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TargetCarboxylic ester hydrolase(Equus caballus (Horse))
National Chung-Hsing University

Curated by ChEMBL
LigandPNGBDBM50135653(2,4,6,8,10,12-hexa(2-chloro phenylmethyl)-2,4,6,8,...)
Affinity DataKi:  10nMAssay Description:Inhibitory activity of the compound against ButyrylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50192958(CHEMBL385894 | N-[6-(3-adamantyl-ureido)-hexanoyl]...)
Affinity DataKi:  15nMAssay Description:Inhibition of human recombinant soluble Epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
National Chung-Hsing University

Curated by ChEMBL
LigandPNGBDBM50135653(2,4,6,8,10,12-hexa(2-chloro phenylmethyl)-2,4,6,8,...)
Affinity DataKi:  39nMAssay Description:Inhibitory activity of the compound against acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
National Chung-Hsing University

Curated by ChEMBL
LigandPNGBDBM50135654(2,4,6,8,10,12-hexa(3,5-dimethoxyphenylmethyl)-2,4,...)
Affinity DataKi:  60nMAssay Description:Inhibitory activity of the compound against ButyrylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
National Chung-Hsing University

Curated by ChEMBL
LigandPNGBDBM50135654(2,4,6,8,10,12-hexa(3,5-dimethoxyphenylmethyl)-2,4,...)
Affinity DataKi:  130nMAssay Description:Inhibitory activity of the compound against acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
National Chung-Hsing University

Curated by ChEMBL
LigandPNGBDBM50135652(2,6,8N,9,11,12-hexabenzo[d][1,3]dioxol-5-ylmethyl-...)
Affinity DataKi:  310nMAssay Description:Inhibitory activity of the compound against ButyrylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
National Chung-Hsing University

Curated by ChEMBL
LigandPNGBDBM50135652(2,6,8N,9,11,12-hexabenzo[d][1,3]dioxol-5-ylmethyl-...)
Affinity DataKi:  320nMAssay Description:Inhibitory activity of the compound against acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
National Chung-Hsing University

Curated by ChEMBL
LigandPNGBDBM50135655(2,4,6,8,10,12-Hexabenzyl-2,4,6,8,10,12-hexaazatetr...)
Affinity DataKi:  900nMAssay Description:Inhibitory activity of the compound against ButyrylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
National Chung-Hsing University

Curated by ChEMBL
LigandPNGBDBM50135655(2,4,6,8,10,12-Hexabenzyl-2,4,6,8,10,12-hexaazatetr...)
Affinity DataKi:  4.00E+3nMAssay Description:Inhibitory activity of the compound against acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMast/stem cell growth factor receptor Kit(Homo sapiens (Human))
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50521626(CHEMBL4448433)
Affinity DataIC50:  0.0200nMAssay Description:Inhibition of human c-KIT A loop exon 17 D820Y single mutant using poly (Glu,Tyr) 4:1 as substrate in presence of 33P-gamma-ATP by hotspot kinase ass...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50519725(CHEMBL4513768)
Affinity DataIC50:  0.100nMAssay Description:Inhibition of wild type FLT3 (unknown origin) expressed in HEK293T cells assessed as decrease in FLT3 phosphorylation at 0.1 to 1000 nM after 1 hr by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50519725(CHEMBL4513768)
Affinity DataIC50:  0.100nMAssay Description:Inhibition of wild type FLT3 D835Y mutant (unknown origin) expressed in HEK293T cells assessed as decrease in FLT3 D835Y phosphorylation at 0.1 to 10...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50519725(CHEMBL4513768)
Affinity DataIC50:  0.100nMAssay Description:Inhibition of wild type FLT3 ITD mutant (unknown origin) expressed in HEK293T cells assessed as decrease in FLT3 ITD phosphorylation at 0.1 to 1000 n...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetMast/stem cell growth factor receptor Kit(Homo sapiens (Human))
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50521626(CHEMBL4448433)
Affinity DataIC50:  0.120nMAssay Description:Inhibition of human c-KIT A loop exon 17 Y823D single mutant using poly (Glu,Tyr) 4:1 as substrate in presence of 33P-gamma-ATP by hotspot kinase ass...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMast/stem cell growth factor receptor Kit(Homo sapiens (Human))
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50521626(CHEMBL4448433)
Affinity DataIC50:  0.180nMAssay Description:Inhibition of human c-KIT A loop exon 11/17 V560G/N822K double mutant using poly (Glu,Tyr) 4:1 as substrate in presence of 33P-gamma-ATP by hotspot k...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217458(CHEMBL244192 | cis-1-adamantan-1-yl-3-[4-(4-methox...)
Affinity DataIC50:  0.550nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217444(CHEMBL244002 | cis-4-{4-[3-(4-trifluoromethoxyphen...)
Affinity DataIC50:  0.600nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217457(CHEMBL397694 | trans-1-adamantan-1-yl-3-[4-(4-nitr...)
Affinity DataIC50:  0.640nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMast/stem cell growth factor receptor Kit(Homo sapiens (Human))
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50521626(CHEMBL4448433)
Affinity DataIC50:  0.670nMAssay Description:Inhibition of human c-KIT A loop exon 17 D816H single mutant using poly (Glu,Tyr) 4:1 as substrate in presence of 33P-gamma-ATP by hotspot kinase ass...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50196664(12-(3-adamantan-1-yl-ureido)-dodecanoic acid sec-b...)
Affinity DataIC50:  0.700nMAssay Description:Inhibition of human soluble epoxide hydrolase by fluorescent based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217469(CHEMBL244193 | cis-1-adamantan-1-yl-3-[4-(4-nitrop...)
Affinity DataIC50:  0.720nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217459(CHEMBL243335 | trans-1-adamantan-1-yl-3-[4-(4-fluo...)
Affinity DataIC50:  0.800nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50196661(12-(3-adamantan-1-yl-ureido)-dodecanoic acid butyl...)
Affinity DataIC50:  0.800nMAssay Description:Inhibition of human soluble epoxide hydrolase by fluorescent based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMast/stem cell growth factor receptor Kit(Homo sapiens (Human))
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50521626(CHEMBL4448433)
Affinity DataIC50:  0.810nMAssay Description:Inhibition of human c-KIT A loop exon 17 D820E single mutant using poly (Glu,Tyr) 4:1 as substrate in presence of 33P-gamma-ATP by hotspot kinase ass...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217446(CHEMBL396546 | cis-1-adamantan-1-yl-3-[4-(3,5-difl...)
Affinity DataIC50:  0.820nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217451(CHEMBL427695 | trans-1-adamantan-1-yl-3-[4-(4-meth...)
Affinity DataIC50:  0.870nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMast/stem cell growth factor receptor Kit(Homo sapiens (Human))
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50521626(CHEMBL4448433)
Affinity DataIC50:  0.890nMAssay Description:Inhibition of human c-KIT A loop exon 18 A829P single mutant using poly (Glu,Tyr) 4:1 as substrate in presence of 33P-gamma-ATP by hotspot kinase ass...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217439(CHEMBL244405 | cis-4-[4-(3-adamantan-1-ylureido)cy...)
Affinity DataIC50:  0.890nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50194498(1-[4-(4-fluoro-phenoxy)-cyclohexyl]-3-(4-trifluoro...)
Affinity DataIC50:  0.900nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217477(CHEMBL243793 | trans-4-{4-[3-(4-trifluoromethoxyph...)
Affinity DataIC50:  0.900nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217461(CHEMBL242898 | cis-1-adamantan-1-yl-3-(4-benzyloxy...)
Affinity DataIC50:  0.900nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMast/stem cell growth factor receptor Kit(Homo sapiens (Human))
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50521626(CHEMBL4448433)
Affinity DataIC50:  0.980nMAssay Description:Inhibition of human c-KIT JM domain exon 11 V560G single mutant using poly (Glu,Tyr) 4:1 as substrate in presence of 33P-gamma-ATP by hotspot kinase ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217473(CHEMBL243336 | trans-1-adamantan-1-yl-3-[4-(3,5-di...)
Affinity DataIC50:  1nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50196655(12-(3-adamantan-1-yl-ureido)-dodecanoic acid allyl...)
Affinity DataIC50:  1nMAssay Description:Inhibition of human soluble epoxide hydrolase by fluorescent based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50194500(1-adamantan-1-yl-3-[4-(4-fluoro-phenoxy)-cyclohexy...)
Affinity DataIC50:  1nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50196654(12-(3-adamantan-1-yl-ureido)-dodecanoic acid propy...)
Affinity DataIC50:  1nMAssay Description:Inhibition of human soluble epoxide hydrolase by fluorescent based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217454(CHEMBL395738 | cis-1-adamantan-1-yl-3-[4-(2,6-difl...)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50223391(1-Adamantan-1-yl-3-{3-[2-(2-ethoxy-ethoxy)-ethoxy]...)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolase by fluorescent based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50191859(1-adamantan-1-yl-3-[1-(2,2,2-trifluoro-acetyl)-pip...)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of soluble epoxide hydroxylase by kinetic fluorescent assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50196649(12-(3-adamantan-1-yl-ureido)-dodecanoic acid isopr...)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of human soluble epoxide hydrolase by fluorescent based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50223398(1-Adamantan-1-yl-3-{4-[2-(2-ethoxy-ethoxy)-ethoxy]...)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of human soluble epoxide hydrolase by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50191898(3-[4-(3-adamantan-1-yl-ureido)-piperidine-1-carbon...)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of soluble epoxide hydroxylase by kinetic fluorescent assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50191882(4-[4-(3-adamantan-1-yl-ureido)-piperidine-1-carbon...)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of soluble epoxide hydroxylase by kinetic fluorescent assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50223384(1-adamantan-1-yl-3-(4-pentyloxycylclohexyl)urea | ...)
Affinity DataIC50:  1.20nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolase by fluorescent based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50191867(1-adamantan-1-yl-3-[1-(pyridine-2-carbonyl)-piperi...)
Affinity DataIC50:  1.20nMAssay Description:Inhibition of soluble epoxide hydroxylase by kinetic fluorescent assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50196660(12-(3-adamantan-1-yl-ureido)-dodecanoic acid isobu...)
Affinity DataIC50:  1.20nMAssay Description:Inhibition of human soluble epoxide hydrolase by fluorescent based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50223389(1-Adamantan-1-yl-3-[4-(3-morpholin-4-yl-propoxy)-p...)
Affinity DataIC50:  1.30nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolase by fluorescent based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50196658(12-(3-adamantan-1-yl-ureido)-dodecanoic acid tert-...)
Affinity DataIC50:  1.30nMAssay Description:Inhibition of human soluble epoxide hydrolase by fluorescent based assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217456(CHEMBL243337 | cis-1-adamantan-1-yl-3-[4-(4-bromop...)
Affinity DataIC50:  1.30nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50217448(CHEMBL242459 | US9029401, 1471 (t-AUCB) | trans-4-...)
Affinity DataIC50:  1.30nMAssay Description:Inhibition of human recombinant soluble epoxide hydrolaseMore data for this Ligand-Target Pair
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