Indole is an organic compound with the formula C6H4CCNH3. Indole is classified as an aromatic heterocycle. It has a bicyclic structure, consisting of a...

The indole test is a biochemical test performed on bacterial species to determine the ability of the organism to convert tryptophan into indole. This...

Indole-3-carbinol (I3C, C9H9NO) is produced by the breakdown of the glucosinolate glucobrassicin, which can be found at relatively high levels in cruciferous...

Indole alkaloids are a class of alkaloids containing a structural moiety of indole; many indole alkaloids also include isoprene groups and are thus called...

Skatole or 3-methylindole is an organic compound belonging to the indole family. It occurs naturally in the feces of mammals and birds and is the primary...

of indole-3-carbinol, found in cruciferous vegetables, such as broccoli, Brussels sprouts, cabbage and kale. It and its parent compound – indole-3-carbinol...

The Fischer indole synthesis is a chemical reaction that produces the aromatic heterocycle indole from a (substituted) phenylhydrazine and an aldehyde...

Indole-3-acetic acid (IAA, 3-IAA) is the most common naturally occurring plant hormone of the auxin class. It is the best known of the auxins, and has...

with a very strong unpleasant odor. It has the chemical formula C9H9N. Indole Methyl 2-Methylindole (methylketol) 5-Methylindole 7-Methylindole Skatole...

Indole-3-butyric acid (1H-indole-3-butanoic acid, IBA) is a white to light-yellow crystalline solid, with the molecular formula C12H13NO2. It melts at...

The Larock indole synthesis is a heteroannulation reaction that uses palladium as a catalyst to synthesize indoles from an ortho-iodoaniline and a disubstituted...

5-Methylindole Names IUPAC name 5-Methyl-1H-indole Identifiers CAS Number 614-96-0 Y 3D model (JSmol) Interactive image Interactive image ChEMBL ChEMBL112462 Y...

production of agricultural chemicals and pharmaceuticals.[citation needed] Indole Methyl 1-Methylindole 2-Methylindole (methylketol) 5-Methylindole Skatole...

action of enzyme tryptophanase is converted to an Indole molecule, pyruvate and ammonium. The indole is then extracted from the broth by means of xylene...

In enzymology, an indole 2,3-dioxygenase (EC 1.13.11.17) is an enzyme that catalyzes the chemical reaction indole + O2 ⇌ {\displaystyle \rightleftharpoons...

7-Hydroxymitragynine (7-OH) is a terpenoid indole alkaloid from the plant Mitragyna speciosa, commonly known as kratom. It was first described in 1994...

Indole-3-acetaldehyde (IAL) belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists...

and 1.96% total indole content by dry weight. European fruiting bodies have been shown to have between 0.39% and 0.75% total indole content by dry weight...

Indole-3-carbaldehyde (I3A), also known as indole-3-aldehyde and 3-formylindole, is a metabolite of dietary L-tryptophan which is synthesized by human...

Indole-3-carboxylate decarboxylase (EC 4.1.1.92) is an enzyme with systematic name indole-3-carboxylate carboxy-lyase. This enzyme catalyses the following...

JWH-018 (1-pentyl-3-(1-naphthoyl)indole, NA-PIMO or AM-678) is an analgesic chemical from the naphthoylindole family that acts as a full agonist at both...

synthase (indole-salvaging) (EC 4.2.1.122, tryptophan synthase beta2) is an enzyme with systematic name L-serine hydro-lyase (adding indole, L-tryptophan-forming)...

Proteus vulgaris is a rod-shaped, nitrate-reducing, indole-positive and catalase-positive, hydrogen sulfide-producing, Gram-negative bacterium that inhabits...

for the diagnostical indole test, to determine the ability of the organism to split indole from the amino acid tryptophan. The indole produced yields a red...

naphthylmethylindoles, naphthoylpyrroles, naphthylmethylindenes, indole-3-carboxamides, indole-3-carboxylates, indazole-3-carboxamides and sometimes others...

synthesizing dyes, pigments, optical brighteners, and pharmaceuticals. Indole Methyl 1-Methylindole 5-Methylindole 7-Methylindole Skatole (3-methylindole)...

contains an α-amino group, an α-carboxylic acid group, and a side chain indole, making it a polar molecule with a non-polar aromatic beta carbon substituent...

The Hinsberg oxindole synthesis is a method of preparing oxindoles from the bisulfite additions of glyoxal. It is named after its inventor Oscar Hinsberg...

1-pentyl-3-(1-naphthoyl)indole (JWH-018) 1-butyl-3-(1-naphthoyl)indole (JWH-073) 1-pentyl-3-(4-methyl-1-naphthoyl)indole (JWH-122) 1-hexyl-3-(1-naphthoyl)indole (JWH-019)...

can be heated in the presence of strong acid to produce an indole via the Fischer indole synthesis. If there is a leaving group elsewhere in the Japp–Klingemann...