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Details

Stereochemistry RACEMIC
Molecular Formula C17H25NO
Molecular Weight 259.3865
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EPERISONE

SMILES

CCC1=CC=C(C=C1)C(=O)C(C)CN2CCCCC2

InChI

InChIKey=SQUNAWUMZGQQJD-UHFFFAOYSA-N
InChI=1S/C17H25NO/c1-3-15-7-9-16(10-8-15)17(19)14(2)13-18-11-5-4-6-12-18/h7-10,14H,3-6,11-13H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C17H25NO
Molecular Weight 259.3865
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:04:21 UTC 2023
Edited
by admin
on Fri Dec 15 16:04:21 UTC 2023
Record UNII
2M2P0551D3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EPERISONE
INN   MI   WHO-DD  
INN  
Official Name English
Eperisone [WHO-DD]
Common Name English
EPERISONE [MI]
Common Name English
1-(4-ETHYLPHENYL)-2-METHYL-3-(1-PIPERIDINYL)-1-PROPANONE
Systematic Name English
eperisone [INN]
Common Name English
EPERISONE [JAN]
Common Name English
4'-ETHYL-2-METHYL-3-PIPERIDINOPROPIOPHENONE
Systematic Name English
Classification Tree Code System Code
WHO-ATC M03BX09
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
WHO-VATC QM03BX09
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
NCI_THESAURUS C66880
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID5040671
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
WIKIPEDIA
EPERISONE
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
CAS
64840-90-0
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
MERCK INDEX
m4931
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY Merck Index
EVMPD
SUB06560MIG
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
DRUG CENTRAL
1022
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
PUBCHEM
3236
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
FDA UNII
2M2P0551D3
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
INN
5153
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
MESH
C030848
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
CHEBI
77069
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
SMS_ID
100000080244
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
ChEMBL
CHEMBL1902981
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
NCI_THESAURUS
C83692
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
DRUG BANK
DB08992
Created by admin on Fri Dec 15 16:04:21 UTC 2023 , Edited by admin on Fri Dec 15 16:04:21 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY