Organoselenium Compounds in Biology and Medicine

Synthesis, Biological and Therapeutic Treatments

Vimal Kumar Jain, K Indira Priyadarsini, Vimal Kumar Jain, K Indira Priyadarsini

• Éditeur: Royal Society of Chemistry
• Année: 2017
• ISBN:
  9781788012232
• Édition: 1
• Sujet: Physical Sciences
• Sous-sujet: Organic Chemistry

Organoselenium shows incredible promise in medicine, particularly cancer therapy. This book discusses organoselenium chemistry and biology in the context of its therapeutic potential, taking the reader through synthetic techniques, bioactivity and therapeutic applications.
Divided into three sections, the first section describes synthetic advances in bioactive selenium compounds, revealing how organoselenium compound toxicity, redox properties and specificity can be further tuned. The second section explains the biophysics and biochemistry of organoselenium compounds, as well as selenoproteins. The final section closes with several chapters devoted to therapeutic and medicinal applications of organoselenium compounds, covering radioprotectors, anticancer agents and antioxidant behaviour.
With contributions from leading global experts, this book covers recent advances in the field and is an ideal reference for those researching organoselenium compounds.

Chapter 1

An Overview of Organoselenium Chemistry: From Fundamentals to Synthesis

VIMAL K. JAIN,^a

^a Chemistry Division, Bhabha Atomic Research Centre, Mumbai-400 085, India [email protected]

1.1 Introduction

Selenium is a member of the group 16 elements (O, S, Se, Te and radioactive Po), collectively known as chalcogens. It was discovered in 1817 by J.J. Berzelius in the reddish deposits that formed in the lead chambers at his sulfuric acid plant at Gripsholm in Sweden. He named the element selenium in the honour of Greek goddess ‘Selene’ meaning moon.¹

The chemistry of selenium compounds was neglected for more than a century; the entire literature² comprised only ∼200 papers until 1920 and it remained an arcane field of investigation until 1970. This slow development can be attributed to the malodorous reputation of its compounds, toxicity, the instability of certain derivatives as well as the general belief that the chemistry of selenium, due to its proximity to sulfur, would be more or less similar to that of sulfur compounds. However, such beliefs and perceptions for organoselenium compounds were defied by an exponential growth of organoselenium chemistry during past three decades or so. The following three major, interdependent factors have contributed to this rapid development of the field.

• (i) Role in organic chemistry: since its discovery in the early 1930s as an oxidizing agent for organic compounds,³ selenium dioxide (SeO₂) was used predominantly in organic synthesis until the early 1970s. However, around this time several useful reactions and processes were discovered^4–6 and the interest in organoselenium compounds was further catalysed with the publication of a monograph by Klayman and Günther.⁷ Since then, the number of reactions as well as the variety of selenium compounds have grown dramatically.⁸ Selenium can be introduced to a myriad organic substrates as an electrophile, nucleophile or even as a radical in a chemo-, regio- and stereo-selective manner.
• (ii) Organometallic chemistry and materials science: although metal complexes of seleno ligands (e.g. [PtCl₂(R₂Se)₂]; R=Me, Et, Prⁿ, Ph) were first synthesized more than a century ago,⁹ reports on organoselenium complexes appeared only sporadically until the early 1990s,¹⁰ possibly due to poorly developed synthetic processes for the desired organoselenium compounds. Selenium ligands quite often show unusual reactivity that differs from their sulfur counterparts.¹¹ Platinum group metal complexes with seleno ligands were developed as catalysts for various reactions since the 1990s,^12–14 and in some cases exhibit even better catalytic activity than the corresponding thio derivatives.¹² Further impetus to selenium chemistry comes from recent interest in semiconductor metal selenide nano-materials.^15–17 Metal selenolates have emerged as versatile single-source molecular precursors for the synthesis of nano-particles and deposition of thin films of metal selenides.
• (iii) Selenium in biology:¹⁸ selenium was long considered a poison until 1957 when Schwarz and Foltz identified it as an essential micronutrient.¹⁹ Fifteen years later selenocysteine, the 21st amino acid, was discovered at the active site of glutathione peroxidase (GPx), establishing the role of selenium in mammals.²⁰ Since then, approximately 40 seleno enzymes, exhibiting a range of functions have been identified.²¹ GPx has been extensively investigated due to its diversity of biological roles. To mimic the functions of GPx and related enzymes, several organoselenium compounds have been designed and developed. Ebselen is a promising candidate as an oxidant.²² The mechanistic aspects of the antioxidant activity of GPx have been worked out and the formation of several selenium species has been proposed during the catalytic cycle.²³

In the light of the above, an overview of organoselenium chemistry is presented in this chapter.

1.2 General Considerations

Selenium is a trace element occurring at an average level of 9×10⁻⁵% (0.09 ppm) in the earth's crust. There is substantial geographical variations in agricultural soils, giving selenium-deficient, -adequate and -excess (toxic) regions.²⁴ In general, selenium-deficient and -adequate regions are much more widespread than the selenium-excess regions. Selenium exists in various chemical forms in soil, which influences the availability of the element to plants. Selenium in food grains, legumes and vegetables occurs primarily in organic form (such as MetSe, cysSeMe, cysSeSecys, etc.) and is often referred as dietary selenium.²⁵ Keshan disease, Kashin–Beck disease and several dangerous viral infections (H1N1 influenza, SARS, HIV/AIDS, Ebola, etc.) are associated with selenium deficiency and outbreaks of them have originated either in bio-geo-chemically selenium-poor ...