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
Fri Dec 15 16:23:48 GMT 2023
by
admin
on
Fri Dec 15 16:23:48 GMT 2023
|
Record UNII |
7UL287YTPJ
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C257
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
3170
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY | |||
|
C012181
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY | |||
|
SUB05464MIG
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY | |||
|
m36
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY | Merck Index | ||
|
100000087404
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY | |||
|
3672
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY | |||
|
7UL287YTPJ
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY | |||
|
Amixetrine
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY | |||
|
CHEMBL2104080
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY | |||
|
DTXSID10865162
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY | |||
|
C73072
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY | |||
|
71911
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY | |||
|
24622-72-8
Created by
admin on Fri Dec 15 16:23:48 GMT 2023 , Edited by admin on Fri Dec 15 16:23:48 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ENANTIOMER -> RACEMATE | |||
|
PARENT -> SALT/SOLVATE | |||
|
ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |