Ethylmorphine

Source: Wikipedia, the free encyclopedia.
Ethylmorphine
Structural formula
Ball-and-stick model
Clinical data
Trade namesCosylan, Diolan, Dionina, Diosan, Solvipect, Trachyl
AHFS/Drugs.comInternational Drug Names
ATC code
Legal status
Legal status
  • BR: Class A2 (Narcotic drugs)[1]
  • CA: Schedule I
  • DE: Prescription only (
    Anlage II
    for higher doses)
  • UK: Class B
  • US: Schedule II and Schedule III (In Combination Products)
  • UN: Narcotic Schedule III
Identifiers
  • 7,8-didehydro-4,5-α-epoxy- 3-ethoxy-17-methylmorphinan-6-α-ol
JSmol)
  • O[C@H]2\C=C/[C@H]5[C@@H]4N(CC[C@@]51c3c(O[C@H]12)c(OCC)ccc3C4)C
  • InChI=1S/C19H23NO3/c1-3-22-15-7-4-11-10-13-12-5-6-14(21)18-19(12,8-9-20(13)2)16(11)17(15)23-18/h4-7,12-14,18,21H,3,8-10H2,1-2H3/t12-,13+,14-,18-,19-/m0/s1 checkY
  • Key:OGDVEMNWJVYAJL-LEPYJNQMSA-N checkY
  (verify)

Ethylmorphine (also known as codethyline, dionine, and ethyl morphine) is an

antitussive.[2][3][4][5][6][7]

Side effects

Adverse effects are similar to other

chemical dependence or addiction at high doses.[8]

Society and culture

Ethylmorphine was first marketed in France in 1953 by Houde, and in Norway and Spain in 1960. It is not available in the United States, where it is a Schedule II controlled substance.[8][9]

See also

References

  1. ^ Anvisa (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 2023-04-04). Archived from the original on 2023-08-03. Retrieved 2023-08-03.
  2. PMID 9140136
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  3. .
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  8. ^ .
  9. ^ PubChem. "Ethylmorphine". pubchem.ncbi.nlm.nih.gov. Retrieved 2023-09-08.