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  • Menadione - Wikipedia
    Menadione is a natural [3] organic compound with the formula C 6 H 4 (CO) 2 C 2 H (CH 3) It is an analog of 1,4-naphthoquinone with a methyl group in the 2-position [4] It is sometimes called vitamin K3 Use is allowed as a nutritional supplement in animal feed because of its vitamin K activity
  • Vitamin K3 (Menadione): Benefits, Uses, and Side Effects
    Vitamin K3, also known as menadione, is a synthetic or artificially produced form of vitamin K This article explains everything you need to know about vitamin K3, including its benefits, uses,
  • Menadione | C11H8O2 | CID 4055 - PubChem
    Menadione is a member of the class of 1,4-naphthoquinones that is 1,4-naphthoquinone which is substituted at position 2 by a methyl group It is used as a nutritional supplement and for the treatment of hypoprothrombinemia
  • K3 Spark Mineral Side Effects: What You Need to Know - Greatist
    Key takeaways Vitamin K3 (menadione) is a synthetic form of vitamin K that can be harmful to humans, potentially causing liver damage, jaundice, and anemia
  • Menadione - an overview | ScienceDirect Topics
    Menadione is defined as a synthetic precursor of vitamin K that has no cofactor activity itself but can be converted in vivo to the biologically active menaquinone-4 (MK-4)
  • Menadione – Uses, Dosage, Side Effects Precautions
    Learn about Menadione, including its uses for vitamin K deficiency, recommended dosage, potential side effects, and special precautions Find essential information on drug interactions and other relevant details
  • Menadione crystalline 58-27-5 - MilliporeSigma
    Menadione is an aromatic polycyclic ketone It serves as a precursor for vitamin K synthesis Menadione is converted to menaquinone-4, an active metabolite of vitamin K3 Menadione mediates cell death, by inducing the production of reactive oxygen species through the futile redox cycling
  • Vitamin K3, Menadione, uses and toxicity - Health Jade
    Menadione (vitamin K3) is involved as a cofactor in the posttranslational gamma-carboxylation of glutamic acid residues of certain proteins in the body


















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