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
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
| 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
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:24:20 GMT 2025
by
admin
on
Wed Apr 02 09:24:20 GMT 2025
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| Record UNII |
YBP650462L
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| Record Status |
Validated (UNII)
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| Record Version |
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| Name | Type | Language | ||
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Official Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
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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
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| Code System | Code | Type | Description | ||
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2635
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YBP650462L
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SUB05395MIG
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C73220
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DTXSID10862954
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219-531-6
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100000087649
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2455-84-7
Created by
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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
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15378
Created by
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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
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |