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Found 33 with Last Name = 'kvist' and Initial = 't'
TargetGlutamate receptor ionotropic, NMDA 2A(Rattus norvegicus (Rat))
University of Copenhagen

LigandPNGBDBM213889(5,7-Dichlorokynurenic acid (5,7-DCKA))
Affinity DataKi:  65nM ΔG°:  -41.0kJ/mole IC50:  92nMpH: 7.4 T: 2°CAssay Description:Two-electrode voltage clamp (TEVC) recordings were performed on Xenopus oocytes at room temperature 3-6 days postinjection using an OC-725C TEVC ampl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, NMDA 2D(Rattus norvegicus (Rat))
University of Copenhagen

LigandPNGBDBM213888(1-thioxo-1,2-dihydro-[1,2,4]triazolo[4,3-a]-quinox...)
Affinity DataKi: >300nM ΔG°: >-37.2kJ/mole IC50: >3.00E+3nMpH: 7.4 T: 2°CAssay Description:Two-electrode voltage clamp (TEVC) recordings were performed on Xenopus oocytes at room temperature 3-6 days postinjection using an OC-725C TEVC ampl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, NMDA 2A(Rattus norvegicus (Rat))
University of Copenhagen

LigandPNGBDBM213888(1-thioxo-1,2-dihydro-[1,2,4]triazolo[4,3-a]-quinox...)
Affinity DataKi:  560nM ΔG°:  -35.7kJ/mole IC50:  770nMpH: 7.4 T: 2°CAssay Description:Two-electrode voltage clamp (TEVC) recordings were performed on Xenopus oocytes at room temperature 3-6 days postinjection using an OC-725C TEVC ampl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, NMDA 2C(Rattus norvegicus (Rat))
University of Copenhagen

LigandPNGBDBM213888(1-thioxo-1,2-dihydro-[1,2,4]triazolo[4,3-a]-quinox...)
Affinity DataKi: >800nM ΔG°: >-34.8kJ/mole IC50: >3.00E+3nMpH: 7.4 T: 2°CAssay Description:Two-electrode voltage clamp (TEVC) recordings were performed on Xenopus oocytes at room temperature 3-6 days postinjection using an OC-725C TEVC ampl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, NMDA 2B(Rattus norvegicus (Rat))
University of Copenhagen

LigandPNGBDBM213888(1-thioxo-1,2-dihydro-[1,2,4]triazolo[4,3-a]-quinox...)
Affinity DataKi: >1.30E+3nM ΔG°: >-33.6kJ/mole IC50: >3.00E+3nMpH: 7.4 T: 2°CAssay Description:Two-electrode voltage clamp (TEVC) recordings were performed on Xenopus oocytes at room temperature 3-6 days postinjection using an OC-725C TEVC ampl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-aminobutyrate aminotransferase, mitochondrial(Rattus norvegicus)
Northwestern University

Curated by ChEMBL
LigandPNGBDBM50401019(CHEMBL2203661)
Affinity DataKi:  3.10E+4nMAssay Description:Inactivation of GABA-AT in rat brain homogenateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, NMDA 1 [F484A,T518L]/3A(Rattus norvegicus (Rat))
University of Copenhagen

LigandPNGBDBM213889(5,7-Dichlorokynurenic acid (5,7-DCKA))
Affinity DataKi:  3.50E+4nM ΔG°:  -25.4kJ/mole IC50:  9.70E+4nMpH: 7.4 T: 2°CAssay Description:Two-electrode voltage clamp (TEVC) recordings were performed on Xenopus oocytes at room temperature 3-6 days postinjection using an OC-725C TEVC ampl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, NMDA 1 [F484A,T518L]/3B(Rattus norvegicus (Rat))
University of Copenhagen

LigandPNGBDBM213889(5,7-Dichlorokynurenic acid (5,7-DCKA))
Affinity DataKi: >1.50E+5nM ΔG°: >-21.8kJ/mole IC50: >3.00E+5nMpH: 7.4 T: 2°CAssay Description:Two-electrode voltage clamp (TEVC) recordings were performed on Xenopus oocytes at room temperature 3-6 days postinjection using an OC-725C TEVC ampl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor 1(Rattus norvegicus (Rat))
University of Copenhagen

LigandPNGBDBM213888(1-thioxo-1,2-dihydro-[1,2,4]triazolo[4,3-a]-quinox...)
Affinity DataKi: >1.80E+5nM ΔG°: >-21.4kJ/mole IC50: >3.00E+5nMpH: 7.4 T: 2°CAssay Description:Two-electrode voltage clamp (TEVC) recordings were performed on Xenopus oocytes at room temperature 3-6 days postinjection using an OC-725C TEVC ampl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-aminobutyrate aminotransferase, mitochondrial(Homo sapiens (Human))
Northwestern University

Curated by ChEMBL
LigandPNGBDBM50118886(4-Amino-hex-5-enoic acid | CHEMBL89598 | US1018980...)
Affinity DataKi:  3.20E+6nMAssay Description:Inactivation of GABA-ATMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

Target4-aminobutyrate aminotransferase, mitochondrial(Rattus norvegicus)
Northwestern University

Curated by ChEMBL
LigandPNGBDBM50118886(4-Amino-hex-5-enoic acid | CHEMBL89598 | US1018980...)
Affinity DataKi:  1.00E+7nMAssay Description:Inactivation of GABA-AT in rat brain homogenateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, NMDA 2C(Rattus norvegicus (Rat))
University of Copenhagen

LigandPNGBDBM213888(1-thioxo-1,2-dihydro-[1,2,4]triazolo[4,3-a]-quinox...)
Affinity DataIC50:  34nMpH: 7.4 T: 2°CAssay Description:Two-electrode voltage clamp (TEVC) recordings were performed on Xenopus oocytes at room temperature 3-6 days postinjection using an OC-725C TEVC ampl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, NMDA 2B(Rattus norvegicus (Rat))
University of Copenhagen

LigandPNGBDBM213888(1-thioxo-1,2-dihydro-[1,2,4]triazolo[4,3-a]-quinox...)
Affinity DataIC50:  40nMpH: 7.4 T: 2°CAssay Description:Two-electrode voltage clamp (TEVC) recordings were performed on Xenopus oocytes at room temperature 3-6 days postinjection using an OC-725C TEVC ampl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, NMDA 2D(Rattus norvegicus (Rat))
University of Copenhagen

LigandPNGBDBM213888(1-thioxo-1,2-dihydro-[1,2,4]triazolo[4,3-a]-quinox...)
Affinity DataIC50:  160nMpH: 7.4 T: 2°CAssay Description:Two-electrode voltage clamp (TEVC) recordings were performed on Xenopus oocytes at room temperature 3-6 days postinjection using an OC-725C TEVC ampl...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 2(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50326793((+/-)(1S,2S,3R)-2-[(S)-Amino(carboxy)methyl]-3-cyc...)
Affinity DataIC50:  6.20E+4nMAssay Description:Antagonist activity at mGlu2 receptor expressed in CHO cells assessed as increase of cAMP levelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 2(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50326794((+/-)(1R,2S,3S)-3-[(S)-amino(carboxy)-methyl]-1,10...)
Affinity DataEC50: >50nMAssay Description:Agonist activity at mGlu2 receptor expressed in CHO cells assessed as inhibition of forskolin-induced increase of cAMP levelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 4(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50138781((1S,2S,3R)-2-((S)-Amino-carboxy-methyl)-3-methyl-c...)
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist activity at mGlu4 receptor expressed in CHO cells assessed as inhibition of forskolin-induced increase of cAMP levelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 4(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50326794((+/-)(1R,2S,3S)-3-[(S)-amino(carboxy)-methyl]-1,10...)
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist activity at mGlu4 receptor expressed in CHO cells assessed as inhibition of forskolin-induced increase of cAMP levelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 4(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50326793((+/-)(1S,2S,3R)-2-[(S)-Amino(carboxy)methyl]-3-cyc...)
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist activity at mGlu4 receptor expressed in CHO cells assessed as inhibition of forskolin-induced increase of cAMP levelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 2(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50331744((S)-1-(2-amino-2-carboxyethyl)-1H-1,2,3-triazole-4...)
Affinity DataEC50: >1.00E+5nMAssay Description:Binding affinity at mGluR2 expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 2(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50331745((S)-2-amino-3-(1-((S)-1-carboxy-2-phenylethyl)-1H-...)
Affinity DataEC50: >1.00E+5nMAssay Description:Binding affinity at mGluR2 expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 2(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50331746((S)-2-amino-3-(1-(carboxymethyl)-1H-1,2,3-triazol-...)
Affinity DataEC50: >1.00E+5nMAssay Description:Binding affinity at mGluR2 expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 2(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50331747((S)-2-amino-3-(1-((S)-1-carboxy-2-phenylethyl)-1H-...)
Affinity DataEC50: >1.00E+5nMAssay Description:Binding affinity at mGluR2 expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 2(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50331748((S)-2-amino-3-(1-(carboxymethyl)-1H-1,2,3-triazol-...)
Affinity DataEC50: >1.00E+5nMAssay Description:Binding affinity at mGluR2 expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 4(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50331744((S)-1-(2-amino-2-carboxyethyl)-1H-1,2,3-triazole-4...)
Affinity DataEC50: >1.00E+5nMAssay Description:Binding affinity at mGluR4 expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 4(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50331745((S)-2-amino-3-(1-((S)-1-carboxy-2-phenylethyl)-1H-...)
Affinity DataEC50: >1.00E+5nMAssay Description:Binding affinity at mGluR4 expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 4(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50331746((S)-2-amino-3-(1-(carboxymethyl)-1H-1,2,3-triazol-...)
Affinity DataEC50: >1.00E+5nMAssay Description:Binding affinity at mGluR4 expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 4(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50331747((S)-2-amino-3-(1-((S)-1-carboxy-2-phenylethyl)-1H-...)
Affinity DataEC50: >1.00E+5nMAssay Description:Binding affinity at mGluR4 expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 4(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50331748((S)-2-amino-3-(1-(carboxymethyl)-1H-1,2,3-triazol-...)
Affinity DataEC50: >1.00E+5nMAssay Description:Binding affinity at mGluR4 expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 2(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50138781((1S,2S,3R)-2-((S)-Amino-carboxy-methyl)-3-methyl-c...)
Affinity DataEC50: >10nMAssay Description:Agonist activity at mGlu2 receptor expressed in CHO cells assessed as inhibition of forskolin-induced increase of cAMP levelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 1(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50326794((+/-)(1R,2S,3S)-3-[(S)-amino(carboxy)-methyl]-1,10...)
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist activity at mGlu1 receptor expressed in CHO cells assessed as myo-[2-3H]Inositol turnover by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 1(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50326793((+/-)(1S,2S,3R)-2-[(S)-Amino(carboxy)methyl]-3-cyc...)
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist activity at mGlu1 receptor expressed in CHO cells assessed as myo-[2-3H]Inositol turnover by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMetabotropic glutamate receptor 1(Homo sapiens (Human))
The University Of Adelaide

Curated by ChEMBL
LigandPNGBDBM50138781((1S,2S,3R)-2-((S)-Amino-carboxy-methyl)-3-methyl-c...)
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist activity at mGlu1 receptor expressed in CHO cells assessed as myo-[2-3H]Inositol turnover by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed