Literature DB >> 15965542

Role of sulfur chirality in the chemical processes of biology.

Ronald Bentley1.   

Abstract

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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Year:  2005        PMID: 15965542     DOI: 10.1039/b418284g

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  29 in total

Review 1.  The biological significance of methionine sulfoxide stereochemistry.

Authors:  Byung Cheon Lee; Vadim N Gladyshev
Journal:  Free Radic Biol Med       Date:  2010-11-11       Impact factor: 7.376

2.  Functional AdoMet Isosteres Resistant to Classical AdoMet Degradation Pathways.

Authors:  Tyler D Huber; Fengbin Wang; Shanteri Singh; Brooke R Johnson; Jianjun Zhang; Manjula Sunkara; Steven G Van Lanen; Andrew J Morris; George N Phillips; Jon S Thorson
Journal:  ACS Chem Biol       Date:  2016-07-14       Impact factor: 5.100

Review 3.  Catalytic, Enantioselective Sulfenofunctionalization of Alkenes: Development and Recent Advances.

Authors:  Anastassia Matviitsuk; Jesse L Panger; Scott E Denmark
Journal:  Angew Chem Int Ed Engl       Date:  2020-08-18       Impact factor: 15.336

4.  Yeast, plants, worms, and flies use a methyltransferase to metabolize age-damaged (R,S)-AdoMet, but what do mammals do?

Authors:  Chris R Vinci; Steven G Clarke
Journal:  Rejuvenation Res       Date:  2010 Apr-Jun       Impact factor: 4.663

5.  Selective reduction of methylsulfinyl-containing compounds by mammalian MsrA suggests a strategy for improved drug efficacy.

Authors:  Byung Cheon Lee; Dmitri E Fomenko; Vadim N Gladyshev
Journal:  ACS Chem Biol       Date:  2011-08-22       Impact factor: 5.100

6.  A Baeyer-Villiger monooxygenase from Cupriavidus basilensis catalyzes asymmetric synthesis of (R)-lansoprazole and other pharmaco-sulfoxides.

Authors:  Feng Liu; Chao Shou; Qiang Geng; Chen Zhao; Jianhe Xu; Huilei Yu
Journal:  Appl Microbiol Biotechnol       Date:  2021-03-29       Impact factor: 4.813

7.  Methionine Adenosyltransferase Engineering to Enable Bioorthogonal Platforms for AdoMet-Utilizing Enzymes.

Authors:  Tyler D Huber; Jonathan A Clinger; Yang Liu; Weijun Xu; Mitchell D Miller; George N Phillips; Jon S Thorson
Journal:  ACS Chem Biol       Date:  2020-03-03       Impact factor: 5.100

Review 8.  S-adenosylmethionine in liver health, injury, and cancer.

Authors:  Shelly C Lu; José M Mato
Journal:  Physiol Rev       Date:  2012-10       Impact factor: 37.312

9.  Synthesis and antiproliferative properties of a new ceramide analog of varacin.

Authors:  Adaickapillai Mahendran; Ashwini A Ghogare; Robert Bittman; Gilbert Arthur; Alexander Greer
Journal:  Chem Phys Lipids       Date:  2015-08-05       Impact factor: 3.329

10.  Rapid methods for high-throughput detection of sulfoxides.

Authors:  Janna Shainsky; Netta-Lee Derry; Yael Leichtmann-Bardoogo; Thomas K Wood; Ayelet Fishman
Journal:  Appl Environ Microbiol       Date:  2009-05-22       Impact factor: 4.792

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