Formation of truncated peptide by-products via sequence-specific formyl group transfer from Trp(For) residues toNαin the course of Boc-SPPS-Reference-Cited by-同舟云学术

Formation of truncated peptide by-products via sequence-specific formyl group transfer from Trp(For) residues toNαin the course of Boc-SPPS

Published:2013-08-26 Issue:10 Volume:19 Page:607-612
ISSN:1075-2617
Container-title:Journal of Peptide Science
language:en
Short-container-title:J. Pept. Sci.

Author:

Azev Viatcheslav N.¹,Mustaeva Leila G.¹,Gorbunova Elena Yu.¹,Molchanov Maksim V.²,Rodionov Igor L.¹

Affiliation:

1. Branch of Shemyakin and Ovchinnikov Bioorganic Chemistry Institute; Russian Academy of Sciences; Science Avenue, 6; Pushchino; Moscow Region; 142290; Russia

2. Institute for Theoretical and Experimental Biophysics; Russian Academy of Sciences; Institutskaya Str., 3; Pushchino; Moscow Region; 142290; Russia

Publisher

Wiley

Subject

Organic Chemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry,Structural Biology

Reference18 articles.

1. A reversible chemical modification of the tryptophan residue;Previero;Biochim. Biophys. Acta,1967

2. Improved solid-phase synthesis of tryptophan-containing peptides. I. Use of hydrogen chloride in formic acid as a reagent for the cleavage of t-butyloxycarbonyl group;Ohno;Bull. Chem. Soc. Jpn.,1972

3. Protection of tryptophan with the formyl group in peptide synthesis;Yamashiro;J. Org. Chem.,1973

4. Improved solid-phase synthesis of tryptophan-containing peptides. II. Use of Nα-t-butyloxycarbonyl-Ni-formyltryptophan;Ohno;Bull. Chem. Soc. Jpn.,1973

5. Synthesis of a pentekontapeptide with high lipolytic activity corresponding to the carboxyl-terminal fifty amino acids of ovine β-lipotropin;Yamashiro;Proc. Natl. Acad. Sci. U. S. A.,1974

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