Compile Data Set for Download or QSAR

Found 43 hits of Enzyme Inhibition Constant Data   

TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 260nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50035209(4-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 370nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049774(5-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049777(2-[1-Thiazol-5-yl-meth-(E)-ylidene]-3,4-dihydro-2H...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50009605(2-(pyridin-4-ylmethylene)-3,4-dihydronaphthalen-1(...)copy SMILEScopy InChI
Affinity DataIC50: 4.60E+3nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049765(2-[1-Pyridin-3-yl-meth-(E)-ylidene]-3,4-dihydro-2H...)copy SMILEScopy InChI
Affinity DataIC50: 9.20E+3nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049768(2-[1-Pyrazin-2-yl-meth-(E)-ylidene]-3,4-dihydro-2H...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50009605(2-(pyridin-4-ylmethylene)-3,4-dihydronaphthalen-1(...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049776(3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+4nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049766(1-Phenyl-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]naph...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049778(2-[1-(2H-Pyrazol-3-yl)-meth-(E)-ylidene]-3,4-dihyd...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+4nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049762(3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049778(2-[1-(2H-Pyrazol-3-yl)-meth-(E)-ylidene]-3,4-dihyd...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Rattus norvegicus (Rat))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049777(2-[1-Thiazol-5-yl-meth-(E)-ylidene]-3,4-dihydro-2H...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+4nMAssay Description:In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049764(2-[1-Pyridazin-3-yl-meth-(E)-ylidene]-3,4-dihydro-...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049776(3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049775(2-(Hydroxy-pyrimidin-4-yl-methyl)-3,4-dihydro-2H-n...)copy SMILEScopy InChI
Affinity DataIC50: 2.70E+4nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Rattus norvegicus (Rat))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 3.10E+4nMAssay Description:In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Rattus norvegicus (Rat))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50035209(4-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+4nMAssay Description:In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Rattus norvegicus (Rat))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50009605(2-(pyridin-4-ylmethylene)-3,4-dihydronaphthalen-1(...)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+4nMAssay Description:In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049768(2-[1-Pyrazin-2-yl-meth-(E)-ylidene]-3,4-dihydro-2H...)copy SMILEScopy InChI
Affinity DataIC50: 3.80E+4nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Rattus norvegicus (Rat))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049765(2-[1-Pyridin-3-yl-meth-(E)-ylidene]-3,4-dihydro-2H...)copy SMILEScopy InChI
Affinity DataIC50: 4.80E+4nMAssay Description:In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049762(3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 5.10E+4nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50035209(4-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 5.50E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 7.30E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Rattus norvegicus (Rat))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 7.40E+4nMAssay Description:In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Rattus norvegicus (Rat))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049776(3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 8.70E+4nMAssay Description:In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Rattus norvegicus (Rat))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049774(5-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 9.00E+4nMAssay Description:In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049774(5-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 9.00E+4nMAssay Description:Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049769(2-[1-Pyridazin-4-yl-meth-(E)-ylidene]-3,4-dihydro-...)copy SMILEScopy InChI
Affinity DataIC50: 1.03E+5nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049767(2-[1-Thiophen-3-yl-meth-(E)-ylidene]-3,4-dihydro-2...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049770(2-[1-Pyridin-2-yl-meth-(E)-ylidene]-3,4-dihydro-2H...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049772(3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049761(2-(Hydroxy-pyrazin-2-yl-methyl)-3,4-dihydro-2H-nap...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049771(2-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049780(2-(Hydroxy-pyridazin-3-yl-methyl)-3,4-dihydro-2H-n...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049782(2-[1-(2-Amino-thiazol-5-yl)-meth-(E)-ylidene]-3,4-...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049781(2-(Hydroxy-pyridazin-4-yl-methyl)-3,4-dihydro-2H-n...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049766(1-Phenyl-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]naph...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049779(2-[1-Phenyl-meth-(E)-ylidene]-3,4-dihydro-2H-napht...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
TargetAromatase(Homo sapiens (Human))
Universität de Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049764(2-[1-Pyridazin-3-yl-meth-(E)-ylidene]-3,4-dihydro-...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K499JPubMed
* indicates data uncertainty>20%