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Details

Stereochemistry RACEMIC
Molecular Formula C16H23NO
Molecular Weight 245.3599
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TOLPERISONE

SMILES

CC(CN1CCCCC1)C(=O)C2=CC=C(C)C=C2

InChI

InChIKey=FSKFPVLPFLJRQB-UHFFFAOYSA-N
InChI=1S/C16H23NO/c1-13-6-8-15(9-7-13)16(18)14(2)12-17-10-4-3-5-11-17/h6-9,14H,3-5,10-12H2,1-2H3

HIDE SMILES / InChI
Molecular Formula C16H23NO
Molecular Weight 245.3599
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:07:10 UTC 2023
Edited
by admin
on Fri Dec 15 16:07:10 UTC 2023
Record UNII
F5EOM0LD8E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TOLPERISONE
INN   MI   WHO-DD  
INN  
Official Name English
N-553 FREE BASE
Code English
2-METHYL-1-(4-METHYLPHENYL)-3-(1-PIPERIDINYL)-1-PROPANONE
Systematic Name English
2,4'-DIMETHYL-3-PIPERIDINOPROPIOPHENONE
Systematic Name English
TOLPERISONE [MI]
Common Name English
2-METHYL-3-PIPERIDINO-1-P-TOLYLPROPAN-1-ONE
Common Name English
NSC-107321
Code English
tolperisone [INN]
Common Name English
1-PIPERIDINO-2-METHYL-3-(P-TOLYL)-3-PROPANONE
Common Name English
Tolperisone [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29696
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
WHO-ATC M02AX06
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
WHO-VATC QM02AX06
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
WHO-VATC QM03BX04
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
WHO-ATC M03BX04
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
Code System Code Type Description
WIKIPEDIA
TOLPERISONE
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
DRUG CENTRAL
2703
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
ECHA (EC/EINECS)
211-976-4
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
SMS_ID
100000077763
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
NSC
107321
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
MESH
D014049
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
RXCUI
10639
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY RxNorm
CAS
728-88-1
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
MERCK INDEX
m10951
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID8023686
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
INN
3298
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
PUBCHEM
5511
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
FDA UNII
F5EOM0LD8E
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
DRUG BANK
DB06264
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
NCI_THESAURUS
C84219
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
EVMPD
SUB11173MIG
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
ChEMBL
CHEMBL1076211
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
Related Record Type Details
Structure of TOLPERISONE, (R)-
ENANTIOMER -> RACEMATE
Structure of TOLPERISONE HYDROCHLORIDE
SALT/SOLVATE -> PARENT
Structure of TOLPERISONE, (S)-
ENANTIOMER -> RACEMATE
Related Record Type Details
Structure of TOLPERISONE
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