Oxindole

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Oxindole
Skeletal formula
Ball-and-stick model
Names
Preferred IUPAC name
1,3-Dihydro-2H-indol-2-one
Identifiers
3D model (JSmol)
114692
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.000.390 Edit this at Wikidata
EC Number
  • 200-429-5
637057
KEGG
MeSH Oxindole
RTECS number
  • NM2080500
UNII
  • InChI=1S/C8H7NO/c10-8-5-6-3-1-2-4-7(6)9-8/h1-4H,5H2,(H,9,10) checkY
    Key: JYGFTBXVXVMTGB-UHFFFAOYSA-N checkY
  • c1ccc2c(c1)CC(=O)N2
Properties
C8H7NO
Molar mass 133.150 g·mol−1
Melting point 128 °C (262 °F; 401 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Oxindole (2-indolone) is an aromatic heterocyclic organic compound. It has a bicyclic structure, consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing ring. Oxindole is a modified indoline with a substituted carbonyl at the second position of the 5-member indoline ring.

Oxindole is a tryptophan derivative and in human biology is formed by gut bacteria ("normal flora"). It is normally metabolized and detoxified from the body by the liver. In excess, it can cause sedation, muscle weakness, hypotension, and coma. Patients with hepatic encephalopathy have been recorded to have elevated serum oxindole levels.[1]

Related aromatic compounds[]

References[]

  1. ^ Riggio, Oliviero; Mannaioni, Guido; Ridola, Lorenzo; Angeloni, Stefania; Merli, Manuela; Carlà, Vincenzo; Salvatori, Filippo Maria; Moroni, Flavio (2 February 2010). "Peripheral and Splanchnic Indole and Oxindole Levels in Cirrhotic Patients: A Study on the Pathophysiology of Hepatic Encephalopathy". The American Journal of Gastroenterology. 105 (6): 1374–1381. doi:10.1038/ajg.2009.738. PMID 20125128. S2CID 20633097.
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