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Details

Stereochemistry RACEMIC
Molecular Formula C16H27NO6
Molecular Weight 329.3887
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GABAPENTIN ENACARBIL

SMILES

CC(C)C(=O)OC(C)OC(=O)NCC1(CC(O)=O)CCCCC1

InChI

InChIKey=TZDUHAJSIBHXDL-UHFFFAOYSA-N
InChI=1S/C16H27NO6/c1-11(2)14(20)22-12(3)23-15(21)17-10-16(9-13(18)19)7-5-4-6-8-16/h11-12H,4-10H2,1-3H3,(H,17,21)(H,18,19)

HIDE SMILES / InChI
Molecular Formula C16H27NO6
Molecular Weight 329.3887
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 15:50:03 UTC 2023
Edited
by admin
on Fri Dec 15 15:50:03 UTC 2023
Record UNII
75OCL1SPBQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GABAPENTIN ENACARBIL
DASH   INN   JAN   MART.   ORANGE BOOK   USAN   VANDF   WHO-DD  
USAN   INN  
Official Name English
GABAPENTIN ENACARBIL [MART.]
Common Name English
GSK1838262
Code English
gabapentin enacarbil [INN]
Common Name English
GSK-1838262
Code English
GABAPENTIN ENCARBIL [MI]
Common Name English
ASP8825
Code English
XP13512
Code English
CYCLOHEXANEACETIC ACID, 1-((((1-(2-METHYL-1-OXOPROPOXY)ETHOXY)CARBONYL)AMINO)METHYL)-
Common Name English
(1-{[({(1RS)-1-[(2-Methylpropanoyl)oxy]ethoxy}carbonyl)amino]methyl}cyclohexyl)acetic acid
Systematic Name English
GABAPENTIN ENACARBIL [ORANGE BOOK]
Common Name English
GABAPENTIN ENACARBIL [JAN]
Common Name English
ASP-8825
Code English
XP-13512
Code English
GABAPENTIN ENACARBIL [USAN]
Common Name English
HORIZANT
Brand Name English
Gabapentin Enacarbil [WHO-DD]
Common Name English
GABAPENTIN ENACARBIL [VANDF]
Common Name English
Classification Tree Code System Code
LIVERTOX NBK548415
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
NCI_THESAURUS C29756
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
FDA ORPHAN DRUG 330710
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
Code System Code Type Description
DRUG CENTRAL
4177
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
EVMPD
SUB35115
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
MERCK INDEX
m5619
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY Merck Index
INN
8611
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
EPA CompTox
DTXSID30870359
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
RXCUI
1101333
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY RxNorm
PUBCHEM
9883933
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
CAS
478296-72-9
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
SMS_ID
100000128276
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
IUPHAR
7560
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
CHEBI
68840
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
WIKIPEDIA
GABAPENTIN ENACARBIL
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
ChEMBL
CHEMBL1628502
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
DRUG BANK
DB08872
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
NCI_THESAURUS
C79579
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
FDA UNII
75OCL1SPBQ
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
DAILYMED
75OCL1SPBQ
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
USAN
UU-110
Created by admin on Fri Dec 15 15:50:03 UTC 2023 , Edited by admin on Fri Dec 15 15:50:03 UTC 2023
PRIMARY
Related Record Type Details
CYTOCHROME P450 2C9
METABOLIC ENZYME -> NON-SUBSTRATE
CYTOCHROME P450 3A4
METABOLIC ENZYME -> NON-SUBSTRATE
Structure of GABAPENTIN ENACARBIL, (S)-
ENANTIOMER -> RACEMATE
CYTOCHROME P450 2A6
METABOLIC ENZYME -> NON-SUBSTRATE
CYTOCHROME P450 2E1
METABOLIC ENZYME -> NON-SUBSTRATE
Structure of GABAPENTIN ENACARBIL
EXCRETED UNCHANGED
URINE
CYTOCHROME P450 2D6
METABOLIC ENZYME -> NON-SUBSTRATE
CYTOCHROME P450 2C19
METABOLIC ENZYME -> NON-SUBSTRATE
Structure of GABAPENTIN ENACARBIL, (R)-
ENANTIOMER -> RACEMATE
CYTOCHROME P450 1A2
METABOLIC ENZYME -> NON-SUBSTRATE
Related Record Type Details
Structure of GABAPENTIN
METABOLITE ACTIVE -> PRODRUG
Related Record Type Details
Structure of GABAPENTIN
ACTIVE MOIETY
NIH
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