Compile Data Set for Download or QSAR

Found 71 hits with Last Name = 'sergejew' and Initial = 't'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Aromatase (Homo sapiens (Human))	BDBM50035208 (1-Pyridin-4-yl-1a,2,3,7b-tetrahydro-1H-cyclopropa[...) Show SMILES Oc1ccc2CCC3C(C3c2c1)c1ccncc1 Show InChI InChI=1S/C16H15NO/c18-12-3-1-10-2-4-13-15(16(13)14(10)9-12)11-5-7-17-8-6-11/h1,3,5-9,13,15-16,18H,2,4H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	66	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50035206 (4-(5-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...) Show SMILES COc1ccc2C3C(CCc2c1)C3c1ccncc1 Show InChI InChI=1S/C17H17NO/c1-19-13-3-5-14-12(10-13)2-4-15-16(17(14)15)11-6-8-18-9-7-11/h3,5-10,15-17H,2,4H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	69	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50049763 (2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...) Show SMILES O=C1C(CCc2ccccc12)=Cc1cnc[nH]1 |w:11.13| Show InChI InChI=1S/C14H12N2O/c17-14-11(7-12-8-15-9-16-12)6-5-10-3-1-2-4-13(10)14/h1-4,7-9H,5-6H2,(H,15,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	170	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50035209 (4-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...) Show SMILES C1Cc2ccccc2C2C1C2c1ccncc1 Show InChI InChI=1S/C16H15N/c1-2-4-13-11(3-1)5-6-14-15(16(13)14)12-7-9-17-10-8-12/h1-4,7-10,14-16H,5-6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	185	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50049763 (2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...) Show SMILES O=C1C(CCc2ccccc12)=Cc1cnc[nH]1 |w:11.13| Show InChI InChI=1S/C14H12N2O/c17-14-11(7-12-8-15-9-16-12)6-5-10-3-1-2-4-13(10)14/h1-4,7-9H,5-6H2,(H,15,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50035204 (4-(6-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...) Show SMILES COc1ccc2CCC3C(C3c2c1)c1ccncc1 Show InChI InChI=1S/C17H17NO/c1-19-13-4-2-11-3-5-14-16(17(14)15(11)10-13)12-6-8-18-9-7-12/h2,4,6-10,14,16-17H,3,5H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	265	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description In vitro inhibition of rat ovarian microsomal Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50035211 (1-Pyridin-4-yl-1a,2,3,7b-tetrahydro-1H-cyclopropa[...) Show SMILES Oc1ccc2C3C(CCc2c1)C3c1ccncc1 Show InChI InChI=1S/C16H15NO/c18-12-2-4-13-11(9-12)1-3-14-15(16(13)14)10-5-7-17-8-6-10/h2,4-9,14-16,18H,1,3H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	330	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50035209 (4-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...) Show SMILES C1Cc2ccccc2C2C1C2c1ccncc1 Show InChI InChI=1S/C16H15N/c1-2-4-13-11(3-1)5-6-14-15(16(13)14)12-7-9-17-10-8-12/h1-4,7-10,14-16H,5-6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	370	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50035213 (4-(6-Methoxy-1-methyl-1a,2,3,7b-tetrahydro-1H-cycl...) Show SMILES COc1ccc2CCC3C(c2c1)C3(C)c1ccncc1 Show InChI InChI=1S/C18H19NO/c1-18(13-7-9-19-10-8-13)16-6-4-12-3-5-14(20-2)11-15(12)17(16)18/h3,5,7-11,16-17H,4,6H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	370	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Rattus norvegicus)	BDBM8611 (4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...) Show SMILES N#Cc1ccc(cc1)C1CCCc2cncn12 Show InChI InChI=1S/C14H13N3/c15-8-11-4-6-12(7-5-11)14-3-1-2-13-9-16-10-17(13)14/h4-7,9-10,14H,1-3H2	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description In vitro inhibition of ACTH-stimulated aldosterone biosynthesis in rat adrenal slices				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50049774 (5-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...) Show SMILES C1Cc2ccccc2C2C1C2c1cnc[nH]1 Show InChI InChI=1S/C14H14N2/c1-2-4-10-9(3-1)5-6-11-13(10)14(11)12-7-15-8-16-12/h1-4,7-8,11,13-14H,5-6H2,(H,15,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50035205 (4-(5-Bromo-6-methoxy-1a,2,3,7b-tetrahydro-1H-cyclo...) Show SMILES COc1cc2C3C(CCc2cc1Br)C3c1ccncc1 Show InChI InChI=1S/C17H16BrNO/c1-20-15-9-13-11(8-14(15)18)2-3-12-16(17(12)13)10-4-6-19-7-5-10/h4-9,12,16-17H,2-3H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	920	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50035205 (4-(5-Bromo-6-methoxy-1a,2,3,7b-tetrahydro-1H-cyclo...) Show SMILES COc1cc2C3C(CCc2cc1Br)C3c1ccncc1 Show InChI InChI=1S/C17H16BrNO/c1-20-15-9-13-11(8-14(15)18)2-3-12-16(17(12)13)10-4-6-19-7-5-10/h4-9,12,16-17H,2-3H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	920	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50049777 (2-[1-Thiazol-5-yl-meth-(E)-ylidene]-3,4-dihydro-2H...) Show SMILES O=C1\C(CCc2ccccc12)=C\c1cncs1 Show InChI InChI=1S/C14H11NOS/c16-14-11(7-12-8-15-9-17-12)6-5-10-3-1-2-4-13(10)14/h1-4,7-9H,5-6H2/b11-7+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Rattus norvegicus)	BDBM50035209 (4-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...) Show SMILES C1Cc2ccccc2C2C1C2c1ccncc1 Show InChI InChI=1S/C16H15N/c1-2-4-13-11(3-1)5-6-14-15(16(13)14)12-7-9-17-10-8-12/h1-4,7-10,14-16H,5-6H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description In vitro inhibition of ACTH-stimulated aldosterone biosynthesis in rat adrenal slices				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50035212 (4-(4-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...) Show SMILES COc1cccc2C3C(CCc12)C3c1ccncc1 Show InChI InChI=1S/C17H17NO/c1-19-15-4-2-3-13-12(15)5-6-14-16(17(13)14)11-7-9-18-10-8-11/h2-4,7-10,14,16-17H,5-6H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.35E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50035210 (4-(7-Bromo-4-methoxy-1a,2,3,7b-tetrahydro-1H-cyclo...) Show SMILES COc1ccc(Br)c2C3C(CCc12)C3c1ccncc1 Show InChI InChI=1S/C17H16BrNO/c1-20-14-5-4-13(18)16-11(14)2-3-12-15(17(12)16)10-6-8-19-9-7-10/h4-9,12,15,17H,2-3H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	4.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50009605 (2-(pyridin-4-ylmethylene)-3,4-dihydronaphthalen-1(...) Show SMILES O=C1\C(CCc2ccccc12)=C\c1ccncc1 Show InChI InChI=1S/C16H13NO/c18-16-14(11-12-7-9-17-10-8-12)6-5-13-3-1-2-4-15(13)16/h1-4,7-11H,5-6H2/b14-11+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50035207 (1-(pyridin-4-yl)-1a,2,3,7b-tetrahydro-1H-cycloprop...) Show SMILES Oc1cccc2C3C(CCc12)C3c1ccncc1 Show InChI InChI=1S/C16H15NO/c18-14-3-1-2-12-11(14)4-5-13-15(16(12)13)10-6-8-17-9-7-10/h1-3,6-9,13,15-16,18H,4-5H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM9460 (3-(4-aminophenyl)-3-ethyl-piperidine-2,6-dione | 3...) Show SMILES CCC1(CCC(=O)NC1=O)c1ccc(N)cc1 Show InChI InChI=1S/C13H16N2O2/c1-2-13(8-7-11(16)15-12(13)17)9-3-5-10(14)6-4-9/h3-6H,2,7-8,14H2,1H3,(H,15,16,17)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank KEGG PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	6.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description In vitro inhibition of rat ovarian microsomal Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Rattus norvegicus)	BDBM50035208 (1-Pyridin-4-yl-1a,2,3,7b-tetrahydro-1H-cyclopropa[...) Show SMILES Oc1ccc2CCC3C(C3c2c1)c1ccncc1 Show InChI InChI=1S/C16H15NO/c18-12-3-1-10-2-4-13-15(16(13)14(10)9-12)11-5-7-17-8-6-11/h1,3,5-9,13,15-16,18H,2,4H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description In vitro inhibition of ACTH-stimulated aldosterone biosynthesis in rat adrenal slices				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50049765 (2-[1-Pyridin-3-yl-meth-(E)-ylidene]-3,4-dihydro-2H...) Show SMILES O=C1\C(CCc2ccccc12)=C\c1cccnc1 Show InChI InChI=1S/C16H13NO/c18-16-14(10-12-4-3-9-17-11-12)8-7-13-5-1-2-6-15(13)16/h1-6,9-11H,7-8H2/b14-10+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Rattus norvegicus)	BDBM50035204 (4-(6-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...) Show SMILES COc1ccc2CCC3C(C3c2c1)c1ccncc1 Show InChI InChI=1S/C17H17NO/c1-19-13-4-2-11-3-5-14-16(17(14)15(11)10-13)12-6-8-18-9-7-12/h2,4,6-10,14,16-17H,3,5H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description In vitro inhibition of ACTH-stimulated aldosterone biosynthesis in rat adrenal slices				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50035204 (4-(6-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...) Show SMILES COc1ccc2CCC3C(C3c2c1)c1ccncc1 Show InChI InChI=1S/C17H17NO/c1-19-13-4-2-11-3-5-14-16(17(14)15(11)10-13)12-6-8-18-9-7-12/h2,4,6-10,14,16-17H,3,5H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50035204 (4-(6-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...) Show SMILES COc1ccc2CCC3C(C3c2c1)c1ccncc1 Show InChI InChI=1S/C17H17NO/c1-19-13-4-2-11-3-5-14-16(17(14)15(11)10-13)12-6-8-18-9-7-12/h2,4,6-10,14,16-17H,3,5H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM50049768 (2-[1-Pyrazin-2-yl-meth-(E)-ylidene]-3,4-dihydro-2H...) Show SMILES O=C1\C(CCc2ccccc12)=C\c1cnccn1 Show InChI InChI=1S/C15H12N2O/c18-15-12(9-13-10-16-7-8-17-13)6-5-11-3-1-2-4-14(11)15/h1-4,7-10H,5-6H2/b12-9+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Rattus norvegicus)	BDBM50035204 (4-(6-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...) Show SMILES COc1ccc2CCC3C(C3c2c1)c1ccncc1 Show InChI InChI=1S/C17H17NO/c1-19-13-4-2-11-3-5-14-16(17(14)15(11)10-13)12-6-8-18-9-7-12/h2,4,6-10,14,16-17H,3,5H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description In vitro inhibition of ACTH-stimulated aldosterone biosynthesis in rat adrenal slices				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Rattus norvegicus)	BDBM50378780 ((S)-VOROZOLE) Show SMILES Cn1nnc2ccc(cc12)[C@H](c1ccc(Cl)cc1)n1cncn1 |r| Show InChI InChI=1S/C16H13ClN6/c1-22-15-8-12(4-7-14(15)20-21-22)16(23-10-18-9-19-23)11-2-5-13(17)6-3-11/h2-10,16H,1H3/t16-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description In vitro inhibition of ACTH-stimulated aldosterone biosynthesis in rat adrenal slices				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM50009605 (2-(pyridin-4-ylmethylene)-3,4-dihydronaphthalen-1(...) Show SMILES O=C1\C(CCc2ccccc12)=C\c1ccncc1 Show InChI InChI=1S/C16H13NO/c18-16-14(11-12-7-9-17-10-8-12)6-5-13-3-1-2-4-15(13)16/h1-4,7-11H,5-6H2/b14-11+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50049776 (3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...) Show SMILES C1Cc2ccccc2C2C1C2c1cccnc1 Show InChI InChI=1S/C16H15N/c1-2-6-13-11(4-1)7-8-14-15(16(13)14)12-5-3-9-17-10-12/h1-6,9-10,14-16H,7-8H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM50049766 (1-Phenyl-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]naph...) Show SMILES C1Cc2ccccc2C2C1C2c1ccccc1 Show InChI InChI=1S/C17H16/c1-2-7-13(8-3-1)16-15-11-10-12-6-4-5-9-14(12)17(15)16/h1-9,15-17H,10-11H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50049778 (2-[1-(2H-Pyrazol-3-yl)-meth-(E)-ylidene]-3,4-dihyd...) Show SMILES O=C1C(CCc2ccccc12)=Cc1ccn[nH]1 |w:11.13| Show InChI InChI=1S/C14H12N2O/c17-14-11(9-12-7-8-15-16-12)6-5-10-3-1-2-4-13(10)14/h1-4,7-9H,5-6H2,(H,15,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM9460 (3-(4-aminophenyl)-3-ethyl-piperidine-2,6-dione | 3...) Show SMILES CCC1(CCC(=O)NC1=O)c1ccc(N)cc1 Show InChI InChI=1S/C13H16N2O2/c1-2-13(8-7-11(16)15-12(13)17)9-3-5-10(14)6-4-9/h3-6H,2,7-8,14H2,1H3,(H,15,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank KEGG PC cid PC sid PDB UniChem Patents Similars	DrugBank PubMed	n/a	n/a	1.85E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of Human placental Cytochrome P450 19A1				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM50049762 (3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...) Show SMILES C1Cc2ccccc2C2C1C2c1ccn[nH]1 Show InChI InChI=1S/C14H14N2/c1-2-4-10-9(3-1)5-6-11-13(10)14(11)12-7-8-15-16-12/h1-4,7-8,11,13-14H,5-6H2,(H,15,16)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM50049778 (2-[1-(2H-Pyrazol-3-yl)-meth-(E)-ylidene]-3,4-dihyd...) Show SMILES O=C1C(CCc2ccccc12)=Cc1ccn[nH]1 |w:11.13| Show InChI InChI=1S/C14H12N2O/c17-14-11(9-12-7-8-15-16-12)6-5-10-3-1-2-4-13(10)14/h1-4,7-9H,5-6H2,(H,15,16)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Steroid 17-alpha-hydroxylase/17,20 lyase (Rattus norvegicus (Rat))	BDBM50049777 (2-[1-Thiazol-5-yl-meth-(E)-ylidene]-3,4-dihydro-2H...) Show SMILES O=C1\C(CCc2ccccc12)=C\c1cncs1 Show InChI InChI=1S/C14H11NOS/c16-14-11(7-12-8-15-9-17-12)6-5-10-3-1-2-4-13(10)14/h1-4,7-9H,5-6H2/b11-7+	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM50049764 (2-[1-Pyridazin-3-yl-meth-(E)-ylidene]-3,4-dihydro-...) Show SMILES O=C1\C(CCc2ccccc12)=C\c1cccnn1 Show InChI InChI=1S/C15H12N2O/c18-15-12(10-13-5-3-9-16-17-13)8-7-11-4-1-2-6-14(11)15/h1-6,9-10H,7-8H2/b12-10+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM50049776 (3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...) Show SMILES C1Cc2ccccc2C2C1C2c1cccnc1 Show InChI InChI=1S/C16H15N/c1-2-6-13-11(4-1)7-8-14-15(16(13)14)12-5-3-9-17-10-12/h1-6,9-10,14-16H,7-8H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50049775 (2-(Hydroxy-pyrimidin-4-yl-methyl)-3,4-dihydro-2H-n...) Show SMILES OC(C1CCc2ccccc2C1=O)c1ccncn1 Show InChI InChI=1S/C15H14N2O2/c18-14-11-4-2-1-3-10(11)5-6-12(14)15(19)13-7-8-16-9-17-13/h1-4,7-9,12,15,19H,5-6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Cytochrome P450 11B1, mitochondrial (Homo sapiens (Human))	BDBM50035204 (4-(6-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...) Show SMILES COc1ccc2CCC3C(C3c2c1)c1ccncc1 Show InChI InChI=1S/C17H17NO/c1-19-13-4-2-11-3-5-14-16(17(14)15(11)10-13)12-6-8-18-9-7-12/h2,4,6-10,14,16-17H,3,5H2,1H3	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description In vitro inhibition of ACTH-stimulated corticosterone biosynthesis in rat adrenal slices				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Cytochrome P450 11B1, mitochondrial (Homo sapiens (Human))	BDBM50035204 (4-(6-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...) Show SMILES COc1ccc2CCC3C(C3c2c1)c1ccncc1 Show InChI InChI=1S/C17H17NO/c1-19-13-4-2-11-3-5-14-16(17(14)15(11)10-13)12-6-8-18-9-7-12/h2,4,6-10,14,16-17H,3,5H2,1H3	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description In vitro inhibition of ACTH-stimulated corticosterone biosynthesis in rat adrenal slices				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Steroid 17-alpha-hydroxylase/17,20 lyase (Rattus norvegicus (Rat))	BDBM50049763 (2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...) Show SMILES O=C1C(CCc2ccccc12)=Cc1cnc[nH]1 |w:11.13| Show InChI InChI=1S/C14H12N2O/c17-14-11(7-12-8-15-9-16-12)6-5-10-3-1-2-4-13(10)14/h1-4,7-9H,5-6H2,(H,15,16)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Steroid 17-alpha-hydroxylase/17,20 lyase (Rattus norvegicus (Rat))	BDBM50035209 (4-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...) Show SMILES C1Cc2ccccc2C2C1C2c1ccncc1 Show InChI InChI=1S/C16H15N/c1-2-4-13-11(3-1)5-6-14-15(16(13)14)12-7-9-17-10-8-12/h1-4,7-10,14-16H,5-6H2	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Steroid 17-alpha-hydroxylase/17,20 lyase (Rattus norvegicus (Rat))	BDBM50009605 (2-(pyridin-4-ylmethylene)-3,4-dihydronaphthalen-1(...) Show SMILES O=C1\C(CCc2ccccc12)=C\c1ccncc1 Show InChI InChI=1S/C16H13NO/c18-16-14(11-12-7-9-17-10-8-12)6-5-13-3-1-2-4-15(13)16/h1-4,7-11H,5-6H2/b14-11+	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50049768 (2-[1-Pyrazin-2-yl-meth-(E)-ylidene]-3,4-dihydro-2H...) Show SMILES O=C1\C(CCc2ccccc12)=C\c1cnccn1 Show InChI InChI=1S/C15H12N2O/c18-15-12(9-13-10-16-7-8-17-13)6-5-11-3-1-2-4-14(11)15/h1-4,7-10H,5-6H2/b12-9+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM50049763 (2-[1-(3H-Imidazol-4-yl)-meth-(E)-ylidene]-3,4-dihy...) Show SMILES O=C1C(CCc2ccccc12)=Cc1cnc[nH]1 |w:11.13| Show InChI InChI=1S/C14H12N2O/c17-14-11(7-12-8-15-9-16-12)6-5-10-3-1-2-4-13(10)14/h1-4,7-9H,5-6H2,(H,15,16)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Steroid 17-alpha-hydroxylase/17,20 lyase (Rattus norvegicus (Rat))	BDBM50049765 (2-[1-Pyridin-3-yl-meth-(E)-ylidene]-3,4-dihydro-2H...) Show SMILES O=C1\C(CCc2ccccc12)=C\c1cccnc1 Show InChI InChI=1S/C16H13NO/c18-16-14(10-12-4-3-9-17-11-12)8-7-13-5-1-2-6-15(13)16/h1-6,9-11H,7-8H2/b14-10+	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Steroidgenic Cytochrome P450 17 alpha using rat testicular microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Rattus norvegicus)	BDBM9460 (3-(4-aminophenyl)-3-ethyl-piperidine-2,6-dione | 3...) Show SMILES CCC1(CCC(=O)NC1=O)c1ccc(N)cc1 Show InChI InChI=1S/C13H16N2O2/c1-2-13(8-7-11(16)15-12(13)17)9-3-5-10(14)6-4-9/h3-6H,2,7-8,14H2,1H3,(H,15,16,17)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank KEGG PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description In vitro inhibition of ACTH-stimulated aldosterone biosynthesis in rat adrenal slices				J Med Chem 38: 2103-11 (1995) BindingDB Entry DOI: 10.7270/Q2NV9H9S
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50049762 (3-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...) Show SMILES C1Cc2ccccc2C2C1C2c1ccn[nH]1 Show InChI InChI=1S/C14H14N2/c1-2-4-10-9(3-1)5-6-11-13(10)14(11)12-7-8-15-16-12/h1-4,7-8,11,13-14H,5-6H2,(H,15,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description In vitro inhibitory activity against Cytochrome P450 19A1 using human placental microsomes.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM50035209 (4-(1a,2,3,7b-Tetrahydro-1H-cyclopropa[a]naphthalen...) Show SMILES C1Cc2ccccc2C2C1C2c1ccncc1 Show InChI InChI=1S/C16H15N/c1-2-4-13-11(3-1)5-6-14-15(16(13)14)12-7-9-17-10-8-12/h1-4,7-10,14-16H,5-6H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität de Saarlandes Curated by ChEMBL					Assay Description Inhibitory activity against Steroidgenic Cytochrome P450 C18 using Bovine adrenal mitochondria.				J Med Chem 39: 834-41 (1996) Article DOI: 10.1021/jm950377t BindingDB Entry DOI: 10.7270/Q29K499J
					More data for this Ligand-Target Pair

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