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Details

Stereochemistry RACEMIC
Molecular Formula C18H21N3O3S
Molecular Weight 359.443
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RABEPRAZOLE

SMILES

COCCCOC1=CC=NC(C[S+]([O-])C2=NC3=C(N2)C=CC=C3)=C1C

InChI

InChIKey=YREYEVIYCVEVJK-UHFFFAOYSA-N
InChI=1S/C18H21N3O3S/c1-13-16(19-9-8-17(13)24-11-5-10-23-2)12-25(22)18-20-14-6-3-4-7-15(14)21-18/h3-4,6-9H,5,10-12H2,1-2H3,(H,20,21)

HIDE SMILES / InChI

Molecular Formula C18H21N3O3S
Molecular Weight 359.443
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:44:20 UTC 2023
Edited
by admin
on Fri Dec 15 15:44:20 UTC 2023
Record UNII
32828355LL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RABEPRAZOLE
HSDB   INN   MI   VANDF   WHO-DD  
INN  
Official Name English
LY-307640
Code English
E-3810 (PPI)
Code English
1H-BENZIMIDAZOLE, 2-(((4-(3-METHOXYPROPOXY)-3-METHYL-2-PYRIDINYL)METHYL)SULFINYL)-
Systematic Name English
E3810
Code English
rabeprazole [INN]
Common Name English
LY307640
Code English
RABEPRAZOLE [VANDF]
Common Name English
RABEPRAZOLE [MI]
Common Name English
PARIPRAZOLE
Common Name English
Rabeprazole [WHO-DD]
Common Name English
ERALOC
Brand Name English
RABEPRAZOLE [HSDB]
Common Name English
Classification Tree Code System Code
NDF-RT N0000175525
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
LIVERTOX NBK548154
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
WHO-ATC A02BC54
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
NDF-RT N0000000147
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
WHO-ATC A02BC04
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
WHO-VATC QA02BC04
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
NCI_THESAURUS C29723
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
Code System Code Type Description
EVMPD
SUB10229MIG
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
EPA CompTox
DTXSID3044122
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
INN
7112
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
SMS_ID
100000080304
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
LACTMED
Rabeprazole
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
IUPHAR
7290
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
MESH
C063129
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
DRUG BANK
DB01129
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
WIKIPEDIA
RABEPRAZOLE
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
CHEBI
8768
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
CAS
117976-89-3
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
PUBCHEM
5029
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
HSDB
7321
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
MERCK INDEX
m9476
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY Merck Index
NCI_THESAURUS
C29410
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
RXCUI
114979
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY RxNorm
DAILYMED
32828355LL
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
DRUG CENTRAL
2350
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
ChEMBL
CHEMBL1219
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
FDA UNII
32828355LL
Created by admin on Fri Dec 15 15:44:20 UTC 2023 , Edited by admin on Fri Dec 15 15:44:20 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
BINDER->LIGAND
BINDING
TARGET -> INHIBITOR
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
Related Record Type Details
METABOLITE -> PARENT
MAJOR
METABOLITE ACTIVE -> PARENT
METABOLITE ACTIVE -> PRODRUG
METABOLITE -> PARENT
METABOLITE ACTIVE -> PARENT
reduced mainly via a non-enzymatic pathway to thioether-rabeprazole (thioether-RPZ), with only minor CYP2C19 and CYP3A4 involvement
MAJOR
METABOLITE ACTIVE -> PRODRUG
Related Record Type Details
IMPURITY -> PARENT
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC