Affinity DataIC50: 0.700nMAssay Description:In vitro inhibition of human placental Cytochrome P450 19A1More data for this Ligand-Target Pair
Affinity DataIC50: 2.90nMAssay Description:In vitro inhibition of human placental Cytochrome P450 19A1More data for this Ligand-Target Pair
Affinity DataIC50: 3.20nMAssay Description:In vitro inhibition of human placental Cytochrome P450 19A1More data for this Ligand-Target Pair
Affinity DataIC50: 3.5nMAssay Description:In vitro inhibition of human placental Cytochrome P450 19A1More data for this Ligand-Target Pair
Affinity DataIC50: 7.70nMAssay Description:In vitro inhibition of human placental Cytochrome P450 19A1More data for this Ligand-Target Pair
Affinity DataIC50: 200nMAssay Description:In vitro inhibitory concentration against human placental Cytochrome P450 19A was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 210nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 210nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1-beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 233nMAssay Description:In vitro inhibition of human placental Cytochrome P450 19A1More data for this Ligand-Target Pair
Affinity DataIC50: 300nMAssay Description:Concentration of the compound inhibiting AromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 400nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 600nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 680nMAssay Description:In vitro inhibition of human placental Cytochrome P450 19A1More data for this Ligand-Target Pair
Affinity DataIC50: 690nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.20E+3nMAssay Description:Concentration of the compound inhibiting AromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.90E+3nMAssay Description:In vitro inhibition of human placental Cytochrome P450 19A1More data for this Ligand-Target Pair
Affinity DataIC50: 2.00E+3nMAssay Description:In vitro inhibition of rat ovarian aromatase cytochrome P450 19A1More data for this Ligand-Target Pair
Affinity DataIC50: 2.20E+3nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+3nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 3.30E+3nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 4.30E+3nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 4.60E+3nMAssay Description:Concentration of the compound inhibiting AromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibition of bovine adrenal desmolaseMore data for this Ligand-Target Pair
Affinity DataIC50: 4.90E+3nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 6.20E+3nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 6.30E+3nMAssay Description:In vitro inhibitory concentration against human placental Cytochrome P450 19A was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 8.00E+3nMAssay Description:In vitro inhibition of rat ovarian aromatase cytochrome P450 19A1More data for this Ligand-Target Pair
Affinity DataIC50: 8.60E+3nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 8.90E+3nMAssay Description:In vitro inhibitory concentration against human placental Cytochrome P450 19A was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 9.30E+3nMAssay Description:In vitro inhibitory concentration against human placental Cytochrome P450 19A was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 9.60E+3nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 9.60E+3nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 9.60E+3nMAssay Description:In vitro inhibitory concentration against Aromatase was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.30E+4nMAssay Description:In vitro inhibitory concentration against human placental Cytochrome P450 19A was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.90E+4nMAssay Description:Concentration of the compound inhibiting AromataseMore data for this Ligand-Target Pair
TargetCholesterol side-chain cleavage enzyme, mitochondrial(Bos taurus (Bovine))
UniversitäT Des Saarlandes
Curated by ChEMBL
UniversitäT Des Saarlandes
Curated by ChEMBL
Affinity DataIC50: 2.90E+4nMAssay Description:Inhibition of bovine adrenal desmolaseMore data for this Ligand-Target Pair
Affinity DataIC50: 3.40E+4nMAssay Description:Inhibition of rat ovarian Cytochrome P450 19AMore data for this Ligand-Target Pair
Affinity DataIC50: 3.70E+4nMAssay Description:Inhibition of human placental aromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 3.70E+4nMAssay Description:Concentration of the compound inhibiting AromataseMore data for this Ligand-Target Pair
Affinity DataIC50: 3.70E+4nMAssay Description:In vitro inhibitory concentration against human placental Cytochrome P450 19A was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 3.70E+4nMAssay Description:In vitro inhibitory concentration against human placental Cytochrome P450 19A was determined using [1beta,2beta-3H]testosterone as radioligandMore data for this Ligand-Target Pair