Indole | Aromatic, Biosynthesis, Metabolism | Britannica
网页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.
A brief review of the biological potential of indole derivatives
网页2020年12月12日 · Indole-3-acetic acid is a plant hormone produced by the degradation of tryptophan in higher plants. Derivatives of indole are of wide interest because of their diverse biological and clinical applications. Here, we have tried to summarize the important pharmacological activity of indole derivatives [3].
Exploring the World of Indole: Synthesis, Chemistry and ... - Safrole
网页Indole is a versatile and significant heterocyclic compound that plays a crucial role in various fields, including pharmaceuticals and organic synthesis. Its synthesis can be achieved through several efficient methods, such as the Leimgruber-Batcho indole synthesis and the Fischer indole synthesis.
Indole - NIST Chemistry WebBook
网页In addition to the Thermodynamics Research Center (TRC) data available from this site, much more physical and chemical property data is available from the following TRC products: SRD 103a – Thermo Data Engine (TDE) for pure compounds.
Indole - NIST Chemistry WebBook
网页The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment.
Indole - NIST Chemistry WebBook
网页Indole. Formula: C 8 H 7 N. Molecular weight: 117.1479. IUPAC Standard InChI:InChI=1S/C8H7N/c1-2-4-8-7 (3-1)5-6-9-8/h1-6,9H Copy. IUPAC Standard InChIKey:SIKJAQJRHWYJAI-UHFFFAOYSA-N Copy. CAS Registry Number: 120-72-9.
Indole - an overview | ScienceDirect Topics
网页The interesting molecular architecture of indoles makes them suitable candidates for drug development. This chapter provides an overview of the chemistry, biology, and toxicology of indoles, focusing on their application as multitarget directed drugs.
Indole | C8H7N | CID 798 - PubChem
网页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. If released to the atmosphere, indole will mainly exist in the vapor phase based on a experimental vapor pressure of 0.0122 mm Hg at 25 °C.
Indole - an overview | ScienceDirect Topics
网页2011年2月3日 · Indole is a planar bicyclic molecule in which the benzene ring is fused through 2 and 3 positions of N-containing pyrrole ring. Indole, having 10 π-electrons (8 from double bonds and 2 from lone pair of electrons on nitrogen) is said to be aromatic in nature according to Huckel's rule.
Indoles and the advances in their biotechnological production for ...
网页2023年12月21日 · Indole is a signalling molecule produced both by bacteria and plants. In this review its signalling role between microbes and in particular in the human gut is discussed. Besides the natural roles, indole also has value for flavour and fragrance applications, for example, in food industry or perfumery.
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