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Unusual behaviour of a hydrophobic benzimidazolemethanethiol in micellar esterolysis

✍ Scribed by N. Krati; A. Brembilla; P. Lochon


Book ID
104232772
Publisher
Elsevier Science
Year
1989
Tongue
French
Weight
208 KB
Volume
30
Category
Article
ISSN
0040-4039

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✦ Synopsis


Description

of the unusual behaviour of the first term of a new series of straight-chain heterocyclic thiols (benzimidazolemethanethiols) in a micellar system, in the hydrolysis reaction of p-nitrophenylesters.

Cysteine proteases form a large class of enzymes, and their active site is known to contain both a cysteine thiol group and an imidazole heterocycle borne by a histidine residue.

In the field of enzyme model reactions, we have reported


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