Norcodeine

Chemical compound

Not to be confused with Norco (medication).

Pharmaceutical compound

Norcodeine
Clinical data

Dependence liability	High
ATC code	none
Legal status
Legal status	BR:Class A2 (Narcotic drugs)^[1] CA:Schedule I DE:Anlage I (Authorized scientific use only)
Identifiers
IUPAC name 3-Methoxy-6α-hydroxy-4,5α-epoxy-7,8-didehydromorphinan
CAS Number	467-15-2 ^{[画像:check]Y}
PubChem CID	9925873
ChemSpider	8101508 ^{[画像:X mark]N}
UNII	32W9P3T4ML
CompTox Dashboard (EPA)	DTXSID8046327 Edit this at Wikidata
ECHA InfoCard	100.006.718 Edit this at Wikidata
Chemical and physical data
Formula	C₁₇H₁₉NO₃
Molar mass	285.343g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES COC1=C2C3=C(C[C@@H]4[C@H]5[C@]3(CCN4)[C@@H](O2)[C@H](C=C5)O)C=C1
InChI InChI=1S/C17H19NO3/c1-20-13-5-2-9-8-11-10-3-4-12(19)16-17(10,6-7-18-11)14(9)15(13)21-16/h2-5,10-12,16,18-19H,6-8H2,1H3/t10-,11+,12-,16-,17-/m0/s1^{[画像:X mark]N} Key:HKOIXWVRNLGFOR-KOFBORESSA-N^{[画像:X mark]N}
^{[画像:X mark]N[画像:check]Y}(what is this?) (verify)

Norcodeine is an opiate analogue that is the N-demethylated derivative of codeine. It has relatively little opioid activity in its own right,^[2] but is formed as a metabolite of codeine following ingestion.^[3]

Norcodeine is a Schedule I Narcotic controlled substance in the US with the ACSCN of 9309 and zero annual manufacturing quota. The salts in use are the acetate (free base conversion ratio 0.826), hydroiodide (0.662), hydrochloride (0.759), nitrate (0.819), platinichloride (0.582), and sulphate (0.744).^[4]

References

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↑ Anvisa (2023年03月31日). "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年04月04日). Archived from the original on 2023年08月03日. Retrieved 2023年08月03日.
↑ Fraser HF, Isbell H, Vanhorn GD (June 1960). "Human pharmacology and addiction liability of norcodeine". The Journal of Pharmacology and Experimental Therapeutics. 129 (2): 172–7. doi:10.1016/S0022-3565(25)25805-0. PMID 13824628.
↑ Posey BL, Kimble SN (1984). "High-performance liquid chromatographic study of codeine, norcodeine, and morphine as indicators of codeine ingestion". Journal of Analytical Toxicology. 8 (2): 68–74. doi:10.1093/jat/8.2.68. PMID 6716978.
↑ "Quotas - 2014". DEA Diversion Control Division. Archived from the original on 2016年03月04日. Retrieved 2016年02月27日.