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Merck

Role of sulfur chirality in the chemical processes of biology.

Chemical Society reviews (2005-06-21)
Ronald Bentley
摘要

Chiral structures profoundly influence chemical and biological processes. While chiral carbon biomolecules have received much attention, chirality is also possible in certain sulfur compounds; just as with carbon, there can be differences in the physiological behavior of chiral sulfur compounds. For instance, one drug enantiomer, Nexium (esomeprazole, a chiral sulfoxide), is used for its superior clinical properties as a proton pump inhibitor over the racemic mixture, Prilosec (Losec, omeprazole). This critical review introduces sulfur stereochemistry and nomenclature, and provides a comprehensive approach to chiral sulfur compounds and their enzymatic reactions in general and secondary metabolism. The major structural types of biological interest are sulfonium salts, sulfoxides, and sulfoximines. (103 references).

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Sigma-Aldrich
(R)-(+)-α-硫辛酸, ≥98.0% (HPLC)
Sigma-Aldrich
(S)-(−)-α -Lipoic acid, ≥97% (HPLC)