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Details

Stereochemistry ACHIRAL
Molecular Formula C11H14N2O4
Molecular Weight 238.2399
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FELBAMATE

SMILES

NC(=O)OCC(COC(N)=O)C1=CC=CC=C1

InChI

InChIKey=WKGXYQFOCVYPAC-UHFFFAOYSA-N
InChI=1S/C11H14N2O4/c12-10(14)16-6-9(7-17-11(13)15)8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H2,12,14)(H2,13,15)

HIDE SMILES / InChI
Molecular Formula C11H14N2O4
Molecular Weight 238.2399
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:16:48 UTC 2023
Edited
by admin
on Fri Dec 15 15:16:48 UTC 2023
Record UNII
X72RBB02N8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FELBAMATE
HSDB   INN   MART.   MI   ORANGE BOOK   USAN   USP-RS   VANDF   WHO-DD  
INN   USAN  
Official Name English
ADD-03055
Code English
W-554
Code English
FELBAMATE [ORANGE BOOK]
Common Name English
FELBAMATE [USP MONOGRAPH]
Common Name English
Felbamate [WHO-DD]
Common Name English
CARBAMIC ACID 2-PHENYLTRIMETHYLENE ESTER
Common Name English
FELBAMATE [MI]
Common Name English
2-Phenyl-1,3-propanediol dicarbamate
Systematic Name English
FELBAMATE [USP-RS]
Common Name English
2-PHENYL-1,3-PROPANEDIOL 1,3-DICARBAMATE
Common Name English
felbamate [INN]
Common Name English
1,3-PROPANEDIOL, 2-PHENYL-, DICARBAMATE
Systematic Name English
FELBATOL
Brand Name English
FELBAMATE [VANDF]
Common Name English
FELBAMATE [USAN]
Common Name English
FELBAMATE [MART.]
Common Name English
TALOXA
Brand Name English
FELBAMATE [HSDB]
Common Name English
NSC-759866
Code English
Classification Tree Code System Code
LIVERTOX NBK548256
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
NCI_THESAURUS C264
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
NDF-RT N0000008486
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
NDF-RT N0000175753
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
FDA ORPHAN DRUG 33488
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
WHO-ATC N03AX10
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
WHO-VATC QN03AX10
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
Code System Code Type Description
RS_ITEM_NUM
1269312
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
SMS_ID
100000081237
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
RXCUI
24812
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY RxNorm
MESH
C047360
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
NCI_THESAURUS
C47530
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
EPA CompTox
DTXSID9023041
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
IUPHAR
5473
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
EVMPD
SUB07526MIG
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
CAS
25451-15-4
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
HSDB
7525
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
FDA UNII
X72RBB02N8
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
DAILYMED
X72RBB02N8
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
WIKIPEDIA
FELBAMATE
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
DRUG BANK
DB00949
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
USAN
W-17
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
CHEBI
4995
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
MERCK INDEX
m5254
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY Merck Index
LACTMED
Felbamate
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
PUBCHEM
3331
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
INN
5686
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
DRUG CENTRAL
1140
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
ECHA (EC/EINECS)
247-001-4
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
NSC
759866
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
ChEMBL
CHEMBL1094
Created by admin on Fri Dec 15 15:16:48 UTC 2023 , Edited by admin on Fri Dec 15 15:16:48 UTC 2023
PRIMARY
Related Record Type Details
PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
BINDING
Structure of FELBAMATE
BASIS OF STRENGTH->SUBSTANCE
ASSAY (HPLC)
USP
Related Record Type Details
Structure of CMBA DERIVATIVE
METABOLITE -> PARENT
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METABOLITE -> PARENT
Structure of 3-CARBAMOYL-2-PHENYL-PROPIONALDEHYDE
METABOLITE -> PARENT
Related Record Type Details
Structure of N-AMINOCARBONYL FELBAMATE
IMPURITY -> PARENT
Relative Response Factor 0.89
CHROMATOGRAPHIC PURITY (HPLC/UV)
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Structure of 3-HYDROXY-2-PHENYLPROPYL CARBAMATE
IMPURITY -> PARENT
Relative Response Factor 1.3
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of PHENYLPROPANEDIOL
IMPURITY -> PARENT
Relative Response Factor 1.7
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of PHENETHYL CARBAMATE
IMPURITY -> PARENT
Relative Response Factor 1.29
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Related Record Type Details
Structure of FELBAMATE
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Volume of Distribution PHARMACOKINETIC
Biological Half-life PHARMACOKINETIC
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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