Nicodicodine

Nicodicodine
Clinical data
Other names	Nicodicodeine, 6-Nicotinoyldihydrocodeine, Nicodicodina, Nicodicodinum
Routes of; administration	Oral, intravenous
ATC code	none;
Legal status
Legal status	AU: S2 (Pharmacy medicine); DE: Anlage II (Authorized trade only, not prescriptible); UK: Class B; UN: Narcotic Schedules I and III;
Identifiers
	IUPAC name (5alpha,6alpha)-3-Methoxy-17-methyl-4,5-epoxymorphinan-6-yl pyridine-3-carboxylate;
CAS Number	808-24-2;
PubChem CID	5464304;
ChemSpider	4576612;
UNII	04G0T06UGT;
CompTox Dashboard (EPA)	DTXSID40230642 ;
ECHA InfoCard	100.011.241
Chemical and physical data
Formula	C24H26N2O4
Molar mass	406.482 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CN1CCC23C4C1CC5=C2C(=C(C=C5)OC)OC3C(CC4)OC(=O)C6=CN=CC=C6;
	InChI InChI=InChI=1S/C24H26N2O4/c1-26-11-9-24-16-6-8-19(29-23(27)15-4-3-10-25-13-15)22(24)30-21-18(28-2)7-5-14(20(21)24)12-17(16)26/h3-5,7,10,13,16-17,19,22H,6,8-9,11-12H2,1-2H3/t16-,17+,19-,22-,24-/m0/s1; Key:GTGRMWCOZHEYRL-MJFIPZRTSA-N;
	(what is this?) (verify)

Nicodicodine is an opioid developed as a cough suppressant and analgesic.^[7] Synthesized in 1904, it is not commonly used, but has activity similar to other opioids.^[7] Nicodicodine is metabolised in the liver by demethylation to produce 6-nicotinoyldihydromorphine, and subsequently further metabolised to dihydromorphine. Since the final active metabolite is the slightly stronger opiate dihydromorphine rather than morphine, nicodicodine can be expected to be marginally more potent and longer acting than nicocodeine. Side effects are similar to those of other opioids and include itching, nausea and respiratory depression.

References

^ ^a ^b "Nicodicodine [INN:BAN:DCF] | SIELC". www.sielc.com. 16 May 2018. Retrieved 12 January 2019.
^ "Drugs Misuse Regulation 1987". www.legislation.qld.gov.au. Office of the Queensland Parliamentary Counsel. Retrieved 10 January 2019.
^ "Misuse of Drugs Act 1971". www.legislation.gov.uk. Retrieved 10 January 2019.
^ "The International Drug Control Conventions". undocs.org. United Nations. Retrieved 10 January 2019.
^ "Anlage II BtMG - Einzelnorm". www.gesetze-im-internet.de.
^ "Chemistry Dashboard". comptox.epa.gov. U.S. Environmental Protection Agency. Retrieved 10 January 2019.
^ ^a ^b Stolberg VB (2016). Painkillers: History, Science, and Issues. ABC-CLIO. p. 110. ISBN 978-1-4408-3532-2. Retrieved 12 January 2019.

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[SIELC-1] "Nicodicodine [INN:BAN:DCF] | SIELC". www.sielc.com. 16 May 2018. Retrieved 12 January 2019.

[2] "Drugs Misuse Regulation 1987". www.legislation.qld.gov.au. Office of the Queensland Parliamentary Counsel. Retrieved 10 January 2019.

[3] "Misuse of Drugs Act 1971". www.legislation.gov.uk. Retrieved 10 January 2019.

[4] "The International Drug Control Conventions". undocs.org. United Nations. Retrieved 10 January 2019.

[5] "Anlage II BtMG - Einzelnorm". www.gesetze-im-internet.de.

[6] "Chemistry Dashboard". comptox.epa.gov. U.S. Environmental Protection Agency. Retrieved 10 January 2019.

[Stolberb-7] Stolberg VB (2016). Painkillers: History, Science, and Issues. ABC-CLIO. p. 110. ISBN 978-1-4408-3532-2. Retrieved 12 January 2019.

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