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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H21N.ClH
Molecular Weight 263.806
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MORPHINAN HYDROCHLORIDE

SMILES

Cl.[H][C@@]12CC3=CC=CC=C3[C@]4(CCCC[C@@]14[H])CCN2

InChI

InChIKey=UTTZKIWMKFVYCK-CLUYDPBTSA-N
InChI=1S/C16H21N.ClH/c1-2-6-13-12(5-1)11-15-14-7-3-4-8-16(13,14)9-10-17-15;/h1-2,5-6,14-15,17H,3-4,7-11H2;1H/t14-,15+,16-;/m0./s1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C16H21N
Molecular Weight 227.3446
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Alkaloid biosynthesis in Papaver sp. cells in culture and during organogenesis.
2001 May-Jun
The stereocontrolled total synthesis of (-)-O-methylpallidinine.
2002 Dec 12
New dimeric morphine from opium poppy (Papaver somuniferum) and its physiological function.
2003 Jul
Electrospray tandem mass spectrometric investigations of morphinans.
2003 Nov
A new group of highly active analgesic of the morphinan family.
2004 Jan-Feb
Na+ modulation, inverse agonism, and anorectic potency of 4-phenylpiperidine opioid antagonists.
2004 Jun 28
Analysis of benzylisoquinoline-type alkaloids by electrospray tandem mass spectrometry and atmospheric pressure photoionization.
2005
Formic acid catalysed rearrangement of 5beta-methyldihydrothevinols (= 3,6-dimethoxy-5,17-dimethyl-4,5-epoxy-6,14-ethanomorphinan-7-methanols): synthesis of new doubly bridged morphinan derivatives.
2005 Feb
Morphinane alkaloids with cell protective effects from Sinomenium acutum.
2005 Jul
A plant-derived morphinan as a novel lead compound active against malaria liver stages.
2006 Dec
Persistence of evolutionary memory: primordial six-transmembrane helical domain mu opiate receptors selectively linked to endogenous morphine signaling.
2007 Dec
In-vitro investigation of oxazol and urea analogues of morphinan at opioid receptors.
2007 Jun 15
High-affinity carbamate analogues of morphinan at opioid receptors.
2007 Mar 15
Neuroprotective effects of cannabidiol in endotoxin-induced uveitis: critical role of p38 MAPK activation.
2008
Antidepressant-like effects of the novel kappa opioid antagonist MCL-144B in the forced-swim test.
2008
MLR-ANN and RTO approach to mu-opioid receptor-binding affinity. Pooling data from different sources.
2008 Mar
Synthesis of a stable iminium salt and propellane derivatives.
2008 Oct 17
Biochemistry and occurrence of o-demethylation in plant metabolism.
2010
Biological indications of a novel "short" µ opiate receptor in domestic chicken.
2010 Aug 30
Interactive effects of endogenous morphine, nitric oxide, and ethanol on mitochondrial processes.
2010 Oct
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:12:18 GMT 2023
Edited
by admin
on Sat Dec 16 01:12:18 GMT 2023
Record UNII
7Q4107D47X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MORPHINAN HYDROCHLORIDE
MI  
Systematic Name English
MORPHINAN HYDROCHLORIDE [MI]
Common Name English
(4AR,10R,10AR)-1,3,4,9,10,10A-HEXAHYDRO-2H-10,4A-(IMINOETHANO)PHENANTHRENE HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
PUBCHEM
20678913
Created by admin on Sat Dec 16 01:12:18 GMT 2023 , Edited by admin on Sat Dec 16 01:12:18 GMT 2023
PRIMARY
FDA UNII
7Q4107D47X
Created by admin on Sat Dec 16 01:12:18 GMT 2023 , Edited by admin on Sat Dec 16 01:12:18 GMT 2023
PRIMARY
MERCK INDEX
m7630
Created by admin on Sat Dec 16 01:12:18 GMT 2023 , Edited by admin on Sat Dec 16 01:12:18 GMT 2023
PRIMARY Merck Index
Related Record Type Details
PARENT -> SALT/SOLVATE
PARENT -> SALT/SOLVATE