Compile Data Set for Download or QSAR
Found 453 with Last Name = 'fernando' and Initial = 'dp'
TargetKetohexokinase(Homo sapiens (Human))TBA
LigandPNGBDBM319585(US10174007, Example 4 | US10787438, Example 4 | US...)copy SMILEScopy InChI
Affinity DataKi:  4.5nMAssay Description:Mixed noncompetitive inhibition of recombinant human N-terminal His-tagged KHKC expressed in Escherichia coli BL21 (DE3) using fructose as substrate ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC074MPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50133601(CHEMBL3633251)copy SMILEScopy InChI
Affinity DataKi:  151nMAssay Description:Inhibition of peroxidase activity of MPO isolated from human polynuclear leukocytes using Amplex Red as substrate assessed as formation of resorufin ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ926XPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50133602(CHEMBL3633250)copy SMILEScopy InChI
Affinity DataKi:  174nMAssay Description:Inhibition of peroxidase activity of MPO isolated from human polynuclear leukocytes using Amplex Red as substrate assessed as formation of resorufin ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ926XPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50133595(CHEMBL3633460)copy SMILEScopy InChI
Affinity DataKi:  316nMAssay Description:Inhibition of peroxidase activity of MPO isolated from human polynuclear leukocytes using Amplex Red as substrate assessed as formation of resorufin ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ926XPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50133596(CHEMBL3633459)copy SMILEScopy InChI
Affinity DataKi:  347nMAssay Description:Inhibition of peroxidase activity of MPO isolated from human polynuclear leukocytes using Amplex Red as substrate assessed as formation of resorufin ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ926XPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50133603(CHEMBL3633248)copy SMILEScopy InChI
Affinity DataKi:  372nMAssay Description:Inhibition of peroxidase activity of MPO isolated from human polynuclear leukocytes using Amplex Red as substrate assessed as formation of resorufin ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ926XPubMed
TargetMyeloperoxidase(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50133600(CHEMBL3633457)copy SMILEScopy InChI
Affinity DataKi:  501nMAssay Description:Inhibition of peroxidase activity of MPO isolated from human polynuclear leukocytes using Amplex Red as substrate assessed as formation of resorufin ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ926XPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50287520(CHEMBL4159883)copy SMILEScopy InChI
Affinity DataKi:  2.80E+4nMAssay Description:Displacement of fluorescent-labelled dofetilide from human ERG expressed in HEK293 cell membrane homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0QVZPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50287559(CHEMBL4170197)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Displacement of fluorescent-labelled dofetilide from human ERG expressed in HEK293 cell membrane homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0QVZPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50287558(CHEMBL1333494)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Displacement of fluorescent-labelled dofetilide from human ERG expressed in HEK293 cell membrane homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0QVZPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50287520(CHEMBL4159883)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Displacement of fluorescent-labelled dofetilide from human ERG expressed in HEK293 cell membrane homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0QVZPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50287552(CHEMBL4175004)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Displacement of fluorescent-labelled dofetilide from human ERG expressed in HEK293 cell membrane homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0QVZPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50287556(CHEMBL4161489)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Displacement of fluorescent-labelled dofetilide from human ERG expressed in HEK293 cell membrane homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0QVZPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50287519(CHEMBL4172084)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Displacement of fluorescent-labelled dofetilide from human ERG expressed in HEK293 cell membrane homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0QVZPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50287553(CHEMBL4166791)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Displacement of fluorescent-labelled dofetilide from human ERG expressed in HEK293 cell membrane homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0QVZPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50287554(CHEMBL4162926)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Displacement of fluorescent-labelled dofetilide from human ERG expressed in HEK293 cell membrane homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0QVZPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50287555(CHEMBL4174695)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Displacement of fluorescent-labelled dofetilide from human ERG expressed in HEK293 cell membrane homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0QVZPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50287557(CHEMBL4159568)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Displacement of fluorescent-labelled dofetilide from human ERG expressed in HEK293 cell membrane homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0QVZPubMed
TargetKetohexokinase(Homo sapiens (Human))TBA
LigandPNGBDBM319582(US10174007, Example 1 | US10787438, Example 1 | US...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of 1 nM recombinant human N-terminal His-tagged KHKC expressed in Escherichia coli BL21 (DE3) using fructose as substrate preincubated for...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC074MPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50546612(CHEMBL4753907)copy SMILES
Affinity DataIC50: 5.60nMAssay Description:Inhibition of recombinant human ACC2 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50546612(CHEMBL4753907)copy SMILES
Affinity DataIC50: 5.60nMAssay Description:Inhibition of recombinant human ACC2 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50546612(CHEMBL4753907)copy SMILES
Affinity DataIC50: 5.60nMAssay Description:Inhibition of recombinant human ACC2 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50546612(CHEMBL4753907)copy SMILES
Affinity DataIC50: 5.60nMAssay Description:Inhibition of recombinant human ACC2 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetKetohexokinase(Homo sapiens (Human))TBA
LigandPNGBDBM319582(US10174007, Example 1 | US10787438, Example 1 | US...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of 10 nM recombinant human N-terminal His-tagged KHKC expressed in Escherichia coli BL21 (DE3) using fructose as substrate preincubated fo...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC074MPubMed
TargetAcetyl-CoA carboxylase 1(Rattus norvegicus (Rat))TBA
LigandPNGBDBM50511112(CHEMBL4567446)copy SMILEScopy InChI
Affinity DataIC50: 7.5nMAssay Description:Inhibition of rat ACC1 using acetyl-CoA as substrate incubated for 20 mins in presence of [14C]O3 by liquid scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 1(Rattus norvegicus (Rat))TBA
LigandPNGBDBM50511112(CHEMBL4567446)copy SMILEScopy InChI
Affinity DataIC50: 7.5nMAssay Description:Inhibition of rat ACC1 using acetyl-CoA as substrate incubated for 20 mins in presence of [14C]O3 by liquid scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50546612(CHEMBL4753907)copy SMILES
Affinity DataIC50: 7.70nMAssay Description:Inhibition of recombinant human ACC1 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50546612(CHEMBL4753907)copy SMILES
Affinity DataIC50: 7.70nMAssay Description:Inhibition of recombinant human ACC1 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50546612(CHEMBL4753907)copy SMILES
Affinity DataIC50: 7.90nMAssay Description:Inhibition of recombinant human ACC1 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50546612(CHEMBL4753907)copy SMILES
Affinity DataIC50: 7.90nMAssay Description:Inhibition of recombinant human ACC1 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50511112(CHEMBL4567446)copy SMILEScopy InChI
Affinity DataIC50: 8.70nMAssay Description:Uncompetitive inhibition of human ACC2 incubated for 15 mins in presence of ATP by Line weaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50511112(CHEMBL4567446)copy SMILEScopy InChI
Affinity DataIC50: 8.70nMAssay Description:Uncompetitive inhibition of human ACC2 incubated for 15 mins in presence of ATP by Line weaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50546611(CHEMBL4762472)copy SMILES
Affinity DataIC50: 9.40nMAssay Description:Inhibition of recombinant human ACC2 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50546611(CHEMBL4762472)copy SMILES
Affinity DataIC50: 9.40nMAssay Description:Inhibition of recombinant human ACC2 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50546611(CHEMBL4762472)copy SMILES
Affinity DataIC50: 10nMAssay Description:Inhibition of recombinant human ACC2 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50546611(CHEMBL4762472)copy SMILES
Affinity DataIC50: 10nMAssay Description:Inhibition of recombinant human ACC2 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetKetohexokinase(Homo sapiens (Human))TBA
LigandPNGBDBM319585(US10174007, Example 4 | US10787438, Example 4 | US...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of 1 nM recombinant human N-terminal His-tagged KHKC expressed in Escherichia coli BL21 (DE3) using fructose as substrate preincubated for...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC074MPubMed
TargetAcetyl-CoA carboxylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50511112(CHEMBL4567446)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Uncompetitive inhibition of human ACC1 incubated for 15 mins in presence of ATP by Line weaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50511112(CHEMBL4567446)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Uncompetitive inhibition of human ACC1 incubated for 15 mins in presence of ATP by Line weaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50546609(CHEMBL4743101)copy SMILES
Affinity DataIC50: 13nMAssay Description:Inhibition of recombinant human ACC2 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50546609(CHEMBL4743101)copy SMILES
Affinity DataIC50: 13nMAssay Description:Inhibition of recombinant human ACC2 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50546609(CHEMBL4743101)copy SMILES
Affinity DataIC50: 13nMAssay Description:Inhibition of recombinant human ACC2 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50546609(CHEMBL4743101)copy SMILES
Affinity DataIC50: 13nMAssay Description:Inhibition of recombinant human ACC2 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetKetohexokinase(Homo sapiens (Human))TBA
LigandPNGBDBM319586(US10174007, Example 5 | US10787438, Example 5 | US...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Inhibition of 1 nM recombinant human N-terminal His-tagged KHKC expressed in Escherichia coli BL21 (DE3) using fructose as substrate preincubated for...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC074MPubMed
TargetAcetyl-CoA carboxylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50546611(CHEMBL4762472)copy SMILES
Affinity DataIC50: 16nMAssay Description:Inhibition of recombinant human ACC1 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50546611(CHEMBL4762472)copy SMILES
Affinity DataIC50: 16nMAssay Description:Inhibition of recombinant human ACC1 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50546611(CHEMBL4762472)copy SMILES
Affinity DataIC50: 17nMAssay Description:Inhibition of recombinant human ACC1 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50546611(CHEMBL4762472)copy SMILES
Affinity DataIC50: 17nMAssay Description:Inhibition of recombinant human ACC1 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50546609(CHEMBL4743101)copy SMILES
Affinity DataIC50: 20nMAssay Description:Inhibition of recombinant human ACC1 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
TargetAcetyl-CoA carboxylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50546609(CHEMBL4743101)copy SMILES
Affinity DataIC50: 20nMAssay Description:Inhibition of recombinant human ACC1 using acetyl coA as substrate incubated for 1 hr by transcreener fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR22VTPubMed
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