Compile Data Set for Download or QSAR
Found 170 with Last Name = 'kurasaki' and Initial = 'h'
TargetMu-type opioid receptor(Homo sapiens (Human))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313166((S)-(2-hydroxy-6-methylphenyl)(2,3,5,7a-tetrahydro...)copy SMILEScopy InChI
Affinity DataKi:  3.20E+3nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313167((S,E)-(2,3,5,6,7,9a-hexahydro-1H-pyrrolo[1,2-a]aze...)copy SMILEScopy InChI
Affinity DataKi:  4.00E+3nMAssay Description:Displacement of [3H]U69593 from rat kappa opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50211219(elaeocarpenine)copy SMILEScopy InChI
Affinity DataKi:  1.20E+4nMAssay Description:Displacement of [3H]U69593 from rat kappa opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313167((S,E)-(2,3,5,6,7,9a-hexahydro-1H-pyrrolo[1,2-a]aze...)copy SMILEScopy InChI
Affinity DataKi:  1.30E+4nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50211219(elaeocarpenine)copy SMILEScopy InChI
Affinity DataKi:  1.40E+4nMAssay Description:Displacement of [3H]DADLE from human delta opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50211219(elaeocarpenine)copy SMILEScopy InChI
Affinity DataKi:  1.80E+4nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313164((S)-(1,2,3,5,6,8a-hexahydroindolizin-8-yl)(2-metho...)copy SMILEScopy InChI
Affinity DataKi:  2.00E+4nMAssay Description:Displacement of [3H]U69593 from rat kappa opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313163((S)-(1,2,3,5,6,8a-hexahydroindolizin-8-yl)(2-hydro...)copy SMILEScopy InChI
Affinity DataKi:  2.40E+4nMAssay Description:Displacement of [3H]U69593 from rat kappa opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313166((S)-(2-hydroxy-6-methylphenyl)(2,3,5,7a-tetrahydro...)copy SMILEScopy InChI
Affinity DataKi:  3.50E+4nMAssay Description:Displacement of [3H]U69593 from rat kappa opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313163((S)-(1,2,3,5,6,8a-hexahydroindolizin-8-yl)(2-hydro...)copy SMILEScopy InChI
Affinity DataKi:  4.50E+4nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313165((S)-(1,2,3,5,6,8a-hexahydroindolizin-8-yl)(2-hydro...)copy SMILEScopy InChI
Affinity DataKi:  4.90E+4nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313165((S)-(1,2,3,5,6,8a-hexahydroindolizin-8-yl)(2-hydro...)copy SMILEScopy InChI
Affinity DataKi:  8.30E+4nMAssay Description:Displacement of [3H]U69593 from rat kappa opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313163((S)-(1,2,3,5,6,8a-hexahydroindolizin-8-yl)(2-hydro...)copy SMILEScopy InChI
Affinity DataKi:  9.40E+4nMAssay Description:Displacement of [3H]DADLE from human delta opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313164((S)-(1,2,3,5,6,8a-hexahydroindolizin-8-yl)(2-metho...)copy SMILEScopy InChI
Affinity DataKi: >2.00E+5nMAssay Description:Displacement of [3H]DAMGO from human mu opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313164((S)-(1,2,3,5,6,8a-hexahydroindolizin-8-yl)(2-metho...)copy SMILEScopy InChI
Affinity DataKi: >2.00E+5nMAssay Description:Displacement of [3H]DADLE from human delta opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313166((S)-(2-hydroxy-6-methylphenyl)(2,3,5,7a-tetrahydro...)copy SMILEScopy InChI
Affinity DataKi: >2.00E+5nMAssay Description:Displacement of [3H]DADLE from human delta opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313165((S)-(1,2,3,5,6,8a-hexahydroindolizin-8-yl)(2-hydro...)copy SMILEScopy InChI
Affinity DataKi: >2.00E+5nMAssay Description:Displacement of [3H]DADLE from human delta opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Kyorin Pharmaceutical Co., Ltd

Curated by ChEMBL
LigandPNGBDBM50313167((S,E)-(2,3,5,6,7,9a-hexahydro-1H-pyrrolo[1,2-a]aze...)copy SMILEScopy InChI
Affinity DataKi: >2.00E+5nMAssay Description:Displacement of [3H]DADLE from human delta opioid receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35TRMPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082445(CHEMBL3422978)copy SMILEScopy InChI
Affinity DataIC50: 0.390nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082380(CHEMBL3422952)copy SMILEScopy InChI
Affinity DataIC50: 0.730nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082429(CHEMBL3422970)copy SMILEScopy InChI
Affinity DataIC50: 0.870nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082385(CHEMBL3422959)copy SMILEScopy InChI
Affinity DataIC50: 0.890nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082440(CHEMBL3422977)copy SMILEScopy InChI
Affinity DataIC50: 0.990nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082382(CHEMBL3422954)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082435(CHEMBL3422976)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082390(CHEMBL3422964)copy SMILEScopy InChI
Affinity DataIC50: 1.40nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082394(CHEMBL3422966)copy SMILEScopy InChI
Affinity DataIC50: 1.60nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082388(CHEMBL3422962)copy SMILEScopy InChI
Affinity DataIC50: 1.70nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082383(CHEMBL3422957)copy SMILEScopy InChI
Affinity DataIC50: 1.70nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082427(CHEMBL3422968)copy SMILEScopy InChI
Affinity DataIC50: 1.80nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082430(CHEMBL3422971)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082432(CHEMBL3422973)copy SMILEScopy InChI
Affinity DataIC50: 2.10nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082520(CHEMBL3422983)copy SMILEScopy InChI
Affinity DataIC50: 2.10nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082520(CHEMBL3422983)copy SMILEScopy InChI
Affinity DataIC50: 2.13nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082434(CHEMBL3422975)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082391(CHEMBL3422965)copy SMILEScopy InChI
Affinity DataIC50: 2.5nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082381(CHEMBL3422953)copy SMILEScopy InChI
Affinity DataIC50: 2.90nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Escherichia coli)
Kyorin Pharmaceutical Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50200120(CHEMBL260091 | CHIR-090 | US10875832, Compound ChI...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of Escherichia coli LpxC using UDP-3-O-(R-3-hydroxymyristoyl)GlcNAc as substrate after 60 mins by OPA reagent based fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC9313PubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Escherichia coli)
Kyorin Pharmaceutical Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50200120(CHEMBL260091 | CHIR-090 | US10875832, Compound ChI...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of Escherichia coli LpxC using UDP-3-O-(R-3-hydroxymyristoyl)GlcNAc as substrate measured after 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DV1NWVPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082376(CHEMBL3422948)copy SMILEScopy InChI
Affinity DataIC50: 3.20nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082387(CHEMBL3422961)copy SMILEScopy InChI
Affinity DataIC50: 3.30nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082340(CHEMBL3422947)copy SMILEScopy InChI
Affinity DataIC50: 3.90nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082389(CHEMBL3422963)copy SMILEScopy InChI
Affinity DataIC50: 4.20nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082428(CHEMBL3422969)copy SMILEScopy InChI
Affinity DataIC50: 4.20nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082332(CHEMBL3422765)copy SMILEScopy InChI
Affinity DataIC50: 4.80nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082517(CHEMBL3422980)copy SMILEScopy InChI
Affinity DataIC50: 4.90nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082409(CHEMBL3422967)copy SMILEScopy InChI
Affinity DataIC50: 5.20nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Escherichia coli)
Kyorin Pharmaceutical Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50501133(CHEMBL3827314)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of Escherichia coli LpxC using UDP-3-O-(R-3-hydroxymyristoyl)GlcNAc as substrate measured after 60 mins by fluorescence analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DV1NWVPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082433(CHEMBL3422974)copy SMILEScopy InChI
Affinity DataIC50: 6.70nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50082519(CHEMBL3422982)copy SMILEScopy InChI
Affinity DataIC50: 7.90nMAssay Description:Inhibition of MK499 binding to human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN75MCPubMed
Displayed 1 to 50 (of 170 total ) | Next | Last >>
Jump to: