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Found 2534 with Last Name = 'barf' and Initial = 'ta'
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054764((E)-3-[3-(2-Dimethylamino-ethyl)-1H-indol-5-yl]-N-...)
Affinity DataKi:  0.200nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1D receptor beta expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054764((E)-3-[3-(2-Dimethylamino-ethyl)-1H-indol-5-yl]-N-...)
Affinity DataKi:  0.300nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1D receptor alpha expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054764((E)-3-[3-(2-Dimethylamino-ethyl)-1H-indol-5-yl]-N-...)
Affinity DataKi:  1.30nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1A receptor expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054762(CHEMBL143512 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  2.80nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1D receptor alpha expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054761(CHEMBL143767 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  3.20nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1D receptor alpha expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50005835((3-[2-(dimethylamino)ethyl]-1H-indol-5-yl)-N-methy...)
Affinity DataKi:  5.70nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1D receptor alpha expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054757(CHEMBL143510 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  12nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1D receptor alpha expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054762(CHEMBL143512 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  14nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1D receptor beta expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054762(CHEMBL143512 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  18nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1A receptor expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054762(CHEMBL143512 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  18nMAssay Description:Compound was tested for intrinsic efficacy against human 5-hydroxytryptamine 1D receptor beta measured as the reduction of forskolin-stimulated cAMP.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054762(CHEMBL143512 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  19nMAssay Description:Compound was tested for intrinsic efficacy against human 5-hydroxytryptamine 1D receptor alpha measured as the reduction of forskolin-stimulated cAMP...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50005835((3-[2-(dimethylamino)ethyl]-1H-indol-5-yl)-N-methy...)
Affinity DataKi:  22nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1D receptor beta expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054760(CHEMBL143967 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  23nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1A receptor expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50005835((3-[2-(dimethylamino)ethyl]-1H-indol-5-yl)-N-methy...)
Affinity DataKi:  24nMAssay Description:Compound was tested for intrinsic efficacy against human 5-hydroxytryptamine 1D receptor beta measured as the reduction of forskolin-stimulated cAMP.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054757(CHEMBL143510 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  27nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1A receptor expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054761(CHEMBL143767 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  28nMAssay Description:Compound was tested for intrinsic efficacy against human 5-hydroxytryptamine 1D receptor beta measured as the reduction of forskolin-stimulated cAMP.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054757(CHEMBL143510 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  29nMAssay Description:Compound was tested for intrinsic efficacy against human 5-hydroxytryptamine 1D receptor beta measured as the reduction of forskolin-stimulated cAMP.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054761(CHEMBL143767 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  30nMAssay Description:Compound was tested for intrinsic efficacy against human 5-hydroxytryptamine 1D receptor alpha measured as the reduction of forskolin-stimulated cAMP...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50005835((3-[2-(dimethylamino)ethyl]-1H-indol-5-yl)-N-methy...)
Affinity DataKi:  30nMAssay Description:Compound was tested for intrinsic efficacy against human 5-hydroxytryptamine 1D receptor alpha measured as the reduction of forskolin-stimulated cAMP...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054761(CHEMBL143767 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  32nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1D receptor beta expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054760(CHEMBL143967 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  36nMAssay Description:Compound was tested for intrinsic efficacy against human 5-hydroxytryptamine 1D receptor alpha measured as the reduction of forskolin-stimulated cAMP...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054757(CHEMBL143510 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  37nMAssay Description:Compound was tested for intrinsic efficacy against human 5-hydroxytryptamine 1D receptor beta measured as the reduction of forskolin-stimulated cAMP.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054761(CHEMBL143767 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  40nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1A receptor expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054760(CHEMBL143967 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  88nMAssay Description:Compound was tested for intrinsic efficacy against human 5-hydroxytryptamine 1D receptor beta measured as the reduction of forskolin-stimulated cAMP.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054764((E)-3-[3-(2-Dimethylamino-ethyl)-1H-indol-5-yl]-N-...)
Affinity DataKi:  104nMAssay Description:Compound was tested for intrinsic efficacy against human 5-hydroxytryptamine 1D receptor beta measured as the reduction of forskolin-stimulated cAMP.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054757(CHEMBL143510 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  171nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1D receptor alpha expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054760(CHEMBL143967 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  190nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1D receptor alpha expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50005835((3-[2-(dimethylamino)ethyl]-1H-indol-5-yl)-N-methy...)
Affinity DataKi: >218nMAssay Description:Compound was tested for binding affinity against cloned human dopamine D2 receptor expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054760(CHEMBL143967 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  246nMAssay Description:Compound was tested for binding affinity against cloned human 5-HT1D beta receptor expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50005835((3-[2-(dimethylamino)ethyl]-1H-indol-5-yl)-N-methy...)
Affinity DataKi:  341nMAssay Description:Compound was tested for binding affinity against cloned human 5-hydroxytryptamine 1A receptor expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054760(CHEMBL143967 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  502nMAssay Description:Compound was tested for binding affinity against cloned human dopamine D2 receptor expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054761(CHEMBL143767 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  538nMAssay Description:Compound was tested for binding affinity against cloned human dopamine D2 receptor expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054757(CHEMBL143510 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  637nMAssay Description:Compound was tested for binding affinity against cloned human dopamine D2 receptor expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054762(CHEMBL143512 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataKi:  658nMAssay Description:Compound was tested for binding affinity against cloned human dopamine D2 receptor expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054764((E)-3-[3-(2-Dimethylamino-ethyl)-1H-indol-5-yl]-N-...)
Affinity DataKi: >1.00E+3nMAssay Description:Compound was tested for binding affinity against cloned human Dopamine receptor D2 expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of Groningen

Curated by ChEMBL
LigandPNGBDBM50054761(CHEMBL143767 | Trifluoro-methanesulfonic acid 3-(2...)
Affinity DataIC50:  8.40nMAssay Description:Compound was tested for binding affinity against human 5-hydroxytryptamine 1D receptor alpha clones expressed in human embryonic kidney (HEK 293) cel...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267888(4-{8-amino-3-[(2R)-4-(3-ethoxypropanoyl)morpholin-...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267889(4-{8-amino-5-chloro-3-[(2R)-morpholin-2-yl]imidazo...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267891(4-(8-amino-5-methyl-3-{(2R)-4-[(3-methyloxetan-3-y...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267892(4-(8-amino-3-{(2R)-4-[(3-methyloxetan-3-yl)methyl]...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267893(4-{8-amino-3-[(2R)-4-(cyclopropylmethyl)morpholin-...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267894(4-(8-amino-5-methyl-3-{(2R)-4-[(1-methyl-1H-pyrazo...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267895(4-{8-amino-3-[(2R)-4-(3-methoxypropanoyl)morpholin...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267896(4-{8-amino-3-[(2R)-4-ethylmorpholin-2-yl]-5-methyl...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267897(4-{8-amino-3-[(2R)-4-(cyclopropylcarbonyl)morpholi...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267898(4-(8-amino-3-{(2R)-4-[(3-methyloxetan-3-yl)carbony...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267899(4-(8-amino-5-methyl-3-{(2R)-4-[(3-methyloxetan-3-y...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267900(4-(8-amino-3-{(2R,5S)-5-methyl-4-[(3-methyloxetan-...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267901(4-{8-amino-3-[(2R,5S)-4-(cyclopropylcarbonyl)-5-me...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Merck Sharp & Dohme

US Patent
LigandPNGBDBM267902(4-{8-amino-3-[(2R)-4-(hydroxyacetyl)morpholin-2-yl...)
Affinity DataIC50: <10nMAssay Description:BTK enzymatic activity was determined with the LANCE (Lanthanide Chelate Excite) TR-FRET (Time-resolved fluorescence resonance energy transfer) assay...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
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