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Details

Stereochemistry ACHIRAL
Molecular Formula C19H17ClN2O3
Molecular Weight 356.803
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LAQUINIMOD

SMILES

CCN(C(=O)C1=C(O)C2=C(C=CC=C2Cl)N(C)C1=O)C3=CC=CC=C3

InChI

InChIKey=GKWPCEFFIHSJOE-UHFFFAOYSA-N
InChI=1S/C19H17ClN2O3/c1-3-22(12-8-5-4-6-9-12)19(25)16-17(23)15-13(20)10-7-11-14(15)21(2)18(16)24/h4-11,23H,3H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C19H17ClN2O3
Molecular Weight 356.803
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 Sat Dec 16 17:39:21 UTC 2023
Edited
by admin
on Sat Dec 16 17:39:21 UTC 2023
Record UNII
908SY76S4G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LAQUINIMOD
INN   MI   WHO-DD  
INN  
Official Name English
TV-5600 FREE ACID
Code English
LAQUINIMOD [MI]
Common Name English
ABR-215062
Code English
Laquinimod [WHO-DD]
Common Name English
ABR-215062 FREE ACID
Code English
laquinimod [INN]
Common Name English
Classification Tree Code System Code
EMA ASSESSMENT REPORTS NERVENTRA (REFUSED: MULTIPLE SCLEROSIS)
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
WHO-VATC QN07XX10
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
NCI_THESAURUS C308
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
WHO-ATC N07XX10
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
Code System Code Type Description
MERCK INDEX
m6692
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY Merck Index
INN
8089
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
FDA UNII
908SY76S4G
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
EPA CompTox
DTXSID30179536
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
DRUG BANK
DB06685
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
WIKIPEDIA
LAQUINIMOD
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
CAS
248281-84-7
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
DRUG CENTRAL
4825
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
NCI_THESAURUS
C76569
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
ChEMBL
CHEMBL66092
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
SMS_ID
100000092997
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
PUBCHEM
54677946
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
EVMPD
SUB25236
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
MESH
C476223
Created by admin on Sat Dec 16 17:39:22 UTC 2023 , Edited by admin on Sat Dec 16 17:39:22 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> ACTIVATOR
SALT/SOLVATE -> PARENT
METABOLIC ENZYME -> SUBSTRATE
Related Record Type Details
ACTIVE MOIETY