Literature DB >> 6477498

Se-Aryl selenenylthiosulphates and S-aryl sulphenylthiosulphates as thiol-blocking reagents.

N Patarasakulchai, P T Southwell-Keely.   

Abstract

Se-Aryl selenenylthiosulphates and S-aryl sulphenylthiosulphates inhibit papain at pH 5.8 much more rapidly than do the corresponding Se-aryl selenosulphates and S-aryl thiosulphates, and also more rapidly than do Se-alkyl selenosulphates. Se-p-Nitrophenyl selenenylthiosulphate and S-p-nitrophenyl sulphenylthiosulphate inactivate papain most rapidly, but the inactivation is slowly and spontaneously reversible. Inactivation by Se-o-nitrophenyl selenenylthiosulphate and S-o-nitrophenyl sulphenylthiosulphate, although less rapid than that by the para isomers, is essentially irreversible.

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Year:  1984        PMID: 6477498      PMCID: PMC1144109          DOI: 10.1042/bj2210797

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  4 in total

1.  Tissue sulfhydryl groups.

Authors:  G L ELLMAN
Journal:  Arch Biochem Biophys       Date:  1959-05       Impact factor: 4.013

2.  Specific covalent modification of thiols: applications in the study of enzymes and other biomolecules.

Authors:  K Brocklehurst
Journal:  Int J Biochem       Date:  1979

3.  Alkyl selenosulphates (seleno Bunte salts). A new class of thiol-blocking reagents.

Authors:  A R Scarf; E R Cole; P T Southwell-Keely
Journal:  Biochem J       Date:  1982-02-01       Impact factor: 3.857

4.  Susceptibility of a dwarf strain of chickens to rickets.

Authors:  R E Austic; D J Baker; R K Cole
Journal:  Poult Sci       Date:  1977-01       Impact factor: 3.352

  4 in total

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