Compile Data Set for Download or QSAR

Found 131 hits of affinity data for UniProtKB/TrEMBL: P22443   

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 (Rattus norvegicus)	BDBM50136199 (CHEMBL3349548) Show SMILES [H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])[C@@H](CC2=CC(=O)C=C[C@]12C)Sc1ccc(N)cc1 |c:22,t:18| Show InChI InChI=1S/C25H29NO2S/c1-24-11-9-17(27)13-15(24)14-21(29-18-5-3-16(26)4-6-18)23-19-7-8-22(28)25(19,2)12-10-20(23)24/h3-6,9,11,13,19-21,23H,7-8,10,12,14,26H2,1-2H3/t19-,20-,21+,23-,24-,25-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	18	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1016/j.ejmech.2022.114658 BindingDB Entry DOI: 10.7270/Q2NP28CD
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50014320 (8-Chloro-5-(4-chloro-phenyl)-5H-indeno[1,2-d]pyrim...) Show SMILES Clc1ccc(cc1)C1c2ccc(Cl)cc2-c2ncncc12 Show InChI InChI=1S/C17H10Cl2N2/c18-11-3-1-10(2-4-11)16-13-6-5-12(19)7-14(13)17-15(16)8-20-9-21-17/h1-9,16H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	PubMed	24	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johns Hopkins University School of Medicine Curated by ChEMBL					Assay Description Binding affinity for Cytochrome P450 19A1				J Med Chem 33: 2933-42 (1990) BindingDB Entry DOI: 10.7270/Q2VM4CW9
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50014324 (5-[Bis-(4-chloro-phenyl)-methyl]-pyrimidine | 5-[B...) Show SMILES Clc1ccc(cc1)C(c1ccc(Cl)cc1)c1cncnc1 Show InChI InChI=1S/C17H12Cl2N2/c18-15-5-1-12(2-6-15)17(14-9-20-11-21-10-14)13-3-7-16(19)8-4-13/h1-11,17H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	PubMed	29	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johns Hopkins University School of Medicine Curated by ChEMBL					Assay Description Binding affinity for Cytochrome P450 19A1				J Med Chem 33: 2933-42 (1990) BindingDB Entry DOI: 10.7270/Q2VM4CW9
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50014315 ((rac)-6-((4-chlorophenyl)(1H-1,2,4-triazol-1-yl)me...) Show SMILES Cn1nnc2ccc(cc12)C(c1ccc(Cl)cc1)n1cncn1 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	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Johns Hopkins University School of Medicine Curated by ChEMBL					Assay Description Binding affinity for Cytochrome P450 19A1				J Med Chem 33: 2933-42 (1990) BindingDB Entry DOI: 10.7270/Q2VM4CW9
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	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)	Reactome pathway KEGG UniProtKB/SwissProt 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
American University of Ras Al Khaimah Curated by ChEMBL					Assay Description Inhibition of rat ovarian aromatase				Eur J Med Chem 102: 375-86 (2015) Article DOI: 10.1016/j.ejmech.2015.08.010 BindingDB Entry DOI: 10.7270/Q2ZC84Q6
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50123022 (CHEMBL169251) Show SMILES O=C1\C(CCc2ccccc12)=C/c1c[nH]cn1 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)/b11-7-	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a	n/a
American University of Ras Al Khaimah Curated by ChEMBL					Assay Description Inhibition of rat ovarian aromatase				Eur J Med Chem 102: 375-86 (2015) Article DOI: 10.1016/j.ejmech.2015.08.010 BindingDB Entry DOI: 10.7270/Q2ZC84Q6
					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 (Rattus norvegicus)	BDBM50009606 (5-Hydroxy-2-pyridin-4-ylmethyl-3,4-dihydro-2H-naph...) Show SMILES Oc1cccc2C(=O)C(Cc3ccncc3)CCc12 Show InChI InChI=1S/C16H15NO2/c18-15-3-1-2-14-13(15)5-4-12(16(14)19)10-11-6-8-17-9-7-11/h1-3,6-9,12,18H,4-5,10H2	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.00E+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 rat ovarian aromatase cytochrome P450 19A1				J Med Chem 34: 2685-91 (1991) BindingDB Entry DOI: 10.7270/Q2ST7NT9
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	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+	Reactome pathway KEGG UniProtKB/SwissProt 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
American University of Ras Al Khaimah Curated by ChEMBL					Assay Description Inhibition of rat ovarian aromatase				Eur J Med Chem 102: 375-86 (2015) Article DOI: 10.1016/j.ejmech.2015.08.010 BindingDB Entry DOI: 10.7270/Q2ZC84Q6
					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
Aromatase (Rattus norvegicus)	BDBM50009618 (5-Methoxy-2-pyridin-4-ylmethyl-3,4-dihydro-2H-naph...) Show SMILES COc1cccc2C(=O)C(Cc3ccncc3)CCc12 Show InChI InChI=1S/C17H17NO2/c1-20-16-4-2-3-15-14(16)6-5-13(17(15)19)11-12-7-9-18-10-8-12/h2-4,7-10,13H,5-6,11H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	8.00E+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 rat ovarian aromatase cytochrome P450 19A1				J Med Chem 34: 2685-91 (1991) BindingDB Entry DOI: 10.7270/Q2ST7NT9
					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	3.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universität des Saarlandes Curated by ChEMBL					Assay Description Inhibition of rat ovarian Cytochrome P450 19A				J Med Chem 34: 2685-91 (1991) BindingDB Entry DOI: 10.7270/Q2ST7NT9
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024479 ((4-Chloro-phenyl)-cyclopropyl-pyrimidin-5-yl-metha...) Show SMILES OC(C1CC1)(c1ccc(Cl)cc1)c1cncnc1 Show InChI InChI=1S/C14H13ClN2O/c15-13-5-3-11(4-6-13)14(18,10-1-2-10)12-7-16-9-17-8-12/h3-10,18H,1-2H2	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	5.70E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024480 ((3,4-Dichloro-phenyl)-phenyl-pyrimidin-5-yl-methan...) Show SMILES OC(c1ccccc1)(c1ccc(Cl)c(Cl)c1)c1cncnc1 Show InChI InChI=1S/C17H12Cl2N2O/c18-15-7-6-13(8-16(15)19)17(22,12-4-2-1-3-5-12)14-9-20-11-21-10-14/h1-11,22H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024481 ((4-Chloro-phenyl)-pyrimidin-5-yl-(4-trifluoromethy...) Show SMILES OC(c1ccc(Cl)cc1)(c1ccc(cc1)C(F)(F)F)c1cncnc1 Show InChI InChI=1S/C18H12ClF3N2O/c19-16-7-5-13(6-8-16)17(25,15-9-23-11-24-10-15)12-1-3-14(4-2-12)18(20,21)22/h1-11,25H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	66	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024482 (CHEMBL284636 | Phenyl-pyrimidin-5-yl-(4-trifluorom...) Show SMILES OC(c1ccccc1)(c1ccc(cc1)C(F)(F)F)c1cncnc1 Show InChI InChI=1S/C18H13F3N2O/c19-18(20,21)15-8-6-14(7-9-15)17(24,13-4-2-1-3-5-13)16-10-22-12-23-11-16/h1-12,24H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	1.95E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024483 ((4-Nitro-phenyl)-phenyl-pyrimidin-5-yl-methanol | ...) Show SMILES OC(c1ccccc1)(c1ccc(cc1)[N+]([O-])=O)c1cncnc1 Show InChI InChI=1S/C17H13N3O3/c21-17(13-4-2-1-3-5-13,15-10-18-12-19-11-15)14-6-8-16(9-7-14)20(22)23/h1-12,21H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	n/a	n/a	270	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024484 (5-[1,1,2-Tris-(4-chloro-phenyl)-ethyl]-pyrimidine ...) Show SMILES Clc1ccc(CC(c2ccc(Cl)cc2)(c2ccc(Cl)cc2)c2cncnc2)cc1 Show InChI InChI=1S/C24H17Cl3N2/c25-21-7-1-17(2-8-21)13-24(20-14-28-16-29-15-20,18-3-9-22(26)10-4-18)19-5-11-23(27)12-6-19/h1-12,14-16H,13H2	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024485 (5-[1,1-Bis-(4-chloro-phenyl)-2-phenyl-ethyl]-pyrim...) Show SMILES Clc1ccc(cc1)C(Cc1ccccc1)(c1ccc(Cl)cc1)c1cncnc1 Show InChI InChI=1S/C24H18Cl2N2/c25-22-10-6-19(7-11-22)24(21-15-27-17-28-16-21,14-18-4-2-1-3-5-18)20-8-12-23(26)13-9-20/h1-13,15-17H,14H2	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	1.01E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024486 (Bis-(4-chloro-phenyl)-(1-oxy-pyrimidin-5-yl)-metha...) Show SMILES OC(c1ccc(Cl)cc1)(c1ccc(Cl)cc1)c1cnc[n+]([O-])c1 Show InChI InChI=1S/C17H12Cl2N2O2/c18-15-5-1-12(2-6-15)17(22,13-3-7-16(19)8-4-13)14-9-20-11-21(23)10-14/h1-11,22H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024487 (1-(4-Chloro-phenyl)-2-methyl-1-pyrimidin-5-yl-prop...) Show SMILES CC(C)C(O)(c1ccc(Cl)cc1)c1cncnc1 Show InChI InChI=1S/C14H15ClN2O/c1-10(2)14(18,12-7-16-9-17-8-12)11-3-5-13(15)6-4-11/h3-10,18H,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024489 (5-[Bis-(4-chloro-phenyl)-methylene]-1,4,5,6-tetrah...) Show SMILES Clc1ccc(cc1)C(=C1CNC=NC1)c1ccc(Cl)cc1 |c:12| Show InChI InChI=1S/C17H14Cl2N2/c18-15-5-1-12(2-6-15)17(14-9-20-11-21-10-14)13-3-7-16(19)8-4-13/h1-8,11H,9-10H2,(H,20,21)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	n/a	n/a	2.70E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024490 (5-[Chloro-bis-(4-chloro-phenyl)-methyl]-pyrimidine...) Show SMILES Clc1ccc(cc1)C(Cl)(c1ccc(Cl)cc1)c1cncnc1 Show InChI InChI=1S/C17H11Cl3N2/c18-15-5-1-12(2-6-15)17(20,14-9-21-11-22-10-14)13-3-7-16(19)8-4-13/h1-11H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	275	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024488 (Bis-(4-fluoro-phenyl)-pyrimidin-5-yl-methanol | CH...) Show SMILES OC(c1ccc(F)cc1)(c1ccc(F)cc1)c1cncnc1 Show InChI InChI=1S/C17H12F2N2O/c18-15-5-1-12(2-6-15)17(22,14-9-20-11-21-10-14)13-3-7-16(19)8-4-13/h1-11,22H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	530	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					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	n/a	n/a	260	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM31772 (1-[2-(2,4-dichlorobenzyl)oxy-2-(2,4-dichlorophenyl...) Show SMILES Clc1ccc(COC(Cn2ccnc2)c2ccc(Cl)cc2Cl)c(Cl)c1 Show InChI InChI=1S/C18H14Cl4N2O/c19-13-2-1-12(16(21)7-13)10-25-18(9-24-6-5-23-11-24)15-4-3-14(20)8-17(15)22/h1-8,11,18H,9-10H2	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	400	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024491 (5-[(2-Chloro-phenyl)-fluoro-(4-fluoro-phenyl)-meth...) Show SMILES Fc1ccc(cc1)C(F)(c1cncnc1)c1ccccc1Cl Show InChI InChI=1S/C17H11ClF2N2/c18-16-4-2-1-3-15(16)17(20,13-9-21-11-22-10-13)12-5-7-14(19)8-6-12/h1-11H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024492 (CHEMBL29670 | Diphenyl-pyrimidin-5-yl-methanol) Show SMILES OC(c1ccccc1)(c1ccccc1)c1cncnc1 Show InChI InChI=1S/C17H14N2O/c20-17(14-7-3-1-4-8-14,15-9-5-2-6-10-15)16-11-18-13-19-12-16/h1-13,20H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50014324 (5-[Bis-(4-chloro-phenyl)-methyl]-pyrimidine | 5-[B...) Show SMILES Clc1ccc(cc1)C(c1ccc(Cl)cc1)c1cncnc1 Show InChI InChI=1S/C17H12Cl2N2/c18-15-5-1-12(2-6-15)17(14-9-20-11-21-10-14)13-3-7-16(19)8-4-13/h1-11,17H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	55	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024494 ((4-Fluoro-phenyl)-phenyl-pyrimidin-5-yl-methanol |...) Show SMILES OC(c1ccccc1)(c1ccc(F)cc1)c1cncnc1 Show InChI InChI=1S/C17H13FN2O/c18-16-8-6-14(7-9-16)17(21,13-4-2-1-3-5-13)15-10-19-12-20-11-15/h1-12,21H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	>2.20E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024493 (CHEMBL30081 | Cyclopropyl-(4-fluoro-phenyl)-pyrimi...) Show SMILES OC(C1CC1)(c1ccc(F)cc1)c1cncnc1 Show InChI InChI=1S/C14H13FN2O/c15-13-5-3-11(4-6-13)14(18,10-1-2-10)12-7-16-9-17-8-12/h3-10,18H,1-2H2	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	4.20E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024495 (CHEMBL283085 | Pyrimidin-5-yl-di-p-tolyl-methanol) Show SMILES Cc1ccc(cc1)C(O)(c1ccc(C)cc1)c1cncnc1 Show InChI InChI=1S/C19H18N2O/c1-14-3-7-16(8-4-14)19(22,18-11-20-13-21-12-18)17-9-5-15(2)6-10-17/h3-13,22H,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	410	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024497 (2-Methyl-1-(5-methyl-thiophen-2-yl)-1-pyrimidin-5-...) Show SMILES CC(C)C(O)(c1ccc(C)s1)c1cncnc1 Show InChI InChI=1S/C13H16N2OS/c1-9(2)13(16,11-6-14-8-15-7-11)12-5-4-10(3)17-12/h4-9,16H,1-3H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024496 (CHEMBL29412 | Pyrimidin-5-yl-di-thiophen-2-yl-meth...) Show SMILES OC(c1cccs1)(c1cccs1)c1cncnc1 Show InChI InChI=1S/C13H10N2OS2/c16-13(11-3-1-5-17-11,12-4-2-6-18-12)10-7-14-9-15-8-10/h1-9,16H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024498 (5-[1,1-Bis-(4-chloro-phenyl)-propyl]-pyrimidine | ...) Show SMILES CCC(c1ccc(Cl)cc1)(c1ccc(Cl)cc1)c1cncnc1 Show InChI InChI=1S/C19H16Cl2N2/c1-2-19(16-11-22-13-23-12-16,14-3-7-17(20)8-4-14)15-5-9-18(21)10-6-15/h3-13H,2H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	2.95E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024499 (1-(4-Methoxy-phenyl)-2-methyl-1-pyrimidin-5-yl-but...) Show SMILES CCC(C)C(O)(c1ccc(OC)cc1)c1cncnc1 Show InChI InChI=1S/C16H20N2O2/c1-4-12(2)16(19,14-9-17-11-18-10-14)13-5-7-15(20-3)8-6-13/h5-12,19H,4H2,1-3H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024500 (CHEMBL29140 | Phenyl-pyrimidin-5-yl-thiophen-2-yl-...) Show SMILES OC(c1cccs1)(c1ccccc1)c1cncnc1 Show InChI InChI=1S/C15H12N2OS/c18-15(14-7-4-8-19-14,12-5-2-1-3-6-12)13-9-16-11-17-10-13/h1-11,18H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024501 ((4-Bromo-phenyl)-cyclopropyl-pyrimidin-5-yl-methan...) Show SMILES OC(C1CC1)(c1ccc(Br)cc1)c1cncnc1 Show InChI InChI=1S/C14H13BrN2O/c15-13-5-3-11(4-6-13)14(18,10-1-2-10)12-7-16-9-17-8-12/h3-10,18H,1-2H2	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	n/a	n/a	5.40E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024502 (1-(4-Methoxy-phenyl)-2,2-dimethyl-1-pyrimidin-5-yl...) Show SMILES COc1ccc(cc1)C(O)(c1cncnc1)C(C)(C)C Show InChI InChI=1S/C16H20N2O2/c1-15(2,3)16(19,13-9-17-11-18-10-13)12-5-7-14(20-4)8-6-12/h5-11,19H,1-4H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024503 (CHEMBL28860 | Cyclopropyl-pyrimidin-5-yl-thiophen-...) Show SMILES OC(C1CC1)(c1cccs1)c1cncnc1 Show InChI InChI=1S/C12H12N2OS/c15-12(9-3-4-9,11-2-1-5-16-11)10-6-13-8-14-7-10/h1-2,5-9,15H,3-4H2	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024504 ((2-Chloro-4-methoxy-phenyl)-(4-chloro-phenyl)-pyri...) Show SMILES COc1ccc(c(Cl)c1)C(O)(c1ccc(Cl)cc1)c1cncnc1 Show InChI InChI=1S/C18H14Cl2N2O2/c1-24-15-6-7-16(17(20)8-15)18(23,13-9-21-11-22-10-13)12-2-4-14(19)5-3-12/h2-11,23H,1H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	n/a	n/a	4.30E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024506 ((4-Chloro-phenyl)-phenyl-pyrimidin-5-yl-methanol |...) Show SMILES OC(c1ccccc1)(c1ccc(Cl)cc1)c1cncnc1 Show InChI InChI=1S/C17H13ClN2O/c18-16-8-6-14(7-9-16)17(21,13-4-2-1-3-5-13)15-10-19-12-20-11-15/h1-12,21H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024505 ((3,4-Dimethyl-phenyl)-(4-methoxy-3-methyl-phenyl)-...) Show SMILES COc1ccc(cc1C)C(O)(c1ccc(C)c(C)c1)c1cncnc1 Show InChI InChI=1S/C21H22N2O2/c1-14-5-6-17(9-15(14)2)21(24,19-11-22-13-23-12-19)18-7-8-20(25-4)16(3)10-18/h5-13,24H,1-4H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024507 ((3,4-Dimethyl-phenyl)-phenyl-pyrimidin-5-yl-methan...) Show SMILES Cc1ccc(cc1C)C(O)(c1ccccc1)c1cncnc1 Show InChI InChI=1S/C19H18N2O/c1-14-8-9-17(10-15(14)2)19(22,16-6-4-3-5-7-16)18-11-20-13-21-12-18/h3-13,22H,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	3.20E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024512 (CHEMBL280781 | Cyclohexyl-pyrimidin-5-yl-p-tolyl-m...) Show SMILES Cc1ccc(cc1)C(O)(C1CCCCC1)c1cncnc1 Show InChI InChI=1S/C18H22N2O/c1-14-7-9-16(10-8-14)18(21,15-5-3-2-4-6-15)17-11-19-13-20-12-17/h7-13,15,21H,2-6H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024511 ((4-Chloro-phenyl)-(2-chloro-phenyl)-pyrimidin-5-yl...) Show SMILES OC(c1ccc(Cl)cc1)(c1cncnc1)c1ccccc1Cl Show InChI InChI=1S/C17H12Cl2N2O/c18-14-7-5-12(6-8-14)17(22,13-9-20-11-21-10-13)15-3-1-2-4-16(15)19/h1-11,22H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	4.10E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024508 (5-[(4-Chloro-phenyl)-fluoro-(4-fluoro-phenyl)-meth...) Show SMILES Fc1ccc(cc1)C(F)(c1ccc(Cl)cc1)c1cncnc1 Show InChI InChI=1S/C17H11ClF2N2/c18-15-5-1-12(2-6-15)17(20,14-9-21-11-22-10-14)13-3-7-16(19)8-4-13/h1-11H	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	195	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024510 (CHEMBL417120 | Cyclopentyl-cyclopropyl-pyrimidin-5...) Show SMILES OC(C1CC1)(C1CCCC1)c1cncnc1 Show InChI InChI=1S/C13H18N2O/c16-13(11-5-6-11,10-3-1-2-4-10)12-7-14-9-15-8-12/h7-11,16H,1-6H2	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024509 (CHEMBL285844 | Cyclobutyl-(4-methoxy-phenyl)-pyrim...) Show SMILES COc1ccc(cc1)C(O)(C1CCC1)c1cncnc1 Show InChI InChI=1S/C16H18N2O2/c1-20-15-7-5-13(6-8-15)16(19,12-3-2-4-12)14-9-17-11-18-10-14/h5-12,19H,2-4H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair
Aromatase (Rattus norvegicus)	BDBM50024513 (6-Acetylsulfanyl-8-[2-[(4-amino-2-methyl-pyrimidin...) Show SMILES COC(=O)CCCCC(CCSS\C(CCO)=C(/C)N(Cc1cnc(C)nc1N)C=O)SC(C)=O Show InChI InChI=1S/C23H36N4O5S3/c1-16(27(15-29)14-19-13-25-17(2)26-23(19)24)21(9-11-28)35-33-12-10-20(34-18(3)30)7-5-6-8-22(31)32-4/h13,15,20,28H,5-12,14H2,1-4H3,(H2,24,25,26)/b21-16+	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem	PubMed	n/a	n/a	n/a	n/a	140	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.				J Med Chem 30: 1359-65 (1987) BindingDB Entry DOI: 10.7270/Q2NP251P
					More data for this Ligand-Target Pair

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