Compile Data Set for Download or QSAR
Found 37 with Last Name = 'van den broeck' and Initial = 'w'
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50063995(Bedaquiline | CHEBI:72292 | TMC207)copy SMILEScopy InChI
Affinity DataIC50: 370nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452142(CHEMBL4212501)copy SMILEScopy InChI
Affinity DataIC50: 460nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452135(CHEMBL4213428)copy SMILEScopy InChI
Affinity DataIC50: 530nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452136(CHEMBL4206467)copy SMILEScopy InChI
Affinity DataIC50: 880nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452140(CHEMBL4204414)copy SMILEScopy InChI
Affinity DataIC50: 890nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50279196(CHEMBL4162672)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50063995(Bedaquiline | CHEBI:72292 | TMC207)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50279217(CHEMBL4177019)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Effective concentration on alkaline phosphatase activity in human T47D breast carcinoma cell line.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452143(CHEMBL4218132)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50279222(CHEMBL4176516)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50279216(CHEMBL4169823)copy SMILEScopy InChI
Affinity DataIC50: 3.50E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50279193(CHEMBL4169545)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452145(CHEMBL4206931)copy SMILEScopy InChI
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibition of CYP3A4 (unknown origin) after 20 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50279194(CHEMBL4166400)copy SMILEScopy InChI
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50279219(CHEMBL4159957)copy SMILEScopy InChI
Affinity DataIC50: 6.30E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50279197(CHEMBL4159307)copy SMILEScopy InChI
Affinity DataIC50: 6.90E+3nMAssay Description:Effective concentration on alkaline phosphatase activity in human T47D breast carcinoma cell line.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50279200(CHEMBL4162513)copy SMILEScopy InChI
Affinity DataIC50: 7.90E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452146(CHEMBL4216673)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin) after 20 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50279195(CHEMBL4170272)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50279192(CHEMBL4167910)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50279218(CHEMBL4159990)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Effective concentration against PR (progesterone receptor)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R0GPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452135(CHEMBL4213428)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin) after 20 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452143(CHEMBL4218132)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin) after 20 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452142(CHEMBL4212501)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin) after 20 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452140(CHEMBL4204414)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin) after 20 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452136(CHEMBL4206467)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin) after 20 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452134(CHEMBL4210920)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin) after 20 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50063995(Bedaquiline | CHEBI:72292 | TMC207)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin) after 20 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMedDrugBank
TargetCytochrome P450 3A4(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50452144(CHEMBL4205718)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin) after 20 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X3511SPubMed
TargetDNA polymerase beta(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50336503(10-acetyl-11-(3-(benzyloxy)-4-methoxyphenyl)-3,3-d...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human DNA polymerase betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M3732PubMed
TargetDNA polymerase alpha catalytic subunit(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50336502(10-acetyl-11-(2,4-dichlorophenyl)-3,3-dimethyl-2,3...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human DNA polymerase alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M3732PubMed
TargetDNA polymerase beta(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50336502(10-acetyl-11-(2,4-dichlorophenyl)-3,3-dimethyl-2,3...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human DNA polymerase betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M3732PubMed
TargetDNA polymerase subunit gamma-1(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50336503(10-acetyl-11-(3-(benzyloxy)-4-methoxyphenyl)-3,3-d...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human DNA polymerase gammaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M3732PubMed
TargetDNA polymerase alpha catalytic subunit(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50336503(10-acetyl-11-(3-(benzyloxy)-4-methoxyphenyl)-3,3-d...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human DNA polymerase alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M3732PubMed
TargetDNA polymerase subunit gamma-1(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50336502(10-acetyl-11-(2,4-dichlorophenyl)-3,3-dimethyl-2,3...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human DNA polymerase gammaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M3732PubMed
TargetTranslocator protein(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50336501(10-acetyl-11-(4-(benzyloxy)-2-chlorophenyl)-6-hydr...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+7nMAssay Description:Inhibition of peripheral benzodiazepine BZD receptor by radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M3732PubMed
TargetTranslocator protein(Homo sapiens (Human))
Tibotec BVBA

Curated by ChEMBL
LigandPNGBDBM50336501(10-acetyl-11-(4-(benzyloxy)-2-chlorophenyl)-6-hydr...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+7nMAssay Description:Inhibition of peripheral benzodiazepine BZD receptor by radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M3732PubMed