Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H6ClNO3 |
Molecular Weight | 223.613 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=NC2=CC(Cl)=CC=C2C(O)=C1
InChI
InChIKey=UAWVRVFHMOSAPU-UHFFFAOYSA-N
InChI=1S/C10H6ClNO3/c11-5-1-2-6-7(3-5)12-8(10(14)15)4-9(6)13/h1-4H,(H,12,13)(H,14,15)
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2096911 Sources: https://www.ncbi.nlm.nih.gov/pubmed/2842779 |
0.56 µM [IC50] |
PubMed
Title | Date | PubMed |
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Glycine site antagonists abolish dopamine D2 but not D1 receptor mediated catalepsy in rats. | 1994 |
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Some central effects of kynurenic acid, 7-chlorokynurenic acid and 5,7- dichloro-kynurenic acid, glycine site antagonists. | 1994 May-Jun |
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Anticonvulsant efficacy of N-methyl-D-aspartate antagonists against convulsions induced by cocaine. | 1999 May |
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Prevention of cocaine-induced convulsions and lethality in mice: effectiveness of targeting different sites on the NMDA receptor complex. | 2000 Jan 28 |
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Role for D-serine within the ventral tegmental area in the development of cocaine's sensitization. | 2008 Apr |
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Code | English |
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18000-24-3
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1884
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DTXSID7042568
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149792
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C057013
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241-913-6
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7-Chlorokynurenic acid
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S7936QON2K
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ACTIVE MOIETY