Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H27NO |
| Molecular Weight | 261.4024 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)CCOC(CN1CCCC1)C2=CC=CC=C2
InChI
InChIKey=ISRODTBNJUAWEJ-UHFFFAOYSA-N
InChI=1S/C17H27NO/c1-15(2)10-13-19-17(14-18-11-6-7-12-18)16-8-4-3-5-9-16/h3-5,8-9,15,17H,6-7,10-14H2,1-2H3
| Molecular Formula | C17H27NO |
| Molecular Weight | 261.4024 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Amixetrine is a drug that was formerly marketed in France but is now no longer sold. Amixetrine therapeutic functions are: aniinflammatory, anticholinergic, antidepressant, antispasmodic. The urinary metabolites of N-(2-phenyl-2-isoamyloxy) ethyl-pyrrolidine-hydrochloride (amixetrine) studied in man and in the dog demonstrated a comparable mode of transformation of the drugs for both species. In man, as in the dog, the principal metabolite coming from an omega-1-oxidation of the isoamyl chain corresponded to 2-phenyl-2-butoxy-(3-methyl-3-ol)ethyl-pyrrolidine.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:26:44 GMT 2025
by
admin
on
Mon Mar 31 18:26:44 GMT 2025
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| Record UNII |
7UL287YTPJ
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| Record Status |
Validated (UNII)
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| Record Version |
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C257
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admin on Mon Mar 31 18:26:44 GMT 2025 , Edited by admin on Mon Mar 31 18:26:44 GMT 2025
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| Code System | Code | Type | Description | ||
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3170
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C012181
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SUB05464MIG
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m36
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PRIMARY | Merck Index | ||
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100000087404
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3672
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7UL287YTPJ
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PRIMARY | |||
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Amixetrine
Created by
admin on Mon Mar 31 18:26:44 GMT 2025 , Edited by admin on Mon Mar 31 18:26:44 GMT 2025
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CHEMBL2104080
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DTXSID10865162
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C73072
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71911
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24622-72-8
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ENANTIOMER -> RACEMATE | |||
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PARENT -> SALT/SOLVATE | |||
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|
ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |