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Details

Stereochemistry RACEMIC
Molecular Formula C19H15ClN2O4
Molecular Weight 370.786
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of REBAMIPIDE

SMILES

OC(=O)C(CC1=CC(=O)NC2=C1C=CC=C2)NC(=O)C3=CC=C(Cl)C=C3

InChI

InChIKey=ALLWOAVDORUJLA-UHFFFAOYSA-N
InChI=1S/C19H15ClN2O4/c20-13-7-5-11(6-8-13)18(24)22-16(19(25)26)9-12-10-17(23)21-15-4-2-1-3-14(12)15/h1-8,10,16H,9H2,(H,21,23)(H,22,24)(H,25,26)

HIDE SMILES / InChI
Molecular Formula C19H15ClN2O4
Molecular Weight 370.786
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 15:54:28 UTC 2023
Edited
by admin
on Fri Dec 15 15:54:28 UTC 2023
Record UNII
LR583V32ZR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
REBAMIPIDE
INN   JAN   MI   WHO-DD  
INN  
Official Name English
REBAMIPIDE [MI]
Common Name English
REBATOR
Brand Name English
(±)-.ALPHA.-(P-CHLOROBENZAMIDO)-1,2-DIHYDRO-2-OXO-4-QUINOLINEPROPIONIC ACID
Common Name English
NSC-758955
Code English
MUCOSTA
Brand Name English
PROAMIPIDE
Brand Name English
4-QUINOLINEPROPANOIC ACID, .ALPHA.-((4-CHLOROBENZOYL)AMINO)-1,2-DIHYDRO-2-OXO-
Systematic Name English
rebamipide [INN]
Common Name English
REBAMIPIDE [JAN]
Common Name English
OPC-12759
Code English
Rebamipide [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-ATC A02BX14
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
NCI_THESAURUS C29701
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
Code System Code Type Description
IUPHAR
871
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
FDA UNII
LR583V32ZR
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
CAS
90098-04-7
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
EPA CompTox
DTXSID8045937
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
NCI_THESAURUS
C29852
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
WIKIPEDIA
Rebamipide
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
EVMPD
SUB10267MIG
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
DRUG BANK
DB11656
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
MESH
C052785
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
DRUG CENTRAL
2360
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
PUBCHEM
5042
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
ChEMBL
CHEMBL1697771
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
MERCK INDEX
m9512
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY Merck Index
CAS
139344-42-6
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
SUPERSEDED
CAS
111911-87-6
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
SUPERSEDED
INN
6454
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
NSC
758955
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
SMS_ID
100000080803
Created by admin on Fri Dec 15 15:54:28 UTC 2023 , Edited by admin on Fri Dec 15 15:54:28 UTC 2023
PRIMARY
Related Record Type Details
Structure of REBAMIPIDE, (R)-
ENANTIOMER -> RACEMATE
Structure of REBAMIPIDE, (S)-
ENANTIOMER -> RACEMATE
Related Record Type Details
Structure of REBAMIPIDE MOFETIL
PARENT -> METABOLITE ACTIVE
Related Record Type Details
Structure of REBAMIPIDE
ACTIVE MOIETY
NIH
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