Compile Data Set for Download or QSAR
Found 13 with Last Name = 'wang' and Initial = 'km'
TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM50405578(CHEMBL5273222)copy SMILEScopy InChI
Affinity DataIC50: 9.90E+3nMAssay Description:The compound was evaluated for the antagonistic activity against beta-1 adrenergic receptorMore data for this Ligand-Target Pair
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TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM50405574(CHEMBL5286422)copy SMILEScopy InChI
Affinity DataIC50: 3.02E+4nMAssay Description:In vitro concentration required to inhibit partially purified dihydropteroate synthase of Escherichia coli by 50%More data for this Ligand-Target Pair
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TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM50405581(CHEMBL5269761)copy SMILEScopy InChI
Affinity DataIC50: 3.54E+4nMAssay Description:In vitro inhibitory activity against beta-2 adrenergic receptor was measured by the inhibition of isoproterenol-induced relaxation of PGF2-alpha cont...More data for this Ligand-Target Pair
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TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM50405575(CHEMBL5270418)copy SMILEScopy InChI
Affinity DataIC50: 4.53E+4nMAssay Description:In vitro concentration required to inhibit partially purified dihydropteroate synthase of Escherichia coli by 50%More data for this Ligand-Target Pair
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TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM50405580(CHEMBL5268974)copy SMILEScopy InChI
Affinity DataIC50: 6.34E+4nMAssay Description:In vitro inhibitory activity against beta-2 adrenergic receptor was measured by the inhibition of isoproterenol-induced relaxation of PGF2-alpha cont...More data for this Ligand-Target Pair
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TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM50405576(CHEMBL5285158)copy SMILEScopy InChI
Affinity DataIC50: 6.41E+4nMAssay Description:The compound was evaluated for the antagonistic activity against beta-2 adrenergic receptor.More data for this Ligand-Target Pair
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TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM50405572(CHEMBL5267745)copy SMILEScopy InChI
Affinity DataIC50: 8.25E+4nMAssay Description:In vitro concentration required to inhibit partially purified dihydropteroate synthase of Escherichia coli by 50%More data for this Ligand-Target Pair
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TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM50405571(CHEMBL5281437)copy SMILEScopy InChI
Affinity DataIC50: 8.76E+4nMAssay Description:In vitro concentration required to inhibit partially purified dihydropteroate synthase of Escherichia coli by 50%More data for this Ligand-Target Pair
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TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM50405579(CHEMBL5283357)copy SMILEScopy InChI
Affinity DataIC50: 8.78E+4nMAssay Description:The compound was evaluated for the antagonistic activity against beta-2 adrenergic receptor.More data for this Ligand-Target Pair
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TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM50405573(CHEMBL5283691)copy SMILEScopy InChI
Affinity DataIC50: 9.36E+4nMAssay Description:In vitro concentration required to inhibit partially purified dihydropteroate synthase of Escherichia coli by 50%More data for this Ligand-Target Pair
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TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM50242271((2R,3R,4R,5S)-1-(2-hydroxyethyl)-2-(hydroxymethyl)...)copy SMILEScopy InChI
Affinity DataIC50: 1.54E+5nMAssay Description:In vitro inhibitory activity against beta-2 adrenergic receptor was measured by the inhibition of isoproterenol-induced relaxation of PGF2-alpha cont...More data for this Ligand-Target Pair
TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM23406((3R,4R,5S,6R)-5-{[(2R,3R,4R,5S,6R)-5-{[(2R,3R,4S,5...)copy SMILEScopy InChI
Affinity DataIC50: 2.59E+5nMAssay Description:In vitro inhibitory activity against beta-2 adrenergic receptor was measured by the inhibition of isoproterenol-induced relaxation of PGF2-alpha cont...More data for this Ligand-Target Pair
TargetMaltase-glucoamylase(Homo sapiens (Human))TBA
LigandPNGBDBM50405577(CHEMBL5271561)copy SMILEScopy InChI
Affinity DataIC50: 5.07E+5nMAssay Description:The compound was evaluated for the antagonistic activity against beta-2 adrenergic receptor.More data for this Ligand-Target Pair
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