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Details

Stereochemistry RACEMIC
Molecular Formula C20H23NO.ClH
Molecular Weight 329.864
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXAPROTILINE HYDROCHLORIDE

SMILES

Cl.CNCC(O)CC12CCC(C3=CC=CC=C13)C4=CC=CC=C24

InChI

InChIKey=MUOSVLIKDZRWMP-UHFFFAOYSA-N
InChI=1S/C20H23NO.ClH/c1-21-13-14(22)12-20-11-10-15(16-6-2-4-8-18(16)20)17-7-3-5-9-19(17)20;/h2-9,14-15,21-22H,10-13H2,1H3;1H

HIDE SMILES / InChI
Oxaprotiline (also known as hydroxymaprotiline) is a norepinephrine reuptake inhibitor and blocked the histamine H1 receptor. Oxaprotiline was studied in the treatment of hospitalized depressive patients. However, this drug has never been marketed.

Approval Year

PubMed

PubMed

TitleDatePubMed
Psychosocial determinants of recovery in depression.
2008
Modulation of electrically evoked serotonin release in cultured rat raphe neurons.
2007-03
PET imaging of norepinephrine transporters.
2006
Synthesis and C-11 labeling of three potent norepinephrine transporter selective ligands ((R)-nisoxetine, lortalamine, and oxaprotiline) for comparative PET studies in baboons.
2005-08-01
Comparative evaluation of positron emission tomography radiotracers for imaging the norepinephrine transporter: (S,S) and (R,R) enantiomers of reboxetine analogs ([11C]methylreboxetine, 3-Cl-[11C]methylreboxetine and [18F]fluororeboxetine), (R)-[11C]nisoxetine, [11C]oxaprotiline and [11C]lortalamine.
2005-07
Alpha2-adrenoceptors modulating neuronal serotonin release: a study in alpha2-adrenoceptor subtype-deficient mice.
2001-02
Differential effects of the enantiomers R(-) and S(+) oxaprotiline on major endogenous depression, the sleep EEG and neuroendocrine secretion: studies on depressed patients and normal controls.
1993-06
Oxaprotiline enantiomers given repeatedly and brain alpha-adrenoceptors.
1990
The influence of oxaprotiline enantiomers given repeatedly on the behavioural effects of d-amphetamine and dopamine injected into the nucleus accumbens.
1988-01-12
(+)-Oxaprotiline but not (-)-oxaprotiline given chronically potentiates the aggressive behaviour induced by clonidine.
1983-03
Patents
Name Type Language
OXAPROTILINE HYDROCHLORIDE
MART.   USAN   WHO-DD  
USAN  
Official Name English
NSC-310406
Preferred Name English
9,10-ETHANOANTHRACENE-9(10H)-ETHANOL, .ALPHA.-((METHYLAMINO)METHYL)-, HYDROCHLORIDE, (±)-
Systematic Name English
OXAPROTILINE HYDROCHLORIDE [MART.]
Common Name English
OXAPROTILINE HYDROCHLORIDE [USAN]
Common Name English
(±)-.ALPHA.-((METHYLAMINO)METHYL)-9,10-ETHANOANTHRACENE-9(10H)-ETHANOL HYDROCHLORIDE
Systematic Name English
C-49802B-BA
Code English
Oxaprotiline hydrochloride [WHO-DD]
Common Name English
Code System Code Type Description
NSC
310406
Created by admin on Mon Mar 31 19:17:52 GMT 2025 , Edited by admin on Mon Mar 31 19:17:52 GMT 2025
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NCI_THESAURUS
C175182
Created by admin on Mon Mar 31 19:17:52 GMT 2025 , Edited by admin on Mon Mar 31 19:17:52 GMT 2025
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SMS_ID
300000055562
Created by admin on Mon Mar 31 19:17:52 GMT 2025 , Edited by admin on Mon Mar 31 19:17:52 GMT 2025
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PUBCHEM
38206
Created by admin on Mon Mar 31 19:17:52 GMT 2025 , Edited by admin on Mon Mar 31 19:17:52 GMT 2025
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ChEMBL
CHEMBL2111067
Created by admin on Mon Mar 31 19:17:52 GMT 2025 , Edited by admin on Mon Mar 31 19:17:52 GMT 2025
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ECHA (EC/EINECS)
254-249-7
Created by admin on Mon Mar 31 19:17:52 GMT 2025 , Edited by admin on Mon Mar 31 19:17:52 GMT 2025
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FDA UNII
9DOW99I129
Created by admin on Mon Mar 31 19:17:52 GMT 2025 , Edited by admin on Mon Mar 31 19:17:52 GMT 2025
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CAS
39022-39-4
Created by admin on Mon Mar 31 19:17:52 GMT 2025 , Edited by admin on Mon Mar 31 19:17:52 GMT 2025
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