Compile Data Set for Download or QSAR
Found 9 from University of Oporto
TargetAromatase(Homo sapiens (Human))
University of Oporto

Curated by ChEMBL
LigandPNGBDBM50174541((3R,4S,5R,10R,13S)-10,13-Dimethyl-hexadecahydro-20...)copy SMILEScopy InChI
Affinity DataKi:  38nMAssay Description:Inhibition constant against aromatase protein from human placental microsomes using [1-beta-3H]-androstenedione; Competitive inhibitionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M66GDPubMed
TargetAromatase(Homo sapiens (Human))
University of Oporto

Curated by ChEMBL
LigandPNGBDBM50174544((5S,10S,13S)-10,13-Dimethyl-1,2,5,6,7,8,9,10,11,12...)copy SMILEScopy InChI
Affinity DataKi:  50nMAssay Description:Inhibition constant against aromatase protein from human placental microsomes using [1-beta-3H]-androstenedione; Competitive inhibitionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M66GDPubMed
TargetAromatase(Homo sapiens (Human))
University of Oporto

Curated by ChEMBL
LigandPNGBDBM50174543((3R,5R,10R,13S)-3-Hydroxy-10,13-dimethyl-tetradeca...)copy SMILEScopy InChI
Affinity DataKi:  147nMAssay Description:Inhibition constant against aromatase protein from human placental microsomes using [1-beta-3H]-androstenedione; Competitive inhibitionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M66GDPubMed
TargetAromatase(Homo sapiens (Human))
University of Oporto

Curated by ChEMBL
LigandPNGBDBM50174542((10aR,12aS)-7-Hydroxy-10a,12a-dimethyl-3,4,4a,5,6,...)copy SMILEScopy InChI
Affinity DataKi:  660nMAssay Description:Inhibition constant against aromatase protein from human placental microsomes using [1-beta-3H]-androstenedione; Competitive inhibitionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M66GDPubMed
TargetAromatase(Homo sapiens (Human))
University of Oporto

Curated by ChEMBL
LigandPNGBDBM50240798((8R,9S,10R,13S,14S)-4-Hydroxy-10,13-dimethyl-1,6,7...)copy SMILEScopy InChI
Affinity DataIC50: 42nMAssay Description:Inhibitory concentration against aromatase protein from human placental microsomes using [1-beta-3H]-androstenedione; Competitive inhibitionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M66GDPubMed
TargetAromatase(Homo sapiens (Human))
University of Oporto

Curated by ChEMBL
LigandPNGBDBM50174541((3R,4S,5R,10R,13S)-10,13-Dimethyl-hexadecahydro-20...)copy SMILEScopy InChI
Affinity DataIC50: 145nMAssay Description:Inhibitory concentration against aromatase protein from human placental microsomes using [1-beta-3H]-androstenedione; Competitive inhibitionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M66GDPubMed
TargetAromatase(Homo sapiens (Human))
University of Oporto

Curated by ChEMBL
LigandPNGBDBM50174544((5S,10S,13S)-10,13-Dimethyl-1,2,5,6,7,8,9,10,11,12...)copy SMILEScopy InChI
Affinity DataIC50: 225nMAssay Description:Inhibitory concentration against aromatase protein from human placental microsomes using [1-beta-3H]-androstenedione; Competitive inhibitionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M66GDPubMed
TargetAromatase(Homo sapiens (Human))
University of Oporto

Curated by ChEMBL
LigandPNGBDBM50174543((3R,5R,10R,13S)-3-Hydroxy-10,13-dimethyl-tetradeca...)copy SMILEScopy InChI
Affinity DataIC50: 670nMAssay Description:Inhibitory concentration against aromatase protein from human placental microsomes using [1-beta-3H]-androstenedione; Competitive inhibitionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M66GDPubMed
TargetAromatase(Homo sapiens (Human))
University of Oporto

Curated by ChEMBL
LigandPNGBDBM50174542((10aR,12aS)-7-Hydroxy-10a,12a-dimethyl-3,4,4a,5,6,...)copy SMILEScopy InChI
Affinity DataIC50: 1.85E+3nMAssay Description:Inhibitory concentration against aromatase protein from human placental microsomes using [1-beta-3H]-androstenedione; Competitive inhibitionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M66GDPubMed