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Related Concept Videos

Radical Autoxidation01:20

Radical Autoxidation

2.1K
The oxidation of an organic compound in the presence of air or oxygen is called autoxidation. For example, cumene reacts with oxygen to form hydroperoxide. Autoxidation involves initiation, propagation, and termination steps. Many organic compounds are susceptible to autoxidation—especially ethers in the presence of oxygen, which form hydroperoxides. Even though this reaction is slow, old ether bottles contain small amounts of peroxide, which leads to laboratory explosions during ether...
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Preparation and Reactions of Thiols02:33

Preparation and Reactions of Thiols

5.9K
Thiols are prepared using the hydrosulfide anion as a nucleophile in a nucleophilic substitution reaction with alkyl halides. For instance, bromobutane reacts with sodium hydrosulfide to give butanethiol.
5.9K
Electron Transport Chain: Complex I and II01:46

Electron Transport Chain: Complex I and II

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The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
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Oxidation of Phenols to Quinones01:17

Oxidation of Phenols to Quinones

2.9K
In the presence of oxidizing agents, phenols are oxidized to quinones. Quinones can be easily reduced back to phenols using mild reducing agents. The electron-donating hydroxyl group enhances the reactivity of the aromatic ring, enabling oxidation of the ring even in the absence of an α hydrogen.
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox...
2.9K
Preparation and Reactions of Sulfides02:26

Preparation and Reactions of Sulfides

4.7K
Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
4.7K
Antidotes01:17

Antidotes

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Antidotes are medicinal substances used to counteract the harmful effects of toxins or drugs in the body. They function in various ways, each uniquely designed to combat specific toxic compounds.
Specific antidotes operate by inhibiting the enzymes that control biochemical pathways, reducing the production of harmful metabolites.
An example of an antidote is atropine, which counteracts the detrimental effects of cholinesterase inhibitors. It achieves this by deactivating muscarinic receptors,...
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Use of Electron Paramagnetic Resonance in Biological Samples at Ambient Temperature and 77 K
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Organoselenium compounds beyond antioxidants.

Ritu Mamgain1, Garima Mishra2, Saumya Kriti1

  • 1Chemistry Division, School of Advanced Sciences (SAS), Vellore Institute of Technology - Chennai, Chennai, India.

Future Medicinal Chemistry
|December 23, 2024
PubMed
Summary

Organoselenium compounds are synthesized for diverse medicinal applications beyond their antioxidant roles. This review highlights their anticancer, antimicrobial, and anti-inflammatory uses over the last decade.

Keywords:
AntidiabeticOrganoselenium compoundsanti-Alzheimer’santi-cancerantimicrobialantithyroidsantiviral

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Area of Science:

  • Medicinal Chemistry
  • Organic Chemistry
  • Pharmacology

Background:

  • Organoselenium chemistry is crucial for developing biologically active compounds.
  • Early research focused on antioxidant properties of organoselenium compounds.
  • Recent advancements emphasize diverse therapeutic applications.

Purpose of the Study:

  • To review the synthesis of organoselenium compounds.
  • To explore their medicinal applications in various therapies.
  • To provide a resource for medicinal chemists.

Main Methods:

  • Literature review of organoselenium compound synthesis.
  • Analysis of studies on therapeutic applications.
  • Focus on research from the past 10 years.

Main Results:

  • Organoselenium compounds show promise in anticancer therapies.
  • Antimicrobial, antiviral, antidiabetic, and anti-inflammatory activities are documented.
  • Synthesis strategies have evolved to target specific biological properties.

Conclusions:

  • Organoselenium compounds offer a broad spectrum of therapeutic potential.
  • Continued research is vital for drug development in this field.
  • This review serves as a comprehensive guide to recent advancements.