Indole - Wikipedia Indole is an organic compound with the formula C 6 H 4 CCNH 3 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
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
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
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
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 - an overview | ScienceDirect Topics Presence of an indole nucleus in amino acid tryptophan makes it prominent in phytoconstituents such as perfumes, neurotransmitters, auxins (plant hormones), indole alkaloids, and so on The interesting molecular architecture of indoles makes them suitable candidates for drug development
Indoles - Chemistry Online Indole is a weak acid (with a value of pK a = 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: Chemical Properties, Synthesis, Applications, and Analysis In animals, indole is primarily produced in the gut microbiota, where it is generated as a byproduct of the breakdown of tryptophan, an essential amino acid This indole is involved in the regulation of intestinal health and contributes to the overall balance of the gut microbiome
Exploring the World of Indole: Synthesis, Chemistry and . . . - Safrole The name “indole” is a combination of the terms “indigo” and “oleum” since indole was first isolated by treating indigo dye with oleum The study of indole chemistry originated from the investigation of the dye indigo
Indole | Formula, Properties Application Indole is ubiquitous in nature and can be found in a wide variety of organisms Notably, it is a core component of the indole alkaloids, a class of compounds that includes some pharmaceuticals and plant defense molecules