U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C14H21NO4
Molecular Weight 267.3208
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMBENOXAN

SMILES

COCCOCCNCC1COC2=C(O1)C=CC=C2

InChI

InChIKey=IRDXKUVPWPVZMA-UHFFFAOYSA-N
InChI=1S/C14H21NO4/c1-16-8-9-17-7-6-15-10-12-11-18-13-4-2-3-5-14(13)19-12/h2-5,12,15H,6-11H2,1H3

HIDE SMILES / InChI

Molecular Formula C14H21NO4
Molecular Weight 267.3208
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Ambenoxan is a muscle relaxant. Ambenoxan exerts its effects via an action on brain and/or spinal mechanisms. Ambenoxan has been shown to produce skeletal muscle flaccidity without loss of the righting reflex when administered orally or parenterally to rats, rabbits, dogs and monkeys. The drug is approximately twice as toxic orally as it is subcutaneously, which suggests that the compound is effectively absorbed by the oral route. Ambenoxan may be of value in the treatment of spastic disorders resulting from upper motor neurone damage in the brain or spinal cord, disseminated sclerosis, spastic diplegia and spastic hemiplegia.

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Wed Apr 02 09:24:20 GMT 2025
Edited
by admin
on Wed Apr 02 09:24:20 GMT 2025
Record UNII
YBP650462L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMBENOXAN
INN  
INN  
Official Name English
ambenoxan [INN]
Preferred Name English
N-(2-(2-METHOXYETHOXY)ETHYL)-1,4-BENZODIOXAN-2-METHYLAMINE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29696
Created by admin on Wed Apr 02 09:24:20 GMT 2025 , Edited by admin on Wed Apr 02 09:24:20 GMT 2025
Code System Code Type Description
INN
2635
Created by admin on Wed Apr 02 09:24:20 GMT 2025 , Edited by admin on Wed Apr 02 09:24:20 GMT 2025
PRIMARY
FDA UNII
YBP650462L
Created by admin on Wed Apr 02 09:24:20 GMT 2025 , Edited by admin on Wed Apr 02 09:24:20 GMT 2025
PRIMARY
EVMPD
SUB05395MIG
Created by admin on Wed Apr 02 09:24:20 GMT 2025 , Edited by admin on Wed Apr 02 09:24:20 GMT 2025
PRIMARY
NCI_THESAURUS
C73220
Created by admin on Wed Apr 02 09:24:20 GMT 2025 , Edited by admin on Wed Apr 02 09:24:20 GMT 2025
PRIMARY
EPA CompTox
DTXSID10862954
Created by admin on Wed Apr 02 09:24:20 GMT 2025 , Edited by admin on Wed Apr 02 09:24:20 GMT 2025
PRIMARY
ECHA (EC/EINECS)
219-531-6
Created by admin on Wed Apr 02 09:24:20 GMT 2025 , Edited by admin on Wed Apr 02 09:24:20 GMT 2025
PRIMARY
SMS_ID
100000087649
Created by admin on Wed Apr 02 09:24:20 GMT 2025 , Edited by admin on Wed Apr 02 09:24:20 GMT 2025
PRIMARY
CAS
2455-84-7
Created by admin on Wed Apr 02 09:24:20 GMT 2025 , Edited by admin on Wed Apr 02 09:24:20 GMT 2025
PRIMARY
ChEMBL
CHEMBL1742419
Created by admin on Wed Apr 02 09:24:20 GMT 2025 , Edited by admin on Wed Apr 02 09:24:20 GMT 2025
PRIMARY
PUBCHEM
15378
Created by admin on Wed Apr 02 09:24:20 GMT 2025 , Edited by admin on Wed Apr 02 09:24:20 GMT 2025
PRIMARY
MESH
C001076
Created by admin on Wed Apr 02 09:24:20 GMT 2025 , Edited by admin on Wed Apr 02 09:24:20 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY