Phenomorphan

Phenomorphan
Clinical data
Other names	(-)-3-hydroxy- N- (2-phenylethyl) morphinan
ATC code	none;
Legal status
Legal status	AU: S9 (Prohibited substance); BR: Class A1 (Narcotic drugs); CA: Schedule I ; DE: Anlage I (Authorized scientific use only); UK: Class A ; US: Schedule I ;
Identifiers
	IUPAC name 17-(2-Phenylethyl)morphinan-3-ol;
CAS Number	468-07-5 ;
PubChem CID	5362458 ;
ChemSpider	16735962 ;
UNII	26HXE4B73P ;
KEGG	D12688 ;
CompTox Dashboard (EPA)	DTXSID70878657 ;
ECHA InfoCard	100.006.732
Chemical and physical data
Formula	C24H29NO
Molar mass	347.502 g·mol−1
3D model (JSmol)	Interactive image ;
	SMILES Oc3ccc4C[C@H]1N(CC[C@@]2(CCCC[C@@H]12)c4c3)CCc5ccccc5;
	InChI InChI=1S/C24H29NO/c26-20-10-9-19-16-23-21-8-4-5-12-24(21,22(19)17-20)13-15-25(23)14-11-18-6-2-1-3-7-18/h1-3,6-7,9-10,17,21,23,26H,4-5,8,11-16H2/t21-,23+,24+/m0/s1 ; Key:CFBQYWXPZVQQTN-QPTUXGOLSA-N ;
	(verify)

Last updated June 30, 2025

Phenomorphan^[2] is an opioid analgesic. It is not currently used in medicine, but has similar side-effects to other opiates, which include itching, nausea and respiratory depression.

Phenomorphan is a highly potent drug due to the N-phenethyl group, which boosts affinity to the μ-opioid receptor, and so phenomorphan is around 10x more potent than levorphanol, which is itself 6-8x the potency of morphine. Other analogues where the N-(2-phenylethyl) group has been replaced by other aromatic rings^[3] are even more potent, with the N-(2-(2-furyl)ethyl) and the N-(2-(2-thienyl)ethyl) analogues being 60x and 45x stronger than levorphanol, respectively.^[4]

References

↑ 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 2023-08-16.
↑ USpatent 2885401,Grussner A, Hellerbach J, Schnider O,"Process for making morphinan derivatives and products available thereby",published 1956-03-22,issued 1959-05-05
↑ USpatent 2970147,Andre Grussner, Joseph Hellerbach, Otto Schnider,"3-hydroxy-N-(heterocyclic-ethyl)-morphinans",published 1958-11-26,issued 1961-01-31
↑ Hellerbach J, Schnider O, Besendorf H, Pellmont B (1966). Synthetic Analgesics: Part IIA. Morphinans. International series of monographs on organic chemistry. Pergamon Press.

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[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 2023-08-16.

[2] USpatent 2885401,Grussner A, Hellerbach J, Schnider O,"Process for making morphinan derivatives and products available thereby",published 1956-03-22,issued 1959-05-05

[3] USpatent 2970147,Andre Grussner, Joseph Hellerbach, Otto Schnider,"3-hydroxy-N-(heterocyclic-ethyl)-morphinans",published 1958-11-26,issued 1961-01-31

[4] Hellerbach J, Schnider O, Besendorf H, Pellmont B (1966). Synthetic Analgesics: Part IIA. Morphinans. International series of monographs on organic chemistry. Pergamon Press.

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Phenomorphan

See also

References