112806-12-9Relevant academic research and scientific papers
Synthesis, redox properties, and conformational analysis of vicinal disulfide ring mimics
Ruggles, Erik L.,Deker, P. Bruce,Hondal, Robert J.
experimental part, p. 1257 - 1267 (2009/05/07)
A vicinal disulfide ring (VDR) results from disulfide-bond formation between two adjacent cysteine residues. This eight-membered ring is a rare motif in protein structures and is functionally important to those few proteins that posses it. This article focuses on the construction of strained and unstrained VDR mimics, discernment of the preferred conformation of these mimics, and the determination of their respective disulfide redox potentials.
Novel dimercaptoamides, compositions comprising them as reducing agents, and processes for permanently reshaping keratin fibers therewith
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Page/Page column 17-18, (2010/02/15)
The present disclosure relates to specific dimercaptoamides, reducing compositions for permanently reshaping keratin fibers comprising the dimercaptoamides, for instance, human keratin fibers such as the hair; and processes for reshaping keratin fibers comprising the application of said reducing compositions. The present disclosure also relates to processes for preparing the dimercaptoamides.
