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Found 71 with Last Name = 'enomoto' and Initial = 't'
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50044633(CHEMBL3310801)
Affinity DataIC50:  190nMAssay Description:Inhibition of human ERG channelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50044630(CHEMBL3310798)
Affinity DataIC50:  230nMAssay Description:Inhibition of human ERG channelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50044632(CHEMBL3310800)
Affinity DataIC50:  300nMAssay Description:Inhibition of human ERG channelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50492651(CHEMBL2407175)
Affinity DataIC50:  670nMAssay Description:Inhibition of human ERG by automated planar patch-clamp systemMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50428141(CHEMBL2336055)
Affinity DataIC50:  800nMAssay Description:Inhibition of human ERG assessed as decrease in tail current amplitude measured after 5 mins by whole cell patch clamp techniqueMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50492655(CHEMBL2407171)
Affinity DataIC50:  920nMAssay Description:Inhibition of human ERG by automated planar patch-clamp systemMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50492654(CHEMBL2407170)
Affinity DataIC50:  1.48E+3nMAssay Description:Inhibition of human ERG by automated planar patch-clamp systemMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50019335(CHEMBL3289440)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibition of human ERG channelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50019335(CHEMBL3289440)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibition of human ERG tail current after 5 mins by patch-clamp methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Sumitomo Dainippon Pharma

Curated by ChEMBL
LigandPNGBDBM50130927(CHEMBL3633184)
Affinity DataIC50: >2.00E+3nMAssay Description:Inhibition of CYP2D6 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
Sumitomo Dainippon Pharma

Curated by ChEMBL
LigandPNGBDBM50130927(CHEMBL3633184)
Affinity DataIC50: >2.00E+3nMAssay Description:Inhibition of CYP2C19 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Sumitomo Dainippon Pharma

Curated by ChEMBL
LigandPNGBDBM50130927(CHEMBL3633184)
Affinity DataIC50: >2.00E+3nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Sumitomo Dainippon Pharma

Curated by ChEMBL
LigandPNGBDBM50130927(CHEMBL3633184)
Affinity DataIC50: >2.00E+3nMAssay Description:Inhibition of CYP1A2 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Sumitomo Dainippon Pharma

Curated by ChEMBL
LigandPNGBDBM50130927(CHEMBL3633184)
Affinity DataIC50: >2.00E+3nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50428138(CHEMBL2336059)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of human ERG assessed as decrease in tail current amplitude measured after 5 mins by whole cell patch clamp techniqueMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50044631(CHEMBL3310799)
Affinity DataIC50:  2.54E+3nMAssay Description:Inhibition of human ERG channelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50492653(CHEMBL2407173)
Affinity DataIC50:  2.54E+3nMAssay Description:Inhibition of human ERG by automated planar patch-clamp systemMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50019334(CHEMBL3289444)
Affinity DataIC50:  2.75E+3nMAssay Description:Inhibition of human ERG tail current after 5 mins by patch-clamp methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50492652(CHEMBL2407172)
Affinity DataIC50:  2.80E+3nMAssay Description:Inhibition of human ERG by automated planar patch-clamp systemMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50044629(CHEMBL2407174)
Affinity DataIC50:  2.89E+3nMAssay Description:Inhibition of human ERG channelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50044629(CHEMBL2407174)
Affinity DataIC50:  2.89E+3nMAssay Description:Inhibition of human ERG by automated planar patch-clamp systemMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50428140(CHEMBL2336056)
Affinity DataIC50:  3.50E+3nMAssay Description:Inhibition of human ERG assessed as decrease in tail current amplitude measured after 5 mins by whole cell patch clamp techniqueMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50019336(CHEMBL3289442)
Affinity DataIC50:  3.63E+3nMAssay Description:Inhibition of human ERG tail current after 5 mins by patch-clamp methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50428139(CHEMBL2336057)
Affinity DataIC50:  3.90E+3nMAssay Description:Inhibition of human ERG assessed as decrease in tail current amplitude measured after 5 mins by whole cell patch clamp techniqueMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50044634(CHEMBL3310802)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human ERG channelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50019337(CHEMBL3289443)
Affinity DataIC50:  1.70E+4nMAssay Description:Inhibition of human ERG tail current after 5 mins by patch-clamp methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50172721(CHEMBL3814026)
Affinity DataEC50:  860nMAssay Description:Agonist activity at GAL4 fused LXRalpha (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50173929(CHEMBL3814025)
Affinity DataEC50:  1.96E+3nMAssay Description:Agonist activity at GAL4 fused LXRalpha (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50174995(CHEMBL3814000)
Affinity DataEC50:  2.89E+3nMAssay Description:Agonist activity at GAL4 fused LXRalpha (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50176997(CHEMBL3814071)
Affinity DataEC50:  3.14E+3nMAssay Description:Agonist activity at GAL4 fused LXRalpha (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50179403(CHEMBL3814381)
Affinity DataEC50:  360nMAssay Description:Agonist activity at GAL4 fused LXRalpha (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50179430(CHEMBL3813703)
Affinity DataEC50:  400nMAssay Description:Agonist activity at GAL4 fused LXRalpha (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50179431(CHEMBL3814351)
Affinity DataEC50:  3.74E+3nMAssay Description:Agonist activity at GAL4 fused LXRalpha (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50179484(CHEMBL3814980)
Affinity DataEC50:  340nMAssay Description:Agonist activity at GAL4 fused LXRalpha (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50179485(CHEMBL3814799)
Affinity DataEC50:  330nMAssay Description:Agonist activity at GAL4 fused LXRalpha (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50179485(CHEMBL3814799)
Affinity DataEC50:  330nMAssay Description:Agonist activity at GAL4 fused LXRalpha (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM19993(CHEMBL62136 | N-[4-(1,1,1,3,3,3-hexafluoro-2-hydro...)
Affinity DataEC50:  490nMAssay Description:Agonist activity at GAL4 fused LXRalpha (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50064330(CHEMBL3403710)
Affinity DataEC50:  1.40E+3nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50094851(CHEMBL3589803)
Affinity DataEC50:  1.15E+3nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50172720(CHEMBL3814017)
Affinity DataEC50:  800nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50172721(CHEMBL3814026)
Affinity DataEC50:  610nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50173929(CHEMBL3814025)
Affinity DataEC50:  500nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50179486(CHEMBL3814224)
Affinity DataEC50:  1.81E+3nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50174995(CHEMBL3814000)
Affinity DataEC50:  2.85E+3nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50179488(CHEMBL3814807)
Affinity DataEC50:  1.88E+3nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50176997(CHEMBL3814071)
Affinity DataEC50:  700nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50179489(CHEMBL3814297)
Affinity DataEC50:  1.66E+3nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50179490(CHEMBL3813961)
Affinity DataEC50:  2.87E+3nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50179491(CHEMBL3814806)
Affinity DataEC50:  2.33E+3nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Kowa

Curated by ChEMBL
LigandPNGBDBM50179403(CHEMBL3814381)
Affinity DataEC50:  120nMAssay Description:Agonist activity at GAL4 fused LXRbeta-LBD (unknown origin) transfected in CHOK1 cells after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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