MORPHINAN-3-OL, (±)-

Details

Stereochemistry	RACEMIC
Molecular Formula	C16H21NO
Molecular Weight	243.344
Optical Activity	( + / - )
Defined Stereocenters	3 / 3
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

[H][C@@]12CCCC[C@@]13CCN[C@@H]2CC4=CC=C(O)C=C34

InChI

InChIKey=IYNWSQDZXMGGGI-NUEKZKHPSA-N

InChI=1S/C16H21NO/c18-12-5-4-11-9-15-13-3-1-2-6-16(13,7-8-17-15)14(11)10-12/h4-5,10,13,15,17-18H,1-3,6-9H2/t13-,15+,16+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C16H21NO
Molecular Weight	243.344
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	3 / 3
E/Z Centers	0
Optical Activity	UNSPECIFIED

Description
Sources: https://apps.who.int/iris/bitstream/handle/10665/275695/WHO-EMP-RHT-TSN-2018.1-eng.pdf?sequence=1&isAllowed=y | https://www.drugfuture.com/chemdata/norlevorphanol.html | https://books.google.ru/books?id=4yaGePenGKgC&pg=PA469&lpg=PA469&dq=NORLEVORPHANOL retrieved from The A-Z Encyclopedia of Alcohol and Drug Abuse By Thomas Nordegren, p.469

Norlevorphanol is the levo-isomer of 3-hydroxymorphinan (morphinan-3-ol). It is is an opioid analgesic of the morphinan family. Norlevorphanol is a Schedule I controlled substance (opiate).

Approval Year

PubMed

Title	Date	PubMed
Influence of phenylalanine 120 on cytochrome P450 2D6 catalytic selectivity and regiospecificity: crucial role in 7-methoxy-4-(aminomethyl)-coumarin metabolism.	2004 Dec 1	15498516
3-hydroxymorphinan is neurotrophic to dopaminergic neurons and is also neuroprotective against LPS-induced neurotoxicity.	2005 Mar	15596482
Validation of a liquid chromatography-mass spectrometry method to assess the metabolism of dextromethorphan in rat everted gut sacs.	2005 May 5	15797528
Inhibitory effect of glutamate release from rat cerebrocortical synaptosomes by dextromethorphan and its metabolite 3-hydroxymorphinan.	2009 Jul	19428798
A validated SIM GC/MS method for the simultaneous determination of dextromethorphan and its metabolites dextrorphan, 3-methoxymorphinan and 3-hydroxymorphinan in biological matrices and its application to in vitro CYP2D6 and CYP3A4 inhibition study.	2009 Nov	19444798
Neuropsychotoxic and neuroprotective potentials of dextromethorphan and its analogs.	2011	21606622

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 17:36:17 GMT 2023` Edited by `admin` on `Sat Dec 16 17:36:17 GMT 2023`
Record UNII	E4S6LA88PG
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

MORPHINAN-3-OL, (±)-

Common Name

English

(±)-3-HYDROXYMORPHINAN

Common Name

English

Code System Code Type Description

WIKIPEDIA

3-Hydroxymorphinan

Created by admin on Sat Dec 16 17:36:17 GMT 2023 , Edited by admin on Sat Dec 16 17:36:17 GMT 2023

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FDA UNII

E4S6LA88PG

Created by admin on Sat Dec 16 17:36:17 GMT 2023 , Edited by admin on Sat Dec 16 17:36:17 GMT 2023

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PUBCHEM

5463854

Created by admin on Sat Dec 16 17:36:17 GMT 2023 , Edited by admin on Sat Dec 16 17:36:17 GMT 2023

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CAS

39131-41-4

Created by admin on Sat Dec 16 17:36:17 GMT 2023 , Edited by admin on Sat Dec 16 17:36:17 GMT 2023

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