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関連する概念動画

Oxidation of Phenols to Quinones01:17

Oxidation of Phenols to Quinones

4.4K
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...
4.4K
Electron Transport Chain: Complex III and IV01:43

Electron Transport Chain: Complex III and IV

8.9K
During the electron transport chain, electrons from NADH and FADH2 are first transferred to complexes I and II, respectively. These two complexes then transfer the electrons to ubiquinol, which carries them further to complex III. Complex III passes the electrons across the intermembrane space to Cyt c, which carries them further to complex IV. Complex IV donates electrons to oxygen and reduces it to water. As electrons pass through complexes I, III, and IV, the energy released aids the pumping...
8.9K
The Electron Transport Chain01:30

The Electron Transport Chain

19.4K
The electron transport chain or oxidative phosphorylation is an exothermic process in which free energy released during electron transfer reactions is coupled to ATP synthesis. This process is a significant source of energy in aerobic cells, and therefore inhibitors of the electron transport chain can be detrimental to the cell's metabolic processes.
Inhibitors of the electron transport chain
Rotenone, a widely used pesticide, prevents electron transfer from Fe-S cluster to ubiquinone or Q...
19.4K
Electron Transport Chain: Complex I and II01:46

Electron Transport Chain: Complex I and II

18.3K
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...
18.3K
Electron Transport Chains01:28

Electron Transport Chains

111.1K
The final stage of cellular respiration is oxidative phosphorylation that consists of two steps: the electron transport chain and chemiosmosis. The electron transport chain is a set of proteins found in the inner mitochondrial membrane in eukaryotic cells. Its primary function is to establish a proton gradient that can be used during chemiosmosis to produce ATP and generate electron carriers, such as NAD+ and FAD, that are used in glycolysis and the citric acid cycle.
The ETC is comprised of...
111.1K
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

3.1K
Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
3.1K

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関連する実験動画

Updated: Jan 1, 2026

Facile Preparation of 4-Substituted Quinazoline Derivatives
11:51

Facile Preparation of 4-Substituted Quinazoline Derivatives

Published on: February 15, 2016

12.3K

化学酵素によるキノンメチド形成

Tyler J Doyon, Jonathan C Perkins, Summer A Baker Dockrey

    Journal of the American Chemical Society
    |December 17, 2019
    PubMed
    まとめ

    特定の鉄酵素を用いた生物触媒は,穏やかな条件下で反応性のあるオキノンメチド中間産物を生成する. これは,複雑な分子合成のための化学酵素カスケードで選択的なC-H結合機能化を可能にします.

    科学分野:

    • 有機化学
    • 生物触媒
    • 合成化学

    背景:

    • 自然界は分子複雑性のために 反応性の中間物質を活用しています
    • 温和な条件下での反応性種の選択的生成は,合成の課題であり続けています.

    研究 の 目的:

    • 高化学選択性のオキノンメチド中間産物を生成するためのバイオカタリシスを実証する.
    • C−H結合の機能化のための温和な水性方法を開発する.

    主な方法:

    • α-ケトグルタレットに依存する非ヘム鉄酵素 (CitBとClaD) を利用した.
    • ベンジルC-H結合のバイオカタリシスヒドロキシル化が,オクレソル基板に用いられている.
    • オキノンメチドが,単一ポット化学酵素カスケードで,核愛性/二代性によって取り込まれる.

    主要な成果:

    • 温和で水分な条件下でのベンジルC−H結合の選択的変化を達成した.
    • C-Hの債券をC-C,C-N,C-O,C-Sの債券に変換することを実証した.
    • 自然産物 (-) - キシロケタルDの選択的ペプチド改変と合成が示された.

    結論:

    さらに関連する動画

    Inner Mitochondrial Membrane Sensitivity to Na+ Reveals Partially Segmented Functional CoQ Pools
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    Inner Mitochondrial Membrane Sensitivity to Na+ Reveals Partially Segmented Functional CoQ Pools

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    Formation of Covalent DNA Adducts by Enzymatically Activated Carcinogens and Drugs In Vitro and Their Determination by 32P-postlabeling
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    関連する実験動画

    Last Updated: Jan 1, 2026

    Facile Preparation of 4-Substituted Quinazoline Derivatives
    11:51

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    Published on: February 15, 2016

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    Inner Mitochondrial Membrane Sensitivity to Na+ Reveals Partially Segmented Functional CoQ Pools
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    Inner Mitochondrial Membrane Sensitivity to Na+ Reveals Partially Segmented Functional CoQ Pools

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    Formation of Covalent DNA Adducts by Enzymatically Activated Carcinogens and Drugs In Vitro and Their Determination by 32P-postlabeling
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    Formation of Covalent DNA Adducts by Enzymatically Activated Carcinogens and Drugs In Vitro and Their Determination by 32P-postlabeling

    Published on: March 20, 2018

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  • 生物触媒は 精密な化学選択性を持つ 反応性中間物質を生成するための 強力なプラットフォームを提供します
  • この化学酵素的アプローチは,C−H結合の効率的で軽い機能化を可能にします.
  • この方法は,天然製品やペプチドを含む複雑な分子合成に適用できます.