Compile Data Set for Download or QSAR
maximum 50k data
Found 43 Enz. Inhib. hit(s) with all data for entry = 50006491
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049763(2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50035209(4-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049774(5-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049777(2-[1-Thiazol-5-yl-meth-(E)-ylidene]-3,4-dihydro-2H...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50009605(2-(pyridin-4-ylmethylene)-3,4-dihydronaphthalen-1(...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049765(2-[1-Pyridin-3-yl-meth-(E)-ylidene]-3,4-dihydro-2H...)
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 ArticlePubMed
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...)
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 ArticlePubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50009605(2-(pyridin-4-ylmethylene)-3,4-dihydronaphthalen-1(...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049776(3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)
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 ArticlePubMed
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...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049778(2-[1-(2H-Pyrazol-3-yl)-meth-(E)-ylidene]-3,4-dihyd...)
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 ArticlePubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049762(3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)
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 ArticlePubMed
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...)
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 ArticlePubMed
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-...)
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 ArticlePubMed
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...)
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 ArticlePubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049776(3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049775(2-(Hydroxy-pyrimidin-4-yl-methyl)-3,4-dihydro-2H-n...)
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 ArticlePubMed
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...)
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 ArticlePubMed
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...)
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 ArticlePubMed
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(...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049768(2-[1-Pyrazin-2-yl-meth-(E)-ylidene]-3,4-dihydro-2H...)
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 ArticlePubMed
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...)
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 ArticlePubMed
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...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049762(3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)
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 ArticlePubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50035209(4-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)
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 ArticlePubMed
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...)
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 ArticlePubMed
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...)
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 ArticlePubMed
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...)
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 ArticlePubMed
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...)
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 ArticlePubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049774(5-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049769(2-[1-Pyridazin-4-yl-meth-(E)-ylidene]-3,4-dihydro-...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049782(2-[1-(2-Amino-thiazol-5-yl)-meth-(E)-ylidene]-3,4-...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049781(2-(Hydroxy-pyridazin-4-yl-methyl)-3,4-dihydro-2H-n...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049780(2-(Hydroxy-pyridazin-3-yl-methyl)-3,4-dihydro-2H-n...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049779(2-[1-Phenyl-meth-(E)-ylidene]-3,4-dihydro-2H-napht...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049761(2-(Hydroxy-pyrazin-2-yl-methyl)-3,4-dihydro-2H-nap...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049767(2-[1-Thiophen-3-yl-meth-(E)-ylidene]-3,4-dihydro-2...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049764(2-[1-Pyridazin-3-yl-meth-(E)-ylidene]-3,4-dihydro-...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049771(2-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049766(1-Phenyl-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]naph...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049770(2-[1-Pyridin-2-yl-meth-(E)-ylidene]-3,4-dihydro-2H...)
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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
UniversitäT De Saarlandes

Curated by ChEMBL
LigandPNGBDBM50049772(3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...)
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 ArticlePubMed