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indole    
n. 吲哚

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  • Indole - Wikipedia
    Indole Indole is an organic compound with the formula C6H4CCNH3 Indole is classified as an aromatic heterocycle It has a bicyclic structure, consisting of a six-membered benzene ring fused to a five-membered pyrrole ring Indoles are derivatives of indole where one or more of the hydrogen atoms have been replaced by substituent groups
  • Indole | C8H7N | CID 798 - PubChem
    Indole | C8H7N | CID 798 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety hazards toxicity information, supplier lists, and more
  • Biomedical Importance of Indoles - PMC
    The indole nucleus is an important element of many natural and synthetic molecules with significant biological activity This review covers some of the relevant and recent achievements in the biological, chemical and pharmacological activity of
  • Indole | Aromatic, Biosynthesis, Metabolism | Britannica
    indole, a heterocyclic organic compound occurring in some flower oils, such as jasmine and orange blossom, in coal tar, and in fecal matter It is used in perfumery and in making tryptophan, an essential amino acid, and indoleacetic acid (heteroauxin), a hormone that promotes the development of roots in plant cuttings
  • Indole - Simple English Wikipedia, the free encyclopedia
    Indole Indole (a blending of the terms indigo and oleum) is an organic compound The chemical can be found in many places in nature It can be produced by bacteria At room temperature, indole is a solid Indole is found in some vegetables They include broccoli, cauliflower and cabbage [2] It is also in human feces It has a strong fecal
  • What Is Indole Production and Why Is It Important?
    Discover indole, a molecule derived from tryptophan that acts as a critical messenger It helps regulate microbial communities and has complex effects on host physiology
  • Indoles - Chemistry Online
    Indole is a weak acid (with a value of pKa = 16 97), with an acidity comparable to pyrrole, and to aliphatic alcohols It can be converted to the N -sodium derivative, in liquid ammonia, or with sodium hydride (NaH) in an organic solvent
  • Indole - an overview | ScienceDirect Topics
    Indole's production and use as a chemical intermediate, a perfume fixative, a synthetic flavor, and possibly a kairomone may result in its release to the environment through various waste streams Indole is released directly to the environment as a component of tobacco smoke and occurs naturally in coal tar, jasmine oil and orange-blossom oil
  • Indole: Chemical Properties, Synthesis, Applications, and Analysis
    Learn about indole, its chemical properties, synthesis methods, biological role, applications in industry, and key analysis techniques used in research and industry
  • Why Foods High in Indoles May Be Good for Your Health
    Specific indole molecules (derived in the gut from the breakdown of the glucobrassicin in cruciferous vegetables) that have shown estrogen-reducing effects in preclinical (animal and laboratory) studies are indole-3-carbinol (I3C) and 3,3'-diindolylmethane (DIM), according to the Micronutrient Information Center at Oregon State University (OSU)





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