Compile Data Set for Download or QSAR
Found 116 with Last Name = 'chander' and Initial = 'sk'
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307918(2-(5-((1H-1,2,4-triazol-1-yl)methyl)-3'-chloro-4'-...)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307901(5-((1H-1,2,4-triazol-1-yl)methyl)-3'-chloro-4'-hyd...)copy SMILEScopy InChI
Affinity DataIC50: 0.150nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24341(4-{[(4-chloro-3-hydroxyphenyl)methyl](4H-1,2,4-tri...)copy SMILEScopy InChI
Affinity DataIC50: 0.180nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307900(5-((1H-1,2,4-triazol-1-yl)methyl)-4'-hydroxybiphen...)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307899(5-((1H-1,2,4-triazol-1-yl)methyl)biphenyl-2-carbon...)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307919(5-((1H-1,2,4-triazol-1-yl)methyl)-3'-chlorobipheny...)copy SMILEScopy InChI
Affinity DataIC50: 0.220nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307902(5-((1H-1,2,4-triazol-1-yl)methyl)-4'-chloro-3'-hyd...)copy SMILEScopy InChI
Affinity DataIC50: 0.220nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307881(3'-((1H-1,2,4-triazol-1-yl)methyl)-3-chloro-5'-(2-...)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24328(4-{[(4-hydroxy-3-iodophenyl)methyl](4H-1,2,4-triaz...)copy SMILEScopy InChI
Affinity DataIC50: 0.330nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307882(5'-((1H-1,2,4-triazol-1-yl)methyl)-4-chloro-2'-cya...)copy SMILEScopy InChI
Affinity DataIC50: 0.350nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24344(4-({[3-hydroxy-4-(trifluoromethyl)phenyl]methyl}(4...)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307884(3-CHLORO-2'-CYANO-5'-(1H-1,2,4-TRIAZOL-1-YLMETHYL)...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307883(5'-((1H-1,2,4-triazol-1-yl)methyl)-2'-cyanobipheny...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307916(2-(5-((1H-1,2,4-triazol-1-yl)methyl)biphenyl-3-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24342(4-{[(4-bromo-3-hydroxyphenyl)methyl](4H-1,2,4-tria...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM10016(4-{[(4-bromophenyl)methyl](4H-1,2,4-triazol-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HT2MHGPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM10016(4-{[(4-bromophenyl)methyl](4H-1,2,4-triazol-4-yl)a...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24332(4-{[(3-chloro-4-hydroxy-5-methoxyphenyl)methyl](4H...)copy SMILEScopy InChI
Affinity DataIC50: 0.510nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24340(4-{[(4-fluoro-3-hydroxyphenyl)methyl](4H-1,2,4-tri...)copy SMILEScopy InChI
Affinity DataIC50: 0.600nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24335((5-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]m...)copy SMILEScopy InChI
Affinity DataIC50: 0.770nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307915(6-((1H-1,2,4-triazol-1-yl)methyl)-3'-chloro-4'-hyd...)copy SMILEScopy InChI
Affinity DataIC50: 0.800nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM10020((2-bromo-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 0.820nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HT2MHGPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM10020((2-bromo-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 0.820nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24331(4-({[4-hydroxy-3-(trifluoromethyl)phenyl]methyl}(4...)copy SMILEScopy InChI
Affinity DataIC50: 0.880nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM13061(4,4 -(1H-1,2,4-triazol-1-ylmethanediyl)dibenzonitr...)copy SMILEScopy InChI
Affinity DataIC50: 0.890nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMedDrugBank
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24336((2-chloro-5-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-y...)copy SMILEScopy InChI
Affinity DataIC50: 0.920nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24327(4-{[(3-bromo-4-hydroxyphenyl)methyl](4H-1,2,4-tria...)copy SMILEScopy InChI
Affinity DataIC50: 1.10nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24343(4-{[(3-hydroxy-4-methoxyphenyl)methyl](4H-1,2,4-tr...)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University of Bath

LigandPNGBDBM13058(6-oxo-6,7,8,9,10,11-hexahydrocyclohepta[c]chromen-...)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:The extent of in vitro inhibition of sulfatase activities was assessed using intact monolayers of JEG-3 cells. Sulfatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24320((4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]m...)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University of Bath

LigandPNGBDBM13058(6-oxo-6,7,8,9,10,11-hexahydrocyclohepta[c]chromen-...)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:Inhibition of steroid sulfatase in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM10015(2-[3-(1-cyano-1-methylethyl)-5-(1H-1,2,4-triazol-1...)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMedDrugBank
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307914(6-((1H-1,2,4-triazol-1-yl)methyl)biphenyl-3-carbon...)copy SMILEScopy InChI
Affinity DataIC50: 1.70nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307885(2'-((1H-1,2,4-triazol-1-yl)methyl)-3-chloro-5'-cya...)copy SMILEScopy InChI
Affinity DataIC50: 1.90nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307886(5'-((1H-1,2,4-triazol-1-yl)methyl)-2'-cyanobipheny...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM10019((2-chloro-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-y...)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM10019((2-chloro-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-y...)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HT2MHGPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307887(5'-((1H-1,2,4-triazol-1-yl)methyl)-3-chloro-2'-cya...)copy SMILEScopy InChI
Affinity DataIC50: 2.40nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24326(4-{[(3-chloro-4-hydroxyphenyl)methyl](4H-1,2,4-tri...)copy SMILEScopy InChI
Affinity DataIC50: 2.5nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24339(4-{[(3-hydroxyphenyl)methyl](4H-1,2,4-triazol-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 2.80nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24329(4-{[(4-hydroxy-3-methoxyphenyl)methyl](4H-1,2,4-tr...)copy SMILEScopy InChI
Affinity DataIC50: 2.80nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24323((2-chloro-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-y...)copy SMILEScopy InChI
Affinity DataIC50: 2.90nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24325(4-{[(3-fluoro-4-hydroxyphenyl)methyl](4H-1,2,4-tri...)copy SMILEScopy InChI
Affinity DataIC50: 2.90nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24337((2-bromo-5-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl...)copy SMILEScopy InChI
Affinity DataIC50: 3.90nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307911(4-((1H-1,2,4-triazol-1-yl)methyl)biphenyl-2-carbon...)copy SMILEScopy InChI
Affinity DataIC50: 4.60nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University of Bath

LigandPNGBDBM50307884(3-CHLORO-2'-CYANO-5'-(1H-1,2,4-TRIAZOL-1-YLMETHYL)...)copy SMILEScopy InChI
Affinity DataIC50: 5.5nMAssay Description:Inhibition of steroid sulfatase in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM50307917(2-(5-((1H-1,2,4-triazol-1-yl)methyl)-4'-hydroxybip...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of aromatse in human JEG3 cells by scintillation spectrometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959JGFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24333(4-{[(3,5-dichloro-4-hydroxyphenyl)methyl](4H-1,2,4...)copy SMILEScopy InChI
Affinity DataIC50: 7.60nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM10018((4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]m...)copy SMILEScopy InChI
Affinity DataIC50: 12nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HT2MHGPubMed
TargetAromatase(Homo sapiens (Human))
University of Bath

Curated by ChEMBL
LigandPNGBDBM24338((5-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]m...)copy SMILEScopy InChI
Affinity DataIC50: 12nMpH: 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348HP4PubMed
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