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Details

Stereochemistry ACHIRAL
Molecular Formula C9H17NO2
Molecular Weight 171.2368
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GABAPENTIN

SMILES

NCC1(CC(O)=O)CCCCC1

InChI

InChIKey=UGJMXCAKCUNAIE-UHFFFAOYSA-N
InChI=1S/C9H17NO2/c10-7-9(6-8(11)12)4-2-1-3-5-9/h1-7,10H2,(H,11,12)

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
GABAPENTIN
EP   HSDB   INN   JAN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
INN   USAN  
Official Name English
CYCLOHEXANEACETIC ACID, 1-(AMINOMETHYL)-
Common Name English
gabapentin [INN]
Common Name English
GABAPENTIN [ORANGE BOOK]
Common Name English
GRALISE
Brand Name English
GABAPENTIN [USP-RS]
Common Name English
1-(Aminomethyl)cyclohexaneacetic acid
Systematic Name English
Gabapentin [WHO-DD]
Common Name English
GABAPENTIN [MART.]
Common Name English
GABAPENTIN [MI]
Common Name English
GABAPENTIN [JAN]
Common Name English
NSC-742194
Code English
GABAPENTIN [EP IMPURITY]
Common Name English
NSC-759254
Code English
GABAPENTIN [USAN]
Common Name English
GABAPENTIN [HSDB]
Common Name English
GABAPENTIN [USP MONOGRAPH]
Common Name English
GABAPENTIN [VANDF]
Common Name English
GABAPENTIN [EP MONOGRAPH]
Common Name English
GOE 3450
Code English
DM-1796
Code English
CARBATIN
Systematic Name English
GOE-3450
Code English
GABAPENTINE
Common Name English
CI-945
Code English
Classification Tree Code System Code
WHO-VATC QN03AX12
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
WHO-ATC N03AX12
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
FDA ORPHAN DRUG 236506
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
NDF-RT N0000008486
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
NDF-RT N0000175753
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
FDA ORPHAN DRUG 88695
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
NCI_THESAURUS C29756
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
LIVERTOX NBK548252
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
Code System Code Type Description
USAN
AA-108
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
FDA UNII
6CW7F3G59X
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
MESH
C040029
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
SMS_ID
100000092663
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
MERCK INDEX
m5618
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY Merck Index
IUPHAR
5483
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
NCI_THESAURUS
C1108
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
CAS
60142-96-3
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
HSDB
7364
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
DAILYMED
6CW7F3G59X
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
ECHA (EC/EINECS)
262-076-3
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
DRUG BANK
DB00996
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
INN
5094
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
NSC
742194
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
EVMPD
SUB07857MIG
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
PUBCHEM
3446
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
RXCUI
25480
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY RxNorm
RS_ITEM_NUM
1287303
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
NSC
759254
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
CHEBI
42797
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
ChEMBL
CHEMBL940
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
LACTMED
Gabapentin
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
DRUG CENTRAL
1264
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
EPA CompTox
DTXSID0020074
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
WIKIPEDIA
GABAPENTIN
Created by admin on Fri Dec 15 15:06:57 UTC 2023 , Edited by admin on Fri Dec 15 15:06:57 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of GABAPENTIN
PRODRUG (METABOLITE ACTIVE)
Structure of GABAPENTIN ENACARBIL
SALT/SOLVATE (PARENT)
Structure of GABAPENTIN HYDROCHLORIDE
SALT/SOLVATE (PARENT)
Structure of GABAPENTIN HYDROBROMIDE
NIH
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