Structure via PubChem · Public domain (PubChem)
carbostyril
Sign in to saveAlso known as 2(1H)-quinolinone, 2-quinolinone, 2-OXOQUINOLINE, 2-quinolone
2-Quinolone is an organic compound related structurally to quinoline. It is the majority tautomer in equilibrium with 2-quinolinol. The compound can be classified as a cyclic amide, and as such is used as an isostere for peptides and other pharmaceutically inspired targets. The 4-methyl-2-quinolone can be prepared by dehydration of acetoacetanilide.
In the Vinony graph
Vinony's link graph records 168 inbound references to carbostyril, and connects out to syphilis, meningitis and digital object identifier.
Vinony files it under 2-Quinolones, Chembox image size set and ECHA InfoCard ID from Wikidata.
Vinony links it to 4 Wikipedia language editions.
Chemical data
- Formula
- C9H7NO
- Molecular weight
- 145.16 g/mol
- IUPAC name
- 1H-quinolin-2-one
- SMILES
- C1=CC=C2C(=C1)C=CC(=O)N2
- InChIKey
- LISFMEBWQUVKPJ-UHFFFAOYSA-N
- XLogP
- 1.3
- Polar surface area
- 29.1 Ų
- H-bond donors
- 1
- H-bond acceptors
- 1
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Mass
- 145.053
Show 5 more facts
- chemical formula
- C₉H₇NO
- canonical SMILES
- C1=CC=C2C(=C1)C=CC(=O)N2
- melting point
- 198.0
- found in taxon
- Houttuynia cordata
- Commons category
- 2-Quinolone
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- References
- External links
2-Quinolone is an organic compound related structurally to quinoline. It is the majority tautomer in equilibrium with 2-quinolinol. The compound can be classified as a cyclic amide, and as such is used as an isostere for peptides and other pharmaceutically inspired targets. The 4-methyl-2-quinolone can be prepared by dehydration of acetoacetanilide.
thumb|left|2-Quinolone (right) and its tautomer 2-hydroxyquinoline (left)
Excerpted from Wikipedia’s “carbostyril” article, available under the CC BY-SA 4.0 licence.