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Mostrando 41 - 60 Resultados de 20,270 Para Buscar 'Flavina~', tiempo de consulta: 2.89s Limitar resultados
  1. 41
    “…To this end, molecular oxygen is activated by flavin, heme, or metal cofactor-containing enzymes and transferred to initially obtain N-hydroxy compounds, which can be further functionalized. …”
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    Flavin-dependent N-hydroxylating enzymes: distribution and application
  2. 42
    “…Although flavin-dependent halogenases (FDHs) are attractive biocatalysts, their practical applications are limited because of their low catalytic efficiency. …”
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    Dissecting the low catalytic capability of flavin-dependent halogenases
  3. 43
    “…Identifying suitable enzymes that catalyze enantioselective halocyclization of simple olefins would therefore have significant synthetic value. Flavin-dependent halogenases (FDHs) catalyze halogenation of arene and enol(ate) substrates. …”
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    Flavin-dependent halogenases catalyze enantioselective olefin halocyclization
  4. 44
    “…The photophysical properties of anionic semireduced flavin radicals are largely unknown despite their importance in numerous biochemical reactions. …”
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    Ultrafast photooxidation of protein-bound anionic flavin radicals
  5. 45
    “…This method can be used to rank a series of flavins based on their photosensitizing activities. …”
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    Investigating the photosensitization activities of flavins irradiated by blue LEDs
  6. 46
    Publicado 1860
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    Platina and Its Accompanying Metals
  7. 47
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    Platina and the Metals Which Accompany It
  8. 48
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    Platina and Its Accompanying Metals
  9. 49
    Publicado 1874
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    Golden Farina Cologne
  10. 50
    “…Oxygenase activity of the flavin-dependent enzyme RutA is commonly associated with the formation of flavin-oxygen adducts in the enzyme active site. …”
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    QM/MM Modeling of the Flavin Functionalization in the RutA Monooxygenase
  11. 51
    “…MonCI, with its ability to perform multiple epoxidations on the same substrate in a stereospecific manner, demonstrates the extraordinary versatility of the flavin-dependent monooxygenase family of enzymes.…”
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    Triepoxide formation by a flavin-dependent monooxygenase in monensin biosynthesis
  12. 52
    “…Our current work focuses on an attempted to dock this inhibitors Flavin and Phenosafranine to curtail the action of human RNR2. …”
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    A docking model of human ribonucleotide reductase with flavin and phenosafranine
  13. 53
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    Remaining challenges in cellular flavin cofactor homeostasis and flavoprotein biogenesis
  14. 54
    “…In addition, we review current progress in the search for inhibitors of flavin dependent thymidylate synthase as potential novel therapeutics.…”
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    Flavin-Dependent Thymidylate Synthase as a New Antibiotic Target
  15. 55
    “…Here we report on a flow battery using an aqueous electrolyte based on the sodium salt of flavin mononucleotide. Flavins are highly versatile electroactive molecules, which catalyse a multitude of redox reactions in biological systems. …”
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    A biomimetic redox flow battery based on flavin mononucleotide
  16. 56
    “…Flavin-dependent halogenases are potentially valuable biocatalysts for the regioselective halogenation of aromatic compounds. …”
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    Extending the biocatalytic scope of regiocomplementary flavin-dependent halogenase enzymes
  17. 57
    “…In the current research we propose non-toxic flavin mononucleotide (FMN), which is a water-soluble form of riboflavin (vitamin B2) as a promising agent for photodynamic therapy of melanoma. …”
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    Photodynamic therapy of melanoma by blue-light photoactivation of flavin mononucleotide
  18. 58
    “…The recently described flavin‐dependent halogenase BrvH is able to catalyse both the bromination and chlorination of indole, but shows significantly higher bromination activity. …”
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    Predicting the Substrate Scope of the Flavin‐Dependent Halogenase BrvH
  19. 59
    “…Flavin-Containing Monooxygenases are conserved xenobiotic-detoxifying enzymes. …”
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    Flavin-Containing Monooxygenases Are Conserved Regulators of Stress Resistance and Metabolism
  20. 60
    “…Our findings extend the repertoire of known flavin chemistry that may provide new and useful tools for organic synthesis.…”
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    Flavin-enabled reductive and oxidative epoxide ring opening reactions
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