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Details

Stereochemistry RACEMIC
Molecular Formula C14H21NO4.ClH
Molecular Weight 303.782
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMBENOXAN HYDROCHLORIDE

SMILES

Cl.COCCOCCNCC1COC2=CC=CC=C2O1

InChI

InChIKey=DGDJOYSDXRNADN-UHFFFAOYSA-N
InChI=1S/C14H21NO4.ClH/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;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 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 Sat Dec 16 09:46:54 GMT 2023
Edited
by admin
on Sat Dec 16 09:46:54 GMT 2023
Record UNII
DHR4YM0G6V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMBENOXAN HYDROCHLORIDE
Common Name English
1,4-BENZODIOXIN-2-METHANAMINE, 2,3-DIHYDRO-N-(2-(2-METHOXYETHOXY)ETHYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
1,4-BENZODIOXAN-2-METHYLAMINE, N-(2-(2-METHOXYETHOXY)ETHYL)-, HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
PUBCHEM
15377
Created by admin on Sat Dec 16 09:46:54 GMT 2023 , Edited by admin on Sat Dec 16 09:46:54 GMT 2023
PRIMARY
FDA UNII
DHR4YM0G6V
Created by admin on Sat Dec 16 09:46:54 GMT 2023 , Edited by admin on Sat Dec 16 09:46:54 GMT 2023
PRIMARY
CAS
1617-99-8
Created by admin on Sat Dec 16 09:46:54 GMT 2023 , Edited by admin on Sat Dec 16 09:46:54 GMT 2023
PRIMARY
EPA CompTox
DTXSID70936589
Created by admin on Sat Dec 16 09:46:54 GMT 2023 , Edited by admin on Sat Dec 16 09:46:54 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY