr-Ala-Cys-His-Asp, has been synthesised by use of S-diphenylmethyl-
protected cysteine. The catalytic activity towards p-nitrophenyl acetate was comparable with …

N im-p-methoxyphenylsulphonylhistidine, a new derivative for peptide synthesis

K Kitagawa, K Kitade, Y Kiso, T Akita… - Journal of the …, 1979 - pubs.rsc.org
The p-methoxyphenylsulphonyl group attached at the Nim function of histidine can be
quantitatively cleaved by trifluoroacetic acid in the presence of dimethyl sulphide at room …

A new method for the protection of the sulfhydryl group during peptide synthesis

S Akabori, S Sakakibara, Y Shimonishi… - Bulletin of the Chemical …, 1964 - jlc.jst.go.jp
The protection of the thiol group in the cysteine residue is of great importance in the field of
peptide synthesis. Glutathione, oxytocin and vasopressin have been synthesized by many …

tert-Butyl group as thiol protection in peptide synthesis

JJ Pastuszak, A Chimiak - The Journal of Organic Chemistry, 1981 - ACS Publications
S-ieri-Butylcysteine was obtained by a new method. A number of its N-protected
derivativesand esters were synthesized. Syntheses of several peptides containing tert-butyl …

Allylic protection of thiols and cysteine. III. Use of Fmoc-Cys (Fsam)-OH for solid-phase peptide synthesis

P Gomez-Martinez, F Guibé, F Albericio - Letters in Peptide Science, 2000 - Springer
The solid-phase synthesis of peptides containing Cys hasbeen carried out using the new
thiol protecting group Fsam, which is completely stable to basic and acidic conditionsused in …

Convenient solid phase synthesis method for the preparation of cysteine C-terminally derivatized peptides

NGJ Delaet, T Tsuchida - Letters in Peptide Science, 1996 - Springer
This paper describes a novel solid phase peptide synthesis method for the systematic C-
terminal modification of cysteine-containing peptides. In this method, cysteine is linked to …

Synthese und katalytische Eigenschaften hydrolytisch aktiver Peptide/Synthesis and Catalytic Properties of Peptides with Hydrolytic Activity

D Petz, F Schneider - Zeitschrift für Naturforschung C, 1976 - degruyter.com
The synthesis by conventional methods of the peptides Z-Asp-Cys-NH2, Z-Asp-Gly-Cys-
NH2, Z-Glu-Gly-Cys-NH2, Z-His-Ala-Gly-Gly-Cys-NH2, Z-His-Ala-Asp-Gly-Cys-NH2 and Z …

A new carboxy-protecting group for peptide synthesis and its direct conversion into an activated ester suitable for peptide formation: 4-(methylthio) phenyl and 4 …

BJ Johnson, PM Jacobs - Chemical Communications (London), 1968 - pubs.rsc.org
WE have found a new carboxy-protecting group, 4-(methy1thio) phenyl ester (MTP), which
can be oxidized to the sulphoxide, 4-(methylsulphiny1)-phenyl ester, and further oxidized to …

A Re-examination of two linear pentapeptides claimed to be serine protease mimics

AM Vandersteen, KD Janda - Journal of the American Chemical …, 1996 - ACS Publications
The synthesis, characterization, and kinetic study of two linear pentapeptides l-threonyl-l-
alanyl-l-seryl-l-histidyl-l-aspartic acid (TASHD) and l-seryl-γ-aminobutyryl-l-histidyl-γ …

Protection of cysteine and histidine by the diphenyl-4-pyridylmethyl group during peptide synthesis

S Coyle, GT Young - Journal of the Chemical Society, Chemical …, 1976 - pubs.rsc.org
Protection of cysteine and histidine by the diphenyl-4-pyridylmethyl group during peptide
synthesis - Journal of the Chemical Society, Chemical Communications (RSC Publishing) Jump …