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Se-Aryl selenenylthiosulphates and S-aryl sulphenylthiosulphates as thiol-blocking reagents.作为硫醇阻断剂的硒芳基硫代亚硫酸盐和硫芳基亚磺酰基硫代硫酸盐。
Biochem J. 1984 Aug 1;221(3):797-801. doi: 10.1042/bj2210797.
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本文引用的文献

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Tissue sulfhydryl groups.组织巯基
Arch Biochem Biophys. 1959 May;82(1):70-7. doi: 10.1016/0003-9861(59)90090-6.
2
Alkyl selenosulphates (seleno Bunte salts). A new class of thiol-blocking reagents.烷基硒代硫酸盐(硒代邦特盐)。一类新型的硫醇阻断试剂。
Biochem J. 1982 Feb 1;201(2):305-9. doi: 10.1042/bj2010305.
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Susceptibility of a dwarf strain of chickens to rickets.
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Specific covalent modification of thiols: applications in the study of enzymes and other biomolecules.硫醇的特异性共价修饰:在酶和其他生物分子研究中的应用
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作为硫醇阻断剂的硒芳基硫代亚硫酸盐和硫芳基亚磺酰基硫代硫酸盐。

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

作者信息

Patarasakulchai N, Southwell-Keely P T

出版信息

Biochem J. 1984 Aug 1;221(3):797-801. doi: 10.1042/bj2210797.

DOI:10.1042/bj2210797
PMID:6477498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1144109/
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.

摘要

硒芳基硒代硫代硫酸盐和硫芳基硫代亚磺酸盐在pH 5.8时抑制木瓜蛋白酶的速度比相应的硒芳基亚硒酸盐和硫芳基硫代硫酸盐快得多,也比硒烷基亚硒酸盐快。对硝基苯硒代硫代硫酸盐和对硝基苯硫代亚磺酸盐使木瓜蛋白酶失活最快,但失活是缓慢且自发可逆的。邻硝基苯硒代硫代硫酸盐和邻硝基苯硫代亚磺酸盐引起的失活虽然比对位异构体慢,但基本上是不可逆的。