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Details

Stereochemistry RACEMIC
Molecular Formula C12H24N2O4
Molecular Weight 260.33
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARISOPRODOL

SMILES

CCCC(C)(COC(N)=O)COC(=O)NC(C)C

InChI

InChIKey=OFZCIYFFPZCNJE-UHFFFAOYSA-N
InChI=1S/C12H24N2O4/c1-5-6-12(4,7-17-10(13)15)8-18-11(16)14-9(2)3/h9H,5-8H2,1-4H3,(H2,13,15)(H,14,16)

HIDE SMILES / InChI
Molecular Formula C12H24N2O4
Molecular Weight 260.33
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 15:04:37 UTC 2023
Edited
by admin
on Fri Dec 15 15:04:37 UTC 2023
Record UNII
21925K482H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARISOPRODOL
EP   HSDB   INN   JAN   MART.   MI   ORANGE BOOK   USP   VANDF   WHO-DD  
INN  
Official Name English
(±)-2-METHYL-2-PROPYL-1,3-PROPANEDIOL CARBAMATE ISOPROPYLCARBAMATE
Systematic Name English
CARISOPRODOL [HSDB]
Common Name English
CARISOPRODOL COMPONENT OF CARISOPRODOL COMPOUND
Common Name English
CARISOPRODOL [USP MONOGRAPH]
Common Name English
NSC-172124
Code English
CARISOPRODOL [MI]
Common Name English
CARISOPRODOL [EP IMPURITY]
Common Name English
CARISOPRODOL [JAN]
Common Name English
carisoprodol [INN]
Common Name English
SOMA
Brand Name English
Carisoprodol [WHO-DD]
Common Name English
RELA
Brand Name English
CARISOPRODOL CIV
USP-RS  
Common Name English
CARISOPRODOL COMPONENT OF SOMA COMPOUND
Common Name English
SOMA COMPOUND COMPONENT CARISOPRODOL
Common Name English
CARISOPRODOL [VANDF]
Common Name English
CARISOPRODOL [ORANGE BOOK]
Common Name English
CARISOPRODOL CIV [USP-RS]
Common Name English
CARISOPRODOL COMPOUND COMPONENT CARISOPRODOL
Common Name English
CARISOPRODOL [MART.]
Common Name English
Classification Tree Code System Code
NDF-RT N0000175737
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
LIVERTOX NBK548829
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
WHO-ATC M03BA72
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
WHO-VATC QM03BA72
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
WHO-VATC QM03BA52
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
WHO-ATC M03BA02
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
NCI_THESAURUS C29696
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
WHO-VATC QM03BA02
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
DEA NO. 8192
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
WHO-ATC M03BA52
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
NDF-RT N0000175730
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C28904
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
PRIMARY
MESH
D002328
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
PRIMARY
SMS_ID
100000084595
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
PRIMARY
RS_ITEM_NUM
1096600
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
PRIMARY
WIKIPEDIA
CARISOPRODOL
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
PRIMARY
LACTMED
Carisoprodol
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
PRIMARY
FDA UNII
21925K482H
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
PRIMARY
DAILYMED
21925K482H
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
PRIMARY
CHEBI
3419
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
PRIMARY
IUPHAR
7610
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
PRIMARY
HSDB
3021
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
PRIMARY
DRUG BANK
DB00395
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
PRIMARY
EPA CompTox
DTXSID8024733
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
PRIMARY
PUBCHEM
2576
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
PRIMARY
NSC
172124
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
PRIMARY
CAS
78-44-4
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
PRIMARY
DRUG CENTRAL
509
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
PRIMARY
EVMPD
SUB06631MIG
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
PRIMARY
ECHA (EC/EINECS)
201-118-7
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
PRIMARY
MERCK INDEX
m3112
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
PRIMARY Merck Index
RXCUI
2101
Created by admin on Fri Dec 15 15:04:38 UTC 2023 , Edited by admin on Fri Dec 15 15:04:38 UTC 2023
PRIMARY RxNorm
INN
902
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
PRIMARY
ChEMBL
CHEMBL1233
Created by admin on Fri Dec 15 15:04:37 UTC 2023 , Edited by admin on Fri Dec 15 15:04:37 UTC 2023
PRIMARY
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Structure of CARISOPRODOL
BASIS OF STRENGTH->SUBSTANCE
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Structure of CARISOPRODOL, (R)-
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Structure of CARISOPRODOL, (S)-
ENANTIOMER -> RACEMATE
Structure of CARISOPRODOL
BASIS OF STRENGTH->SUBSTANCE
ASSAY (HPLC)
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PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
BINDING
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Structure of 2-(HYDROXYMETHYL)-2-METHYLPENTYL CARBAMATE
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Related Record Type Details
Structure of CARISOPRODOL
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC
NIH
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