Fenozolone

Group of stereoisomers
  • N06BA08 (WHO)
Identifiers
  • (RS)-2-ethylamino-5-phenyl-1,3-oxazol-4-one
CAS Number
  • 15302-16-6 checkY
PubChem CID
  • 71682
ChemSpider
  • 64736 checkY
UNII
  • 1NZI4LMU6G
KEGG
  • D07344 checkY
ChEBI
  • CHEBI:134865
ChEMBL
  • ChEMBL2104907
ECHA InfoCard100.035.747 Edit this at WikidataChemical and physical dataFormulaC11H12N2O2Molar mass204.229 g·mol−13D model (JSmol)
  • Interactive image
ChiralityRacemic mixture
  • O=C1\N=C(/OC1c2ccccc2)NCC
InChI
  • InChI=1S/C11H12N2O2/c1-2-12-11-13-10(14)9(15-11)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3,(H,12,13,14) checkY
  • Key:RXOIEVSUURELPG-UHFFFAOYSA-N checkY
  (verify)

Fenozolone (Ordinator) was developed by Laboratoires Dausse in the 1960s[1] and is a psychostimulant related to pemoline.[2]

See also

References

  1. ^ DE 1297108, Beil W, Hoeppener A, Wolff HJ, "5-phenyl-2-ethylamino-4-oxazolinone and its preparation", issued 12 June 1969, assigned to Les Laboratoires Dausse SA 
  2. ^ Gielsdorf W (February 1982). "Determination of the psychostimulants pemoline, fenozolone and thozalinone in human urine by gas chromatography/mass spectrometry and thin layer chromatography". Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift für klinische Chemie und klinische Biochemie. 20 (2): 65–8. doi:10.1515/cclm.1982.20.2.65. PMID 6121837. S2CID 38935748. Archived from the original on 2021-05-31. Retrieved 2021-05-31.
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AdamantanesAdenosine antagonistsAlkylaminesAmpakinesArylcyclohexylaminesBenzazepinesCathinonesCholinergicsConvulsantsEugeroicsOxazolinesPhenethylamines
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DRAsTooltip Dopamine releasing agents
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See also: Receptor/signaling modulators • Monoamine reuptake inhibitors • Adrenergics • Dopaminergics • Serotonergics • Monoamine metabolism modulators • Monoamine neurotoxins


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