
Indole - Wikipedia
In the 1930s, interest in indole intensified when it became known that the indole substituent is present in many important alkaloids, known as indole alkaloids (e.g., tryptophan and auxins), …
Indole | Aromatic, Biosynthesis, Metabolism | Britannica
Indole, first isolated in 1866, has the molecular formula C 8 H 7 N, and it is commonly synthesized from phenylhydrazine and pyruvic acid, although several other procedures have been discovered.
What Is Indole Production and Why Is It Important?
Jun 24, 2025 · Indole is an aromatic, heterocyclic organic compound with a dual nature regarding its scent. In high concentrations, it has an intense fecal odor, yet in very dilute solutions, it …
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.
Indole - an overview | ScienceDirect Topics
Indole has enhanced the incidence of bladder cancer in some bioassays, for example, addition of indole to a diet containing 2-acetylaminofluorene produced an increased incidence of bladder …
Indole | C8H7N | CID 798 - PubChem
Indole is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).
Indole: Properties, Reactions, Production And Uses
Sep 5, 2024 · Indole, also known as 1-benzo [b]pyrrole, is an aromatic heterocyclic organic compound that has a bicyclic structure (a benzene fused to a pyrrole) with the chemical …
Indole Definition - Organic Chemistry Key Term | Fiveable
Indole is a heterocyclic aromatic organic compound composed of a benzene ring fused to a five-membered nitrogen-containing pyrrole ring. It is a key structural component found in various …
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 …
Indole = 99 120-72-9 - MilliporeSigma
Indole is a nitrogen-containing heterocycle used in the total synthesis of compounds such as goniomitine, [1] (−)-isatisine A, [2] and (±)-aspidospermidine. [3]