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=CC=CC=C2O1
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
Sat Dec 16 17:39:27 GMT 2023
by
admin
on
Sat Dec 16 17:39:27 GMT 2023
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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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-
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Common Name | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29696
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admin on Sat Dec 16 17:39:27 GMT 2023 , Edited by admin on Sat Dec 16 17:39:27 GMT 2023
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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
Created by
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100000087649
Created by
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2455-84-7
Created by
admin on Sat Dec 16 17:39:27 GMT 2023 , Edited by admin on Sat Dec 16 17:39:27 GMT 2023
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CHEMBL1742419
Created by
admin on Sat Dec 16 17:39:27 GMT 2023 , Edited by admin on Sat Dec 16 17:39:27 GMT 2023
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15378
Created by
admin on Sat Dec 16 17:39:27 GMT 2023 , Edited by admin on Sat Dec 16 17:39:27 GMT 2023
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C001076
Created by
admin on Sat Dec 16 17:39:27 GMT 2023 , Edited by admin on Sat Dec 16 17:39:27 GMT 2023
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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 |