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FEBS Letters, ISSN 0014-5793, 10/2018, Volume 592, Issue 20, pp. 3380 - 3387
The coupling of the reaction of a tightly bound ubiquinone with the reduction of O 2 in cytochrome bo 3 of Escherichia coli was investigated. In the absence of... 
quinol oxidase | quinol binding site | site‐directed mutagenesis | oxygen reduction | direct electron transfer | protein film voltammetry
Journal Article
Journal of Heterocyclic Chemistry, ISSN 0022-152X, 05/2019, Volume 56, Issue 5, pp. 1634 - 1645
Isoquinolines rank as the second largest group among the plant alkaloids. Natural isoquinolines and synthetic isoquinoline derivatives exhibit numerous... 
CHEMISTRY, ORGANIC | COMPLEX | QUINOL OXIDATION SITE | DERIVATIVES
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 10/2019, Volume 361, Issue 19, pp. 4468 - 4473
A novel reactivity of dimethyldioxirane, generated in situ from Oxone and acetone, with substituted phenols and naphthols is reported. This methodology allowed... 
epoxy ortho-quinols | Oxidative dearomatization | dimethyldioxirane | Oxone | ortho-quinols | Phenols | Synthesis | Natural products | Acetone
Journal Article
Journal of Bacteriology, ISSN 0021-9193, 03/2019, Volume 201, Issue 11
Spores have strongly reduced metabolic activity and are produced during the complex developmental cycle of the actinobacterium Streptomyces coelicolor. Resting... 
Cytochrome | Reductases | Enzymes | Oxygen | Transcription | Streptomyces coelicolor | Oxidase | Quinol oxidase | Nitrates | Loci | Spores | Nitrate reduction | Mutants | Reduction | Nitrate reductase | Energy conservation | Dependence | Cytochromes | Complementation | Catalysis | Electron sources | Quinol | Cytochrome bd | Reductase
Journal Article
New Journal of Chemistry, ISSN 1144-0546, 2010, Volume 34, Issue 2, pp. 193 - 199
Hydroquinone (benzene-1,4-diol or quinol) is reported here to form co-crystals in different ratios with propan-2-ol, N,N-dimethylacetamide (DMA) and... 
COMPLEX | SPECTROSCOPY | DATABASE | MOLECULAR-CRYSTALS | CHEMISTRY | CHEMISTRY, MULTIDISCIPLINARY | QUINOL
Journal Article
Science, ISSN 0036-8075, 10/2019, Volume 366, Issue 6461, pp. 100 - 104
Hemes switch spots in a terminal oxidase Reduction of molecular oxygen to water is the driving force for respiration in aerobic organisms and is catalyzed by... 
Cytochrome | Divergence | Oxidase | Homology | Quinol oxidase | Drug development | Antiinfectives and antibacterials | Channels | Cofactors | Reduction | Mitochondria | Ubiquinone | E coli | Heme | Bacteria | Quinol | Relocation | Enzymes | Oxygen | Coliforms | Electron microscopy | Terminal oxidase | Cytochrome c | Microscopy | Ubiquinone-8 | Cytochromes | Electron transport | Cytochrome bd | Binding sites | Structure-function relationships
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 14935 - 13
The membrane-embedded quinol: fumarate reductase (QFR) in anaerobic bacteria catalyzes the reduction of fumarate to succinate by quinol in the anaerobic... 
SITE | FUMARATE REDUCTASE | WOLINELLA-SUCCINOGENES QUINOL | COMPLEX-II | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | HYPOTHESIS | SUCCINATE | TRANSMEMBRANE PROTON | BINDING | OXIDOREDUCTASES | Sulfate reduction | Anaerobic bacteria | Heme | Hydrophobicity | Electron transport | Quinol | Cofactors | Binding sites | Crystal structure | Reductase
Journal Article
Synlett, ISSN 0936-5214, 10/2016, Volume 27, Issue 16, pp. 2345 - 2351
Abstract Synthetic study on carthamin, a natural red pigment, is described. Attempts at the construction of the key quinol C -glycoside structure by oxidative... 
letter | chalcone | oxidative dearomatization | photoisomerization | carthamin | quinol C -glycoside | PART I | 2'-HYDROXYCHALCONE | HYDROGEN-ATOM TRANSFER | NATURAL-PRODUCTS | ISOMERIZATION | CHEMISTRY, ORGANIC | TINCTORIUS | FLUORIDES | quinol C-glycoside | ERYTHRINAN ALKALOIDS | DERIVATIVES | EFFICIENT
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 4766 - 10
Journal Article
by JA Jeong and SW Park and D Yoon and S Kim and HY Kang and JI Oh
Journal of Bacteriology, ISSN 0021-9193, 07/2018, Volume 200, Issue 14
Journal Article
Angewandte Chemie - International Edition, ISSN 1433-7851, 01/2016, Volume 55, Issue 2, pp. 728 - 731
  ComplexI is a crucial respiratory enzyme that conserves the energy from NADH oxidation by ubiquinone-10 (Q10) in proton transport across a membrane. Studies... 
oxidoreductases | proteoliposomes | electron transport chain | quinones | NADH | Enzymes | Cycles | Membranes | Side reactions | Fungicides | Oxidase | Chains | Quinol oxidase | Alternative oxidase | Hydrophobicity | Ubiquinone | Agrochemicals | Energy conservation | Oxidation | Catalysis | Energy transduction | Quinol | Quinone | Pesticides | Mammals | Inhibitors | Bicycles | Nicotinamide adenine dinucleotide | Ubiquinone-10 | Transport | Electron transport | Pharmaceuticals
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2017, Volume 114, Issue 48, pp. 12737 - 12742
Respiratory complex I (NADH: ubiquinone oxidoreductase), one of the largest membrane-bound enzymes in mammalian cells, powers ATP synthesis by using the energy... 
Electron transport chain | NADH:ubiquinone oxidoreductase | Mitochondria | Bioenergetics | Coenzyme Q10 | SUBMITOCHONDRIAL PARTICLES | coenzyme Q10 | electron transport chain | ALTERNATIVE OXIDASE | mitochondria | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | CHAIN | NADH | bioenergetics | ESCHERICHIA-COLI NDH-1 | BEEF-HEART | COENZYME-Q | HEART-MITOCHONDRIA | LIPID-BILAYER | Proteolipids - metabolism | Substrate Specificity | Ubiquinone - metabolism | Electron Transport Complex I - metabolism | Oxidoreductases - chemistry | Terpenes - chemistry | Thermodynamics | Terpenes - metabolism | Cattle | Electron Transport Complex I - genetics | Swine | Protein Interaction Domains and Motifs | Binding Sites | Recombinant Proteins - metabolism | Thermus thermophilus - enzymology | Gene Expression | Mitochondria, Heart - chemistry | Thermus thermophilus - chemistry | Biocatalysis | Oxidoreductases - metabolism | Protein Structure, Secondary | Oxidoreductases - genetics | Ubiquinone - analogs & derivatives | Mitochondria, Heart - enzymology | Models, Molecular | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Static Electricity | Amino Acid Motifs | Electron Transport Complex I - chemistry | Animals | Hydrophobic and Hydrophilic Interactions | Protein Binding | Kinetics | Ubiquinone - chemistry | Proteolipids - chemistry | Physiological aspects | Ubiquinones | Genetic aspects | Oxidoreductases | Research | Protons | Energy use | Oxidoreductase | Electron transfer | Quinol oxidase | Hydrophobicity | Mammalian cells | Quinones | Ubiquinol | Ubiquinone | Energy | Energy conversion | Reaction kinetics | Ubiquinone oxidoreductase | Catalysis | Quinol | Adenosine triphosphate | Translocation | NADH-ubiquinone oxidoreductase | Travel time | Quinone | Cells | Correlation analysis | Nicotinamide adenine dinucleotide | Ubiquinone-10 | Energy of dissociation | Terpenes | Binding sites | Biological Sciences
Journal Article
Journal Article
by Ning, ZJ and Chen, Z and Zhang, Q and Yan, YL and Qian, SX and Cao, Y and Tian, H
ADVANCED FUNCTIONAL MATERIALS, ISSN 1616-301X, 12/2007, Volume 17, Issue 18, pp. 3799 - 3807
Journal Article
Organic & Biomolecular Chemistry, ISSN 1477-0520, 01/2019, Volume 17, Issue 11, pp. 2972 - 2984
The zinc triflate-catalyzed highly regioselective C–P cross coupling reaction of p-quinol ethers with secondary phosphine oxides is reported. The reaction... 
Lewis acid | Cross coupling | Regioselectivity | Phosphine | Oxides | Phosphorus | Ethers | Quinol | Chemical synthesis | Crystallography | Zinc
Journal Article