OXAPROTILINE HYDROCHLORIDE

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 Search

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

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	C20H23NO
Molecular Weight	293.4027
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3527706 | https://www.ncbi.nlm.nih.gov/pubmed/1353628

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.

CNS Activity

Approval Year

PubMed

Title	Date	PubMed
(+)-Oxaprotiline but not (-)-oxaprotiline given chronically potentiates the aggressive behaviour induced by clonidine.	1983 Mar	6132979
The influence of oxaprotiline enantiomers given repeatedly on the behavioural effects of d-amphetamine and dopamine injected into the nucleus accumbens.	1988 Jan 12	3350045
Oxaprotiline enantiomers given repeatedly and brain alpha-adrenoceptors.	1990	2158798
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 Jun	8364347
Alpha2-adrenoceptors modulating neuronal serotonin release: a study in alpha2-adrenoceptor subtype-deficient mice.	2001 Feb	11181434
Synthesis and C-11 labeling of three potent norepinephrine transporter selective ligands ((R)-nisoxetine, lortalamine, and oxaprotiline) for comparative PET studies in baboons.	2005 Aug 1	15914010
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 Jul	15998285
Modulation of electrically evoked serotonin release in cultured rat raphe neurons.	2007 Mar	17348865
Psychosocial determinants of recovery in depression.	2008	19170403

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 18:38:42 UTC 2023` Edited by `admin` on `Fri Dec 15 18:38:42 UTC 2023`
Record UNII	9DOW99I129
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

OXAPROTILINE HYDROCHLORIDE

Official 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

NSC-310406

Code

English

C-49802B-BA

Code

English

Oxaprotiline hydrochloride [WHO-DD]

Common Name

English

Code System Code Type Description

NSC

310406