Compile Data Set for Download or QSAR
Report error Found 3477 Enz. Inhib. hit(s) with Target = 'Aromatase'
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM9991((2S,6S,15S)-6-hydroxy-2-(methoxymethyl)-15-methylt...)
Affinity DatapH: 7.5 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta-3H] Androstenedione during aromatization. After incubation, the re...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM8938(dihydronaphthalene derivative | 7-(1H-Imidazol-5-y...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/1/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM8939(4-({9-methoxy-2-methyl-3-oxatricyclo[5.4.0.0^{2,4}...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/1/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM8947(6,7-Dihydroxy-2-(1H-imidazol-5-ylmethyl)-3,4-dihyd...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/1/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM8948(1-{[4-(3-methoxyphenyl)phenyl]methyl}-1H-imidazole...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/1/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM8949(3-[4-(1H-imidazol-1-ylmethyl)phenyl]phenol | methy...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/1/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM8950(2-[4-(1H-imidazol-1-ylmethyl)phenyl]benzene-1,4-di...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/1/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM8952(4-[4-(1H-imidazol-1-ylmethyl)phenyl]benzene-1,2,3-...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/1/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM8954(1-{[4-(2,5-dimethoxyphenyl)phenyl]methyl}-1H-imida...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/1/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM8955(1-[(3,4-dimethoxy-1,1-biphenyl-4-yl)methyl]-1H-imi...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/1/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM8957(1-{[4-(3,4,5-trimethoxyphenyl)phenyl]methyl}-1H-im...)
Affinity DataAssay Description:The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/1/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM9466(4-(9-Phenyl-9H-fluoren-9-yl)-4H-1,2,4-triazole | F...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM9467(1-(9-Phenyl-9H-fluoren-9-yl)-1H-1,2,3-triazole | F...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM9474(4-[2-(1H-Imidazol-1-yl)ethoxy]-7-methoxy-2H-chrome...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM9479(7-(1H-1,2,4-Triazol-1-ylmethyl)-2H-chromen-2-one |...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM9480(7-[2-(1H-Imidazol-1-yl)ethoxy]-2H-chromen-2-one | ...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM9481(8-(1H-Imidazol-1-ylmethyl)-7-methoxy-2H-chromen-2-...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM9484(7-methoxy-4-(pyridin-4-yl)-2H-chromen-2-one | Coum...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta, 2beta-3H] testosterone or [1beta-3H] androstenedione during aroma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2006
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM24302((2-methoxy-5-{[4-methoxy-3-(sulfamoyloxy)phenyl](1...)
Affinity DatapH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/14/2008
Entry Details Article
PubMed
TargetAromatase(Human)
Tohoku Pharmaceutical University

LigandPNGBDBM24303((2-methoxy-4-{[3-methoxy-4-(sulfamoyloxy)phenyl](1...)
Affinity DatapH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/14/2008
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024479((4-Chloro-phenyl)-cyclopropyl-pyrimidin-5-yl-metha...)
Affinity DataEC50:  5.70E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024480((3,4-Dichloro-phenyl)-phenyl-pyrimidin-5-yl-methan...)
Affinity DataEC50:  1.00E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024481((4-Chloro-phenyl)-pyrimidin-5-yl-(4-trifluoromethy...)
Affinity DataEC50:  66nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024482(Phenyl-pyrimidin-5-yl-(4-trifluoromethyl-phenyl)-m...)
Affinity DataEC50:  1.95E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024483((4-Nitro-phenyl)-phenyl-pyrimidin-5-yl-methanol | ...)
Affinity DataEC50:  270nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024484(5-[1,1,2-Tris-(4-chloro-phenyl)-ethyl]-pyrimidine ...)
Affinity DataEC50: >2.00E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024485(5-[1,1-Bis-(4-chloro-phenyl)-2-phenyl-ethyl]-pyrim...)
Affinity DataEC50:  1.01E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024486(Bis-(4-chloro-phenyl)-(1-oxy-pyrimidin-5-yl)-metha...)
Affinity DataEC50: >2.00E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024487(1-(4-Chloro-phenyl)-2-methyl-1-pyrimidin-5-yl-prop...)
Affinity DataEC50: >2.00E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024489(5-[Bis-(4-chloro-phenyl)-methylene]-1,4,5,6-tetrah...)
Affinity DataEC50:  2.70E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024490(5-[Chloro-bis-(4-chloro-phenyl)-methyl]-pyrimidine...)
Affinity DataEC50:  275nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024488(Bis-(4-fluoro-phenyl)-pyrimidin-5-yl-methanol | CH...)
Affinity DataEC50:  530nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM9460(3-(4-aminophenyl)-3-ethyl-piperidine-2,6-dione | C...)
Affinity DataEC50:  260nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM31772(Brentan | 1-[2-(2,4-dichlorobenzyl)oxy-2-(2,4-dich...)
Affinity DataEC50:  400nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024491(5-[(2-Chloro-phenyl)-fluoro-(4-fluoro-phenyl)-meth...)
Affinity DataEC50:  1.20E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024492(Diphenyl-pyrimidin-5-yl-methanol | CHEMBL29670)
Affinity DataEC50: >2.00E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50014324(CHEMBL29669 | 5-[Bis-(4-chloro-phenyl)-methyl]-pyr...)
Affinity DataEC50:  55nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024494((4-Fluoro-phenyl)-phenyl-pyrimidin-5-yl-methanol |...)
Affinity DataEC50: >2.20E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024493(Cyclopropyl-(4-fluoro-phenyl)-pyrimidin-5-yl-metha...)
Affinity DataEC50:  4.20E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024495(Pyrimidin-5-yl-di-p-tolyl-methanol | CHEMBL283085)
Affinity DataEC50:  410nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024497(2-Methyl-1-(5-methyl-thiophen-2-yl)-1-pyrimidin-5-...)
Affinity DataEC50: >2.00E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024496(Pyrimidin-5-yl-di-thiophen-2-yl-methanol | CHEMBL2...)
Affinity DataEC50: >2.00E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024498(5-[1,1-Bis-(4-chloro-phenyl)-propyl]-pyrimidine | ...)
Affinity DataEC50:  2.95E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024499(1-(4-Methoxy-phenyl)-2-methyl-1-pyrimidin-5-yl-but...)
Affinity DataEC50: >2.00E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024500(Phenyl-pyrimidin-5-yl-thiophen-2-yl-methanol | CHE...)
Affinity DataEC50: >2.00E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024501((4-Bromo-phenyl)-cyclopropyl-pyrimidin-5-yl-methan...)
Affinity DataEC50:  5.40E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024502(1-(4-Methoxy-phenyl)-2,2-dimethyl-1-pyrimidin-5-yl...)
Affinity DataEC50: >2.00E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024503(Cyclopropyl-pyrimidin-5-yl-thiophen-2-yl-methanol ...)
Affinity DataEC50: >2.00E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024504((2-Chloro-4-methoxy-phenyl)-(4-chloro-phenyl)-pyri...)
Affinity DataEC50:  4.30E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAromatase(Rat)
TBA

Curated by ChEMBL
LigandPNGBDBM50024506((4-Chloro-phenyl)-phenyl-pyrimidin-5-yl-methanol |...)
Affinity DataEC50: >2.00E+3nMAssay Description:In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
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