TargetAromatase(Homo sapiens (Human))
State University Of New York Upstate Medical University
Curated by ChEMBL
State University Of New York Upstate Medical University
Curated by ChEMBL
Affinity DataIC50: 9.90nMAssay Description:Inhibition of human placental aromatase using [3H]-1beta-androstenedione as substrate after 16 hrs by [3H]-water methodMore data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
State University Of New York Upstate Medical University
Curated by ChEMBL
State University Of New York Upstate Medical University
Curated by ChEMBL
Affinity DataIC50: 11.8nMAssay Description:Inhibition of human placental aromatase using [3H]-1beta-androstenedione as substrate after 16 hrs by [3H]-water methodMore data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
State University Of New York Upstate Medical University
Curated by ChEMBL
State University Of New York Upstate Medical University
Curated by ChEMBL
Affinity DataIC50: 20nMAssay Description:Inhibition of human placental aromatase using [3H]-1beta-androstenedione as substrate after 16 hrs by [3H]-water methodMore data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
State University Of New York Upstate Medical University
Curated by ChEMBL
State University Of New York Upstate Medical University
Curated by ChEMBL
Affinity DataIC50: 48.6nMAssay Description:Inhibition of human placental aromatase using [3H]-1beta-androstenedione as substrate after 16 hrs by [3H]-water methodMore data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
State University Of New York Upstate Medical University
Curated by ChEMBL
State University Of New York Upstate Medical University
Curated by ChEMBL
Affinity DataIC50: 50.1nMAssay Description:Inhibition of human placental aromatase using [3H]-1beta-androstenedione as substrate after 16 hrs by [3H]-water methodMore data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
State University Of New York Upstate Medical University
Curated by ChEMBL
State University Of New York Upstate Medical University
Curated by ChEMBL
Affinity DataIC50: 83nMAssay Description:Inhibition of human placental aromatase using [3H]-1beta-androstenedione as substrate after 16 hrs by [3H]-water methodMore data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
State University Of New York Upstate Medical University
Curated by ChEMBL
State University Of New York Upstate Medical University
Curated by ChEMBL
Affinity DataIC50: 112nMAssay Description:Inhibition of human placental aromatase using [3H]-1beta-androstenedione as substrate after 16 hrs by [3H]-water methodMore data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
State University Of New York Upstate Medical University
Curated by ChEMBL
State University Of New York Upstate Medical University
Curated by ChEMBL
Affinity DataIC50: 181nMAssay Description:Inhibition of human placental aromatase using [3H]-1beta-androstenedione as substrate after 16 hrs by [3H]-water methodMore data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
State University Of New York Upstate Medical University
Curated by ChEMBL
State University Of New York Upstate Medical University
Curated by ChEMBL
Affinity DataIC50: 2.18E+3nMAssay Description:Inhibition of human placental aromatase using [3H]-1beta-androstenedione as substrate after 16 hrs by [3H]-water methodMore data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
State University Of New York Upstate Medical University
Curated by ChEMBL
State University Of New York Upstate Medical University
Curated by ChEMBL
Affinity DataIC50: 5.20E+3nMAssay Description:Inhibition of human placental aromatase using [3H]-1beta-androstenedione as substrate after 16 hrs by [3H]-water methodMore data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
State University Of New York Upstate Medical University
Curated by ChEMBL
State University Of New York Upstate Medical University
Curated by ChEMBL
Affinity DataIC50: 1.81E+4nMAssay Description:Inhibition of human placental aromatase using [3H]-1beta-androstenedione as substrate after 16 hrs by [3H]-water methodMore data for this Ligand-Target Pair