Biochalcogen chemistry : the biological chemistry of sulfur, by Craig A. Bayse, Julia L. Brumaghim

By Craig A. Bayse, Julia L. Brumaghim

Biochalcogen Chemistry: The organic Chemistry of Sulfur, Selenium, and Tellurium highlights the organic makes use of of heavy chalcogens as a key region of concentration in bioinorganic chemistry and a unifying subject for study in a large choice of disciplines. contemporary achievements in those multidisciplinary efforts are offered that debate the sophisticated, but vital roles of biochalcogens in residing platforms as sulfur- and selenium-containing metabolic intermediates and items (Chapters 1 and 10) and of their oxidation whilst coordinated to metals (Chapters three and 4). Chemical and instrumental instruments for detecting sulfur and selenium species and their functionalities also are mentioned (Chapters 2 and 6), as are new instructions in biochalcogen purposes to redox scavenging, either by way of synthesis (Chapters 7 and eight) and mechanistic modeling (Chapter 9). Tellurium, without traditional organic functionality, is represented including sulfur and selenium as a phasing agent in nucleic acid crystallography and for different organic stories (Chapter 5).

This ebook will function an invaluable selection of reports and study leads to this assorted box, encompassing learn in bioinorganic chemistry, natural synthesis, computational ways, and biochemistry, as an idea for researchers wishing to go into the range of fields that surround those multidisciplinary study efforts, and as an invaluable source for undergraduate or graduate classes targeting major crew and transition point biochemistry. a large viewers will locate this e-book a invaluable source for this swiftly increasing box

Show description

Read or Download Biochalcogen chemistry : the biological chemistry of sulfur, selenium, and tellurium PDF

Similar chemistry books

Recent Advances in Chemistry and Technology of Fats and Oils

Considering that we produced fat and Oils: Chemistry and expertise in 1980, the craze we expected to up-date the classical texts of oils and fat has manifested itself. Bailey's recognized textbook has been thoroughly revised and a moment version of Bernardini's paintings has been produced. the current textual content is an try to supply a few perception into the present state-of-the-art.

Inverse Gas Chromatography. Characterization of Polymers and Other Materials

Content material: evaluation of inverse gasoline chromatography / Henry P. Schreiber and Douglas R. Lloyd -- Experimental options for inverse gasoline chromatography / A. E. Bolvari, Thomas Carl Ward, P. A. Koning, and D. P. Sheehy -- reports of polymer constitution and interactions by way of computerized inverse fuel chromatography / James E.

Chemistry of Heterocyclic Compounds: Small Ring Heterocycles, Part 3: Oxiranes, Arene Oxides, Oxaziridines, Dioxetanes, Thietanes, Thietes, Thiazetes, and Others, Volume 42

Oxiranes (M. Bartok and okay. Lang). Arene Oxides-Oxpins (D. Boyd and D. Jerina). Oxaziridines (M. Haddadin and J. Freeman). Dioxetanes and a-Peroxylactones (W. Adam and F. Yany). 4-membered Sulfur Heterocycles (D. Dittmer and T. Sedergran). writer and topic Indexes. content material: bankruptcy I Oxiranes (pages 1–196): M.

Additional resources for Biochalcogen chemistry : the biological chemistry of sulfur, selenium, and tellurium

Example text

2011, 18, 282–286. 73. ; Palm, G. ; Pellecchia, C. Inorg. Chem. 2012, 51, 11220–11222. 74. ; Han, K. Chem. Commun. 2013, 49, 1014–1016. ; ACS Symposium Series; American Chemical Society: Washington, DC, 2013. ch003 Chapter 3 Thione- and Selone-Containing Compounds, Their Late First Row Transition Metal Coordination Chemistry, and Their Biological Potential Bradley S. Stadelman and Julia L. edu. Thione- and selone-containing compounds and their transition metal complexes have been investigated for purposes ranging from antioxidant and anti-tumor activity to materials for optical electronics and light emitting diodes.

A. Am. J. Physiol-Reg I 2006, 291, R491–R511. 5. Olson, K. R. Antioxid. Redox Signaling 2012, 17, 32–44. 6. Wang, R. Physiol. Rev. 2012, 92, 791–896. 7. Pluth, M. ; Lippard, S. J. Annu. Rev. Biochem. 2011, 80, 333−355. 8. ; Kimura, H. Antioxid. Redox Signaling 2009, 11, 205–214. 9. Toohey, J. I. Biochem. J. 1989, 264, 625–632. 10. ; Kimura, H. Biochem. Biophys. Res. Commun. 1997, 237, 527–531. 11. ; Pattillo, C. ; Bir, S. ; Kevil, C. G. Free Radical Biol. Med. 2011, 50, 1021–1031. 12. ; Kimura, H.

J. Am. Chem. Soc. 2011, 133, 10078–10080. 32. Lin, V. ; Lippert, A. ; Chang, C. J. Proc. Natl. Acad. Sci. A. 2013, 110, 7131–7135. 33. ; Han, K. Chem. Commun. 2012, 48, 2852–2854. 34. Montoya, L. ; Pluth, M. D. Chem. Commun. 2012, 48, 4767–4769. 35. ; Zhang, W. Anal. Chim. Acta 2013, 768, 136–142. 36. ; Wu, S. Chem. Commun. 2013, 49, 403–405. 37. ; Wang, W. Chem. Commun. 2012, 48, 10669–10671. 38. ; King, A. ; Predmore, B. ; Lefer, D. ; Wang, B. Angew. , Int. Ed. 2011, 50, 9672–9675. ; ACS Symposium Series; American Chemical Society: Washington, DC, 2013.

Download PDF sample

Rated 4.49 of 5 – based on 24 votes