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Details

Stereochemistry RACEMIC
Molecular Formula C11H15NO5
Molecular Weight 241.2405
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHOCARBAMOL

SMILES

COC1=C(OCC(O)COC(N)=O)C=CC=C1

InChI

InChIKey=GNXFOGHNGIVQEH-UHFFFAOYSA-N
InChI=1S/C11H15NO5/c1-15-9-4-2-3-5-10(9)16-6-8(13)7-17-11(12)14/h2-5,8,13H,6-7H2,1H3,(H2,12,14)

HIDE SMILES / InChI
Molecular Formula C11H15NO5
Molecular Weight 241.2405
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 15:03:13 UTC 2023
Edited
by admin
on Fri Dec 15 15:03:13 UTC 2023
Record UNII
125OD7737X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHOCARBAMOL
GREEN BOOK   HSDB   INN   JAN   MART.   MI   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD  
INN  
Official Name English
ROBAXISAL COMPONENT METHOCARBAMOL
Common Name English
1,2-PROPANEDIOL, 3-(2-METHOXYPHENOXY)-, 1-CARBAMATE, (±)-
Common Name English
NSC-170960
Code English
(±)-3-(O-METHOXYPHENOXY)-1,2-PROPANEDIOL 1-CARBAMATE
Common Name English
DELAXIN
Brand Name English
METHOCARBAMOL [MART.]
Common Name English
ROBAXIN
Brand Name English
FORBAXIN
Brand Name English
METHOCARBAMOL [MI]
Common Name English
methocarbamol [INN]
Common Name English
METHOCARBAMOL [VANDF]
Common Name English
METHOCARBAMOL [ORANGE BOOK]
Common Name English
METHOCARBAMOL [JAN]
Common Name English
METHOCARBAMOL [USP MONOGRAPH]
Common Name English
METHOCARBAMOL COMPONENT OF ROBAXISAL
Common Name English
Methocarbamol [WHO-DD]
Common Name English
METHOCARBAMOL [GREEN BOOK]
Common Name English
METHOCARBAMOL [USP-RS]
Common Name English
METHOCARBAMOL [HSDB]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29696
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
CFR 21 CFR 522.1380
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
WHO-VATC QM03BA53
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
WHO-VATC QM03BA73
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
NDF-RT N0000175737
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
WHO-ATC M03BA03
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
WHO-VATC QM03BA03
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
LIVERTOX NBK548286
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
WHO-ATC M03BA53
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
CFR 21 CFR 520.1380
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
WHO-ATC M03BA73
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
NDF-RT N0000175730
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
Code System Code Type Description
FDA UNII
125OD7737X
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
MERCK INDEX
m7322
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY Merck Index
IUPHAR
6829
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
CAS
532-03-6
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
EPA CompTox
DTXSID6023286
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
INN
776
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
DRUG CENTRAL
1747
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
PUBCHEM
4107
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
DAILYMED
125OD7737X
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
RS_ITEM_NUM
1412008
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
EVMPD
SUB08852MIG
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
WIKIPEDIA
METHOCARBAMOL
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
ChEMBL
CHEMBL1201117
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
ECHA (EC/EINECS)
208-524-3
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
DRUG BANK
DB00423
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
RXCUI
6845
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY RxNorm
MESH
D008721
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
NCI_THESAURUS
C29252
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
SMS_ID
100000081453
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
CHEBI
6832
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
NSC
170960
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
HSDB
3122
Created by admin on Fri Dec 15 15:03:13 UTC 2023 , Edited by admin on Fri Dec 15 15:03:13 UTC 2023
PRIMARY
Related Record Type Details
Structure of 3-(2-HYDROXYPHENOXY)-1,2-PROPANEDIOL 1-CARBAMATE
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Structure of GUAIFENESIN
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
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Related Record Type Details
Structure of METHOCARBAMOL
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC Elimination
PHARMACOKINETIC
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
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