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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
Structure of AMIXETRINE

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

HIDE SMILES / InChI

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

Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:23:48 GMT 2023
Edited
by admin
on Fri Dec 15 16:23:48 GMT 2023
Record UNII
7UL287YTPJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMIXETRINE
INN   MI  
INN  
Official Name English
amixetrine [INN]
Common Name English
PYRROLIDINE, 1-(2-(3-METHYLBUTOXY)-2-PHENYLETHYL)-
Systematic Name English
1-(.BETA.-(ISOPENTYLOXY)PHENETHYL)PYRROLIDINE
Systematic Name English
PYRROLIDINE, 1-(.BETA.-(ISOPENTYLOXY)PHENETHYL)-
Systematic Name English
AMIXETRINE [MI]
Common Name English
N-(2-PHENYL-2-ISOAMYLOXYETHYL)PYRROLIDINE
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
INN
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
MESH
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
EVMPD
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
MERCK INDEX
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
SMS_ID
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
DRUG CENTRAL
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
FDA UNII
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
WIKIPEDIA
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
ChEMBL
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
EPA CompTox
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
NCI_THESAURUS
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
PUBCHEM
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
CAS
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