Issue 1, 1976

1-Cyano-4-dimethylamino-pyridinium salts: new water-soluble reagents for the cyanylation of protein sulphydryl groups

Abstract

1-Cyano-4-dimethylaminopyridinium perchloroate or fluoroborate rapidly react with thiols in neutral or acidic medium: in 11 min at pH 3·6, 98% of the catalytic activity of papain is inhibited; cysteine residues nos. 7 and 19 of the reduced B-chain of bovine insulin are quantitatively cyanylated at pH 3·5, then the N-peptide bonds are selectively cleaved at pH 9·5.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1976, 21-22

1-Cyano-4-dimethylamino-pyridinium salts: new water-soluble reagents for the cyanylation of protein sulphydryl groups

M. Wakselman, E. Guibé-Jampel, A. Raoult and W. D. Busse, J. Chem. Soc., Chem. Commun., 1976, 21 DOI: 10.1039/C39760000021

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