Compile Data Set for Download or QSAR
maximum 50k data
Found 1459 with Last Name = 'tsai' and Initial = 'h'
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50173419((3R,3aS,4S,4aR,8aS,9aR)-3-Methyl-4-{(E)-2-[5-(3-tr...)
Affinity DataKi:  2.70nMAssay Description:Inhibitory constant aganist Protease-activated receptor 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50020132(CHEMBL3288437)
Affinity DataKi:  5.10nMAssay Description:Displacement of [3H]haTRAP from PAR-1 receptor in human platelet membranes after 1 hr by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50020139(CHEMBL3288441)
Affinity DataKi:  8.90nMAssay Description:Displacement of [3H]haTRAP from PAR-1 receptor in human platelet membranes after 1 hr by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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
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
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50202073((3R,3aS,4S,4aR,7R,8aR,9aR)-decahydro-7-hydroxy-3-m...)
Affinity DataKi:  11nMAssay Description:Displacement of [3H]haTRAP from PAR1 in human platelet membraneMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50173417((3R,3aS,4S,4aR,8aS,9aR)-4-(2-(6-ethylpyridin-2-yl)...)
Affinity DataKi:  12nMAssay Description:Inhibitory constant aganist Protease-activated receptor 1More 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
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50020129(CHEMBL3288436)
Affinity DataKi:  16nMAssay Description:Displacement of [3H]haTRAP from PAR-1 receptor in human platelet membranes after 1 hr by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50020128(CHEMBL3288435)
Affinity DataKi:  21nMAssay Description:Displacement of [3H]haTRAP from PAR-1 receptor in human platelet membranes after 1 hr by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50020143(CHEMBL3288443)
Affinity DataKi:  25nMAssay Description:Displacement of [3H]haTRAP from PAR-1 receptor in human platelet membranes after 1 hr by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50020134(CHEMBL3288439)
Affinity DataKi:  27nMAssay Description:Displacement of [3H]haTRAP from PAR-1 receptor in human platelet membranes after 1 hr by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50020135(CHEMBL3288440)
Affinity DataKi:  28nMAssay Description:Displacement of [3H]haTRAP from PAR-1 receptor in human platelet membranes after 1 hr by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50020147(CHEMBL3288445)
Affinity DataKi:  32nMAssay Description:Displacement of [3H]haTRAP from PAR-1 receptor in human platelet membranes after 1 hr by scintillation counting analysisMore 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
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
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50020140(CHEMBL3288442)
Affinity DataKi:  43nMAssay Description:Displacement of [3H]haTRAP from PAR-1 receptor in human platelet membranes after 1 hr by scintillation counting analysisMore 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
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
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
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50020146(CHEMBL3288444)
Affinity DataKi:  232nMAssay Description:Displacement of [3H]haTRAP from PAR-1 receptor in human platelet membranes after 1 hr by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50020133(CHEMBL3288438)
Affinity DataKi:  267nMAssay Description:Displacement of [3H]haTRAP from PAR-1 receptor in human platelet membranes after 1 hr by scintillation counting analysisMore 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
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
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
TargetProteinase-activated receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50020148(CHEMBL3288446)
Affinity DataKi:  392nMAssay Description:Displacement of [3H]haTRAP from PAR-1 receptor in human platelet membranes after 1 hr by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50215908((3R,3aS,4S,4aR,8aS,9aR,E)-3-methyl-4-(2-(5-(pyrrol...)
Affinity DataKi:  487nMAssay Description:Binding affinity to cannabinoid CB2 receptorMore 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
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
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
TargetCannabinoid receptor 2(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50215910((3R,3aS,4S,4aR,8aS,9aR,E)-3-methyl-4-(2-(5-(pyridi...)
Affinity DataKi:  1.30E+4nMAssay Description:Binding affinity to cannabinoid CB2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldehyde oxidase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50366979(PYRIDOXAL)
Affinity DataKi:  3.00E+4nMAssay Description:Tested for its ability to inhibit rabbit liver aldehyde oxidase catalyzed oxidation of N-methyl-nicotinamide (NMN)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldehyde oxidase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50366978(CHEMBL103375)
Affinity DataKi:  1.00E+5nMAssay Description:Tested for its ability to inhibit rabbit liver aldehyde oxidase catalyzed oxidation of N-methyl-nicotinamide (NMN)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldehyde oxidase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50366982(CHEMBL316980)
Affinity DataKi:  2.00E+5nMAssay Description:Tested for its ability to inhibit rabbit liver aldehyde oxidase catalyzed oxidation of N-methyl-nicotinamide (NMN)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldehyde oxidase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50366976(CHEMBL102691)
Affinity DataKi:  2.00E+5nMAssay Description:Tested for its ability to inhibit rabbit liver aldehyde oxidase catalyzed oxidation of N-methyl-nicotinamide (NMN)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldehyde oxidase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50366977(CHEMBL103253)
Affinity DataKi:  3.00E+5nMAssay Description:Tested for its ability to inhibit rabbit liver aldehyde oxidase catalyzed oxidation of N-methyl-nicotinamide (NMN)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldehyde oxidase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50366980(CHEMBL318466)
Affinity DataKi:  3.00E+5nMAssay Description:Tested for its ability to inhibit rabbit liver aldehyde oxidase catalyzed oxidation of N-methyl-nicotinamide (NMN)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldehyde oxidase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50366981(CHEMBL318547)
Affinity DataKi:  4.00E+5nMAssay Description:Tested for its ability to inhibit rabbit liver aldehyde oxidase catalyzed oxidation of N-methyl-nicotinamide (NMN)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldehyde oxidase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50366975(CHEMBL105079)
Affinity DataKi:  1.50E+6nMAssay Description:Tested for its ability to inhibit rabbit liver aldehyde oxidase catalyzed oxidation of N-methyl-nicotinamide (NMN)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:  0.0200nMAssay 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 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
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
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
TargetAurora kinase A(Homo sapiens (Human))
Taiwan National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50241089(2-(ethyl(3-(4-(5-(2-(3-fluorophenylamino)-2-oxoeth...)
Affinity DataIC50:  0.370nMAssay Description:Inhibition of recombinant GST-tagged N-terminal truncated human Aurora A (123 to 401 residues) expressed in Sf9 insect cell using tetra-LRRASLG pepti...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEpoxide hydrolase 1(Homo sapiens (Human))
The Regents of The University of California

US Patent
LigandPNGBDBM50327847(1-(1-(Trifluoroacetyl)piperidin-4-yl)-3-(4-(triflu...)
Affinity DataIC50:  0.400nMAssay Description:Inhibition assay of human soluble epoxide hydrolases.More data for this Ligand-Target Pair
In DepthDetails US Patent
Displayed 1 to 50 (of 1459 total ) | Next | Last >>
Jump to: