U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C10H5Cl2NO3
Molecular Weight 258.058
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5,7-DICHLOROKYNURENIC ACID

SMILES

OC(=O)C1=NC2=C(C(O)=C1)C(Cl)=CC(Cl)=C2

InChI

InChIKey=BGKFPRIGXAVYNX-UHFFFAOYSA-N
InChI=1S/C10H5Cl2NO3/c11-4-1-5(12)9-6(2-4)13-7(10(15)16)3-8(9)14/h1-3H,(H,13,14)(H,15,16)

HIDE SMILES / InChI

Molecular Formula C10H5Cl2NO3
Molecular Weight 258.058
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
68.0 nM [IC50]
PubMed

PubMed

TitleDatePubMed
Yohimbine-induced seizures involve NMDA and GABAergic transmission.
1992 Apr
Excitatory amino acid neurotransmission through both NMDA and non-NMDA receptors is involved in the anticonvulsant activity of felbamate in DBA/2 mice.
1994 Sep 1
Anticonvulsant activity of 5,7DCKA, NBQX, and felbamate against some chemoconvulsants in DBA/2 mice.
1996 Oct
The role of striatal glutamate receptors in models of Parkinson's disease.
1998
Contribution of the glycine site of NMDA receptors in rostral and intermediate-caudal parts of the striatum to the regulation of muscle tone in rats.
1998 May 18
Selective antagonism of rat inhibitory glycine receptor subunits.
2004 Feb 1
Model structures of the N-methyl-D-aspartate receptor subunit NR1 explain the molecular recognition of agonist and antagonist ligands.
2004 Mar
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:39:14 GMT 2023
Edited
by admin
on Fri Dec 15 19:39:14 GMT 2023
Record UNII
T61ORK73PY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5,7-DICHLOROKYNURENIC ACID
Common Name English
5,7-Dichloro-4-hydroxy-2-quinolinecarboxylic acid
Systematic Name English
2-Quinolinecarboxylic acid, 5,7-dichloro-4-hydroxy-
Systematic Name English
5,7-DCKA
Common Name English
Kynurenic acid, 5,7-dichloro-
Common Name English
Code System Code Type Description
WIKIPEDIA
5,7-Dichlorokynurenic acid
Created by admin on Fri Dec 15 19:39:14 GMT 2023 , Edited by admin on Fri Dec 15 19:39:14 GMT 2023
PRIMARY
MESH
C066192
Created by admin on Fri Dec 15 19:39:14 GMT 2023 , Edited by admin on Fri Dec 15 19:39:14 GMT 2023
PRIMARY
DRUG BANK
DB01931
Created by admin on Fri Dec 15 19:39:14 GMT 2023 , Edited by admin on Fri Dec 15 19:39:14 GMT 2023
PRIMARY
EPA CompTox
DTXSID80893710
Created by admin on Fri Dec 15 19:39:14 GMT 2023 , Edited by admin on Fri Dec 15 19:39:14 GMT 2023
PRIMARY
CAS
131123-76-7
Created by admin on Fri Dec 15 19:39:14 GMT 2023 , Edited by admin on Fri Dec 15 19:39:14 GMT 2023
PRIMARY
PUBCHEM
1779
Created by admin on Fri Dec 15 19:39:14 GMT 2023 , Edited by admin on Fri Dec 15 19:39:14 GMT 2023
PRIMARY
FDA UNII
T61ORK73PY
Created by admin on Fri Dec 15 19:39:14 GMT 2023 , Edited by admin on Fri Dec 15 19:39:14 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Binding assay
IC50