Compile Data Set for Download or QSAR

Found 42 hits Enz. Inhib. hit(s) with all data for entry = 50033106   

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
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	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	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human CYP11B2 expressed in Chinese hamster V79MZ cells using [1,2-3H]11-deoxycorticosterone/11-deoxycorticosterone				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair				3D Structure (crystal)
Cytochrome P450 11B1, mitochondrial (Homo sapiens (Human))	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	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human CYP11B1 expressed in Chinese hamster V79MZ cells using [1,2-3H]11-deoxycorticosterone/11-deoxycorticosterone				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair				3D Structure (crystal)
Aromatase (Homo sapiens (Human))	BDBM50339655 (7-(3,4-Difluorophenoxy)-4-(1H-imidazol-1-ylmethyl)...) Show SMILES Fc1ccc(Oc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)cc1F Show InChI InChI=1S/C19H12F2N2O3/c20-16-4-2-13(8-17(16)21)25-14-1-3-15-12(10-23-6-5-22-11-23)7-19(24)26-18(15)9-14/h1-9,11H,10H2	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	47	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM9475 (4-(1H-Imidazol-1-ylmethyl)-7-phenoxy-2H-chromen-2-...) Show SMILES O=c1cc(Cn2ccnc2)c2ccc(Oc3ccccc3)cc2o1 Show InChI InChI=1S/C19H14N2O3/c22-19-10-14(12-21-9-8-20-13-21)17-7-6-16(11-18(17)24-19)23-15-4-2-1-3-5-15/h1-11,13H,12H2	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	51	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	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	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	52	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339659 (CHEMBL1688915 | rac-4-[1H-Imidazol-1-yl(phenyl)met...) Show SMILES O=c1cc(C(c2ccccc2)n2ccnc2)c2ccc(Oc3ccccc3)cc2o1 Show InChI InChI=1S/C25H18N2O3/c28-24-16-22(25(27-14-13-26-17-27)18-7-3-1-4-8-18)21-12-11-20(15-23(21)30-24)29-19-9-5-2-6-10-19/h1-17,25H	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	67	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339654 (7-(3,5-Difluorophenoxy)-4-(1H-imidazol-1-ylmethyl)...) Show SMILES Fc1cc(F)cc(Oc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)c1 Show InChI InChI=1S/C19H12F2N2O3/c20-13-6-14(21)8-16(7-13)25-15-1-2-17-12(10-23-4-3-22-11-23)5-19(24)26-18(17)9-15/h1-9,11H,10H2	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	70	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339646 (7-(3-Fluorophenoxy)-4-(1H-imidazol-1-ylmethyl)-2H-...) Show SMILES Fc1cccc(Oc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)c1 Show InChI InChI=1S/C19H13FN2O3/c20-14-2-1-3-15(9-14)24-16-4-5-17-13(11-22-7-6-21-12-22)8-19(23)25-18(17)10-16/h1-10,12H,11H2	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	72	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Cytochrome P450 11B1, mitochondrial (Homo sapiens (Human))	BDBM9485 (7-(benzyloxy)-4-(1H-imidazol-1-ylmethyl)-2H-chrome...) Show SMILES O=c1cc(Cn2ccnc2)c2ccc(OCc3ccccc3)cc2o1 Show InChI InChI=1S/C20H16N2O3/c23-20-10-16(12-22-9-8-21-14-22)18-7-6-17(11-19(18)25-20)24-13-15-4-2-1-3-5-15/h1-11,14H,12-13H2	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	72	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human CYP11B1 expressed in Chinese hamster V79MZ cells using [1,2-3H]11-deoxycorticosterone/11-deoxycorticosterone				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339647 (7-(3-Chlorophenoxy)-4-(1H-imidazol-1-ylmethyl)-2H-...) Show SMILES Clc1cccc(Oc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)c1 Show InChI InChI=1S/C19H13ClN2O3/c20-14-2-1-3-15(9-14)24-16-4-5-17-13(11-22-7-6-21-12-22)8-19(23)25-18(17)10-16/h1-10,12H,11H2	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	72	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339653 (7-[4-(Dimethylamino)phenoxy]-4-(1H-imidazol-1-ylme...) Show SMILES CN(C)c1ccc(Oc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)cc1 Show InChI InChI=1S/C21H19N3O3/c1-23(2)16-3-5-17(6-4-16)26-18-7-8-19-15(13-24-10-9-22-14-24)11-21(25)27-20(19)12-18/h3-12,14H,13H2,1-2H3	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	81	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339656 (7-Anilino-4-(1H-imidazol-1-ylmethyl)-2H-chromen-2-...) Show SMILES O=c1cc(Cn2ccnc2)c2ccc(Nc3ccccc3)cc2o1 Show InChI InChI=1S/C19H15N3O2/c23-19-10-14(12-22-9-8-20-13-22)17-7-6-16(11-18(17)24-19)21-15-4-2-1-3-5-15/h1-11,13,21H,12H2	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	105	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339650 (7-(4-Chlorophenoxy)-4-(1H-imidazol-1-ylmethyl)-2H-...) Show SMILES Clc1ccc(Oc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)cc1 Show InChI InChI=1S/C19H13ClN2O3/c20-14-1-3-15(4-2-14)24-16-5-6-17-13(11-22-8-7-21-12-22)9-19(23)25-18(17)10-16/h1-10,12H,11H2	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	112	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339665 (7-[(3-Fluorobenzyl)oxy]-4-(1H-imidazol-1-ylmethyl)...) Show SMILES Fc1cccc(COc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)c1 Show InChI InChI=1S/C20H15FN2O3/c21-16-3-1-2-14(8-16)12-25-17-4-5-18-15(11-23-7-6-22-13-23)9-20(24)26-19(18)10-17/h1-10,13H,11-12H2	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	113	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339664 (4-(1H-Imidazol-1-ylmethyl)-7-[(3-methylbenzyl)oxy]...) Show SMILES Cc1cccc(COc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)c1 Show InChI InChI=1S/C21H18N2O3/c1-15-3-2-4-16(9-15)13-25-18-5-6-19-17(12-23-8-7-22-14-23)10-21(24)26-20(19)11-18/h2-11,14H,12-13H2,1H3	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	114	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339642 (4-(1H-Imidazol-1-ylmethyl)-7-[(4-methoxybenzyl)oxy...) Show SMILES COc1ccc(COc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)cc1 Show InChI InChI=1S/C21H18N2O4/c1-25-17-4-2-15(3-5-17)13-26-18-6-7-19-16(12-23-9-8-22-14-23)10-21(24)27-20(19)11-18/h2-11,14H,12-13H2,1H3	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	127	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339666 (7-[(3-Chlorobenzyl)oxy]-4-(1H-imidazol-1-ylmethyl)...) Show SMILES Clc1cccc(COc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)c1 Show InChI InChI=1S/C20H15ClN2O3/c21-16-3-1-2-14(8-16)12-25-17-4-5-18-15(11-23-7-6-22-13-23)9-20(24)26-19(18)10-17/h1-10,13H,11-12H2	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	130	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339669 (4-(1H-Imidazol-1-ylmethyl)-7-[(3-nitrobenzyl)oxy]-...) Show SMILES [O-][N+](=O)c1cccc(COc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)c1 Show InChI InChI=1S/C20H15N3O5/c24-20-9-15(11-22-7-6-21-13-22)18-5-4-17(10-19(18)28-20)27-12-14-2-1-3-16(8-14)23(25)26/h1-10,13H,11-12H2	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	141	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM9485 (7-(benzyloxy)-4-(1H-imidazol-1-ylmethyl)-2H-chrome...) Show SMILES O=c1cc(Cn2ccnc2)c2ccc(OCc3ccccc3)cc2o1 Show InChI InChI=1S/C20H16N2O3/c23-20-10-16(12-22-9-8-21-14-22)18-7-6-17(11-19(18)25-20)24-13-15-4-2-1-3-5-15/h1-11,14H,12-13H2	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	150	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339651 (4-{[4-(1H-Imidazol-1-ylmethyl)-2-oxo-2H-chromen-7-...) Show SMILES O=c1cc(Cn2ccnc2)c2ccc(Oc3ccc(cc3)C#N)cc2o1 Show InChI InChI=1S/C20H13N3O3/c21-11-14-1-3-16(4-2-14)25-17-5-6-18-15(12-23-8-7-22-13-23)9-20(24)26-19(18)10-17/h1-10,13H,12H2	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	164	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339645 (7-[(3,4-Difluorobenzyl)oxy]-4-(1H-imidazol-1-ylmet...) Show SMILES Fc1ccc(COc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)cc1F Show InChI InChI=1S/C20H14F2N2O3/c21-17-4-1-13(7-18(17)22)11-26-15-2-3-16-14(10-24-6-5-23-12-24)8-20(25)27-19(16)9-15/h1-9,12H,10-11H2	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	165	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339644 (7-[(3,5-Difluorobenzyl)oxy]-4-(1H-imidazol-1-ylmet...) Show SMILES Fc1cc(F)cc(COc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)c1 Show InChI InChI=1S/C20H14F2N2O3/c21-15-5-13(6-16(22)8-15)11-26-17-1-2-18-14(10-24-4-3-23-12-24)7-20(25)27-19(18)9-17/h1-9,12H,10-11H2	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	169	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339641 (7-[(4-Chlorobenzyl)oxy]-4-(1H-imidazol-1-ylmethyl)...) Show SMILES Clc1ccc(COc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)cc1 Show InChI InChI=1S/C20H15ClN2O3/c21-16-3-1-14(2-4-16)12-25-17-5-6-18-15(11-23-8-7-22-13-23)9-20(24)26-19(18)10-17/h1-10,13H,11-12H2	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	178	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339668 (4-(1H-Imidazol-1-ylmethyl)-7-{[3-(trifluoromethoxy...) Show SMILES FC(F)(F)Oc1cccc(COc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)c1 Show InChI InChI=1S/C21H15F3N2O4/c22-21(23,24)30-17-3-1-2-14(8-17)12-28-16-4-5-18-15(11-26-7-6-25-13-26)9-20(27)29-19(18)10-16/h1-10,13H,11-12H2	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	207	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339667 (4-(1H-Imidazol-1-ylmethyl)-7-{[3-(trifluoromethyl)...) Show SMILES FC(F)(F)c1cccc(COc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)c1 Show InChI InChI=1S/C21H15F3N2O3/c22-21(23,24)16-3-1-2-14(8-16)12-28-17-4-5-18-15(11-26-7-6-25-13-26)9-20(27)29-19(18)10-17/h1-10,13H,11-12H2	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	235	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339640 (7-[(4-Fluorobenzyl)oxy]-4-(1H-imidazol-1-ylmethyl)...) Show SMILES Fc1ccc(COc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)cc1 Show InChI InChI=1S/C20H15FN2O3/c21-16-3-1-14(2-4-16)12-25-17-5-6-18-15(11-23-8-7-22-13-23)9-20(24)26-19(18)10-17/h1-10,13H,11-12H2	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	267	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM9471 (4-(1H-Imidazol-1-ylmethyl)-7-methoxy-2H-chromen-2-...) Show SMILES COc1ccc2c(Cn3ccnc3)cc(=O)oc2c1 Show InChI InChI=1S/C14H12N2O3/c1-18-11-2-3-12-10(8-16-5-4-15-9-16)6-14(17)19-13(12)7-11/h2-7,9H,8H2,1H3	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	280	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM9485 (7-(benzyloxy)-4-(1H-imidazol-1-ylmethyl)-2H-chrome...) Show SMILES O=c1cc(Cn2ccnc2)c2ccc(OCc3ccccc3)cc2o1 Show InChI InChI=1S/C20H16N2O3/c23-20-10-16(12-22-9-8-21-14-22)18-7-6-17(11-19(18)25-20)24-13-15-4-2-1-3-5-15/h1-11,14H,12-13H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	289	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human CYP11B2 expressed in Chinese hamster V79MZ cells using [1,2-3H]11-deoxycorticosterone/11-deoxycorticosterone				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339648 (4-(1H-Imidazol-1-ylmethyl)-7-(3-methoxyphenoxy)-2H...) Show SMILES COc1cccc(Oc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)c1 Show InChI InChI=1S/C20H16N2O4/c1-24-15-3-2-4-16(10-15)25-17-5-6-18-14(12-22-8-7-21-13-22)9-20(23)26-19(18)11-17/h2-11,13H,12H2,1H3	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	292	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339652 (7-(4-Acetylphenoxy)-4-(1H-imidazol-1-ylmethyl)-2H-...) Show SMILES CC(=O)c1ccc(Oc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)cc1 Show InChI InChI=1S/C21H16N2O4/c1-14(24)15-2-4-17(5-3-15)26-18-6-7-19-16(12-23-9-8-22-13-23)10-21(25)27-20(19)11-18/h2-11,13H,12H2,1H3	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	296	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339663 (CHEMBL1688919 | rac-3-[1H-Imidazol-1-yl(phenyl)met...) Show SMILES O=c1oc2cc(Oc3ccccc3)ccc2cc1C(c1ccccc1)n1ccnc1 Show InChI InChI=1S/C25H18N2O3/c28-25-22(24(27-14-13-26-17-27)18-7-3-1-4-8-18)15-19-11-12-21(16-23(19)30-25)29-20-9-5-2-6-10-20/h1-17,24H	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	313	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339660 (CHEMBL1688916 | rac-7-(3,4-Difluorophenoxy)-4-[1H-...) Show SMILES Fc1ccc(Oc2ccc3c(cc(=O)oc3c2)C(c2ccccc2)n2ccnc2)cc1F Show InChI InChI=1S/C25H16F2N2O3/c26-21-9-7-17(12-22(21)27)31-18-6-8-19-20(14-24(30)32-23(19)13-18)25(29-11-10-28-15-29)16-4-2-1-3-5-16/h1-15,25H	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	317	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339658 (CHEMBL1688914 | rac-4-[1H-Imidazol-1-yl(phenyl)met...) Show SMILES COc1ccc2c(cc(=O)oc2c1)C(c1ccccc1)n1ccnc1 Show InChI InChI=1S/C20H16N2O3/c1-24-15-7-8-16-17(12-19(23)25-18(16)11-15)20(22-10-9-21-13-22)14-5-3-2-4-6-14/h2-13,20H,1H3	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	455	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339643 (4-(1H-Imidazol-1-ylmethyl)-7-[(4-trifluoromethoxyb...) Show SMILES FC(F)(F)Oc1ccc(COc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)cc1 Show InChI InChI=1S/C21H15F3N2O4/c22-21(23,24)30-16-3-1-14(2-4-16)12-28-17-5-6-18-15(11-26-8-7-25-13-26)9-20(27)29-19(18)10-17/h1-10,13H,11-12H2	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	481	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339661 (CHEMBL1688917 | rac-4-[(4-Chlorophenyl)(1H-imidazo...) Show SMILES Clc1ccc(cc1)C(c1cc(=O)oc2cc(Oc3ccccc3)ccc12)n1ccnc1 Show InChI InChI=1S/C25H17ClN2O3/c26-18-8-6-17(7-9-18)25(28-13-12-27-16-28)22-15-24(29)31-23-14-20(10-11-21(22)23)30-19-4-2-1-3-5-19/h1-16,25H	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	532	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339649 (4-(1H-Imidazol-1-ylmethyl)-7-(4-methylphenoxy)-2H-...) Show SMILES Cc1ccc(Oc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)cc1 Show InChI InChI=1S/C20H16N2O3/c1-14-2-4-16(5-3-14)24-17-6-7-18-15(12-22-9-8-21-13-22)10-20(23)25-19(18)11-17/h2-11,13H,12H2,1H3	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	690	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Cytochrome P450 11B1, mitochondrial (Homo sapiens (Human))	BDBM50339655 (7-(3,4-Difluorophenoxy)-4-(1H-imidazol-1-ylmethyl)...) Show SMILES Fc1ccc(Oc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)cc1F Show InChI InChI=1S/C19H12F2N2O3/c20-16-4-2-13(8-17(16)21)25-14-1-3-15-12(10-23-6-5-22-11-23)7-19(24)26-18(15)9-14/h1-9,11H,10H2	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	933	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human CYP11B1 expressed in Chinese hamster V79MZ cells using [1,2-3H]11-deoxycorticosterone/11-deoxycorticosterone				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM50339655 (7-(3,4-Difluorophenoxy)-4-(1H-imidazol-1-ylmethyl)...) Show SMILES Fc1ccc(Oc2ccc3c(Cn4ccnc4)cc(=O)oc3c2)cc1F Show InChI InChI=1S/C19H12F2N2O3/c20-16-4-2-13(8-17(16)21)25-14-1-3-15-12(10-23-6-5-22-11-23)7-19(24)26-18(15)9-14/h1-9,11H,10H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.19E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human CYP11B2 expressed in Chinese hamster V79MZ cells using [1,2-3H]11-deoxycorticosterone/11-deoxycorticosterone				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM9469 (3-(1H-Imidazol-1-ylmethyl)-7-methoxy-2H-chromen-2-...) Show SMILES COc1ccc2cc(Cn3ccnc3)c(=O)oc2c1 Show InChI InChI=1S/C14H12N2O3/c1-18-12-3-2-10-6-11(8-16-5-4-15-9-16)14(17)19-13(10)7-12/h2-7,9H,8H2,1H3	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	2.82E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339657 (7-Hydroxy-4-(1H-Imidazol-1-ylmethyl)-2H-chromen-2-...) Show SMILES Oc1ccc2c(Cn3ccnc3)cc(=O)oc2c1 Show InChI InChI=1S/C13H10N2O3/c16-10-1-2-11-9(7-15-4-3-14-8-15)5-13(17)18-12(11)6-10/h1-6,8,16H,7H2	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	3.75E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM50339662 (CHEMBL1688918 | rac-4-[1H-Imidazol-1-yl(2-oxo-7-ph...) Show SMILES O=c1cc(C(c2ccc(cc2)C#N)n2ccnc2)c2ccc(Oc3ccccc3)cc2o1 Show InChI InChI=1S/C26H17N3O3/c27-16-18-6-8-19(9-7-18)26(29-13-12-28-17-29)23-15-25(30)32-24-14-21(10-11-22(23)24)31-20-4-2-1-3-5-20/h1-15,17,26H	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	4.01E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair
Steroid 17-alpha-hydroxylase/17,20 lyase (Homo sapiens (Human))	BDBM31768 (CHEMBL295698 | Ketoconazole | Nizoral | Panfungol) Show SMILES CC(=O)N1CCN(CC1)c1ccc(OC[C@@H]2CO[C@](Cn3ccnc3)(O2)c2ccc(Cl)cc2Cl)cc1 |r| Show InChI InChI=1S/C26H28Cl2N4O4/c1-19(33)31-10-12-32(13-11-31)21-3-5-22(6-4-21)34-15-23-16-35-26(36-23,17-30-9-8-29-18-30)24-7-2-20(27)14-25(24)28/h2-9,14,18,23H,10-13,15-17H2,1H3/t23-,26-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	4.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Bari Aldo Moro Curated by ChEMBL					Assay Description Inhibition of human CYP17 expressed in Escherichia coli using progesterone as a substrate				J Med Chem 54: 1613-25 (2011) Article DOI: 10.1021/jm101120u BindingDB Entry DOI: 10.7270/Q24X583Q
					More data for this Ligand-Target Pair