Cloroqualone

Chemical compound
  • ?
Routes of
administration?ATC code
  • none
Pharmacokinetic dataBioavailability?Metabolism?Elimination half-life?Excretion?Identifiers
  • 3-(2,6-Dichlorophenyl)-2-ethyl-4-quinazolinone
CAS Number
  • 25509-07-3 ☒N
PubChem CID
  • 63338
DrugBank
  • ? ☒N
ChemSpider
  • 57005 checkY
UNII
  • 172D4Q6LOW
ChEMBL
  • ChEMBL2106114 ☒N
CompTox Dashboard (EPA)
  • DTXSID10180201 Edit this at Wikidata
ECHA InfoCard100.042.761 Edit this at WikidataChemical and physical dataFormulaC16H12Cl2N2OMolar mass319.19 g·mol−13D model (JSmol)
  • Interactive image
  • Clc3cccc(Cl)c3N/1C(=O)c2c(\N=C\1CC)cccc2
InChI
  • InChI=1S/C16H12Cl2N2O/c1-2-14-19-13-9-4-3-6-10(13)16(21)20(14)15-11(17)7-5-8-12(15)18/h3-9H,2H2,1H3 checkY
  • Key:SONHVLIDLXLSOL-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Cloroqualone is a quinazolinone-class GABAergic and is an analogue of methaqualone developed in the 1980s and marketed mainly in France and some other European countries. It has sedative and antitussive properties resulting from its agonist activity at the β subtype of the GABAa receptor and sigma-1 receptor, and was sold either alone or in combination with other ingredients as a cough medicine. Cloroqualone has weaker sedative properties than methaqualone and was sold for its useful cough-suppressing effects, but was withdrawn from the French market in 1994 because of concerns about its potential for abuse and overdose.[1][2][3]

See also

References

  1. ^ "Cloroqualone". PubChem. U.S. National Library of Medicine. Retrieved 2022-07-29.
  2. ^ Elks J (November 2014). The Dictionary of Drugs: Chemical Data. Springer US. p. 304. ISBN 978-1-4757-2085-3.
  3. ^ Martindale W, Reynolds JE (1993). Martindale: The Extra Pharmacopoeia (30th ed.). London: The Pharmaceutical Press. p. 745. ISBN 978-0-85369-300-0.
  • v
  • t
  • e
GABAA
Alcohols
Barbiturates
Benzodiazepines
Carbamates
Imidazoles
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Quinazolinones
Others
GABABH1
Antihistamines
Antidepressants
Antipsychotics
α2-Adrenergic5-HT2A
Antidepressants
Antipsychotics
Others
MelatoninOrexinα2δ VDCCOthers
  • v
  • t
  • e
GABAA receptor positive modulators
Alcohols
Barbiturates
Benzodiazepines
Carbamates
Flavonoids
Imidazoles
Kava constituents
  • 10-Methoxyyangonin
  • 11-Methoxyyangonin
  • 11-Hydroxyyangonin
  • Desmethoxyyangonin
  • 11-Methoxy-12-hydroxydehydrokavain
  • 7,8-Dihydroyangonin
  • Kavain
  • 5-Hydroxykavain
  • 5,6-Dihydroyangonin
  • 7,8-Dihydrokavain
  • 5,6,7,8-Tetrahydroyangonin
  • 5,6-Dehydromethysticin
  • Methysticin
  • 7,8-Dihydromethysticin
  • Yangonin
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Pyrazolopyridines
Quinazolinones
Volatiles/gases
Others/unsorted
  • Unsorted benzodiazepine site positive modulators: α-Pinene
  • MRK-409 (MK-0343)
  • TCS-1105
  • TCS-1205
See also: Receptor/signaling modulators • GABA receptor modulators • GABA metabolism/transport modulators


Stub icon

This sedative-related article is a stub. You can help Wikipedia by expanding it.

  • v
  • t
  • e