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  • naphthoquinone - 130-15-4, C10H6O2, density, melting point, boiling . . .
    naphthoquinone Molecular Formula: C 10 H 6 O 2 Molecular Weight: 158 156 g mol Cas Number: 130-15-4 EINECS Number: 204-977-6 MDL Number: MFCD00001676 InChIKey: FRASJONUBLZVQX-UHFFFAOYAK Smiles: O=C1C=CC (=O)C2=C1C=CC=C2
  • Naphthoquinone - Wikipedia
    Naphthoquinones constitute a class of organic compounds structurally related to naphthalene Two isomers are common for the parent naphthoquinones: Chemical structure of juglone, a compound produced by black walnut trees 1,2-Naphthoquinone, from the biodegradation of naphthalene
  • 1,4-Naphthoquinone | C10H6O2 | CID 8530 - PubChem
    1,4-Naphthoquinone | C10H6O2 | CID 8530 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety hazards toxicity information, supplier lists, and more
  • Naphthoquinone - an overview | ScienceDirect Topics
    Naphthoquinones are aromatic compounds derived from naphthalene, known for their conjugated cyclic dione structure and diverse bioactive properties, including anticancer, antifungal, and antiparasitic activities You might find these chapters and articles relevant to this topic 1988, Phytochemicals in Plant Cell Cultures Mamoru Tabata
  • 1,4-Naphthoquinones: Some Biological Properties and Application
    Cardioprotective, anti-ischemic, hepatoprotective, neuroprotective and some other new properties were found for these compounds; their role in protecting against neurodegenerative diseases has been established
  • Biosynthesis and molecular actions of specialized 1,4-naphthoquinone . . .
    While traditional medicine has long used 1,4-naphthoquinone-producing plants, pharmacologists are now exploring their potential to treat problems ranging from inflammation to cancer
  • Molecular mechanism and health effects of 1,2-Naphtoquinone
    It presents evidence of 1,2-NQ-mediated genotoxicity, neurogenic inflammation, and cytotoxicity due to several mechanistic properties, including the production of reactive oxygen species (ROS), that promote cell damage, carcinogenesis, and cell death
  • 1,4-Naphthoquinone 97 130-15-4 - MilliporeSigma
    1,4-Naphthoquinone was used as a potential inhibitor of monoamine oxidase and DNA topoisomerase activities [1] It was also used to inhibit the acetyltransferase activity [2]
  • 1,4-Naphthoquinone - Wikipedia
    1,4-Naphthoquinone or para-naphthoquinone is a quinone derived from naphthalene It forms volatile yellow triclinic crystals and has a sharp odor similar to benzoquinone
  • 1,4-Naphthoquinone: Biological Activity and Biomedical Applications
    1,4-Naphthoquinones are common metabolites of plants, animals, fungi and bacteria The range of biological effects of natural and synthetic 1,4-naphthoquinones is diverse and includes antimicrobial, antifungal, antiviral, antiprotozoal, wound healing, cytotoxic, antitumor and some other properties





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