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Found 1193 with Last Name = 'jorgensen' and Initial = 'wl'
TargetProthrombin(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50098242(3-[4-(Amino-hydrazino-methyl)-phenyl]-N-cyclopenty...)
Affinity DataKi:  0.0450nMAssay Description:Binding affinity was determined against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50098232(3-[4-(Amino-hydrazino-methyl)-phenyl]-2-(anthracen...)
Affinity DataKi:  0.100nMAssay Description:Binding affinity was determined against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50098243(3-[4-(Amino-hydrazino-methyl)-phenyl]-N-cyclopenty...)
Affinity DataKi:  0.120nMAssay Description:Binding affinity was determined against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163152(1-Oxazolo[4,5-b]pyridin-2-yl-octadec-9-yn-1-one | ...)
Affinity DataKi:  0.140nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50161518(1-(oxazolo[4,5-b]pyridin-2-yl)-6-phenylhexan-1-one...)
Affinity DataKi:  0.200nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM23316(7-phenyl-1-{pyrido[2,3-d][1,3]oxazol-2-yl}heptan-1...)
Affinity DataKi:  0.280nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50098245(3-[4-(Amino-hydrazino-methyl)-phenyl]-N-cyclopenty...)
Affinity DataKi:  0.300nMAssay Description:Binding affinity was determined against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50098235(3-[4-(Amino-hydrazino-methyl)-phenyl]-N-cyclopenty...)
Affinity DataKi:  0.380nMAssay Description:Binding affinity was determined against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Bos taurus (Bovine))
Yale University

Curated by ChEMBL
LigandPNGBDBM50098235(3-[4-(Amino-hydrazino-methyl)-phenyl]-N-cyclopenty...)
Affinity DataKi:  1.10nMAssay Description:Binding affinity was determined against bovine thrombin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Bos taurus (Bovine))
Yale University

Curated by ChEMBL
LigandPNGBDBM50098236(CHEMBL9415 | Naphthalene-2-sulfonic acid {1-[4-(am...)
Affinity DataKi:  1.5nMAssay Description:Binding affinity was determined against bovine thrombin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50066638(3-[6-(5-Carbamimidoyl-2-hydroxy-phenoxy)-3,5-diflu...)
Affinity DataKi:  1.80nMAssay Description:Inhibition of human Coagulation factor X was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163165(1-(5-(pyridin-2-yl)oxazol-2-yl)dodecan-1-one | 1-(...)
Affinity DataKi:  2.20nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163177(7-Phenyl-1-(5-pyrimidin-4-yl-oxazol-2-yl)-heptan-1...)
Affinity DataKi:  2.30nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50066637(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-[3-(1-meth...)
Affinity DataKi:  2.40nMAssay Description:Inhibition of human Coagulation factor X was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Yale University

Curated by ChEMBL
LigandPNGBDBM2483((4S)-6-chloro-4-(2-cyclopropylethynyl)-4-(trifluor...)
Affinity DataKi:  3nMAssay Description:Effective concentration required against L100I mutant HIV-1 reverse transcriptase (as per ref 8 in the article)More data for this Ligand-Target Pair
TargetCoagulation factor X(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50113913(3-[6-(3-Dimethylamino-phenoxy)-3,5-difluoro-4-meth...)
Affinity DataKi:  3nMAssay Description:Inhibition of human Coagulation factor X was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50098237(2-{4-[2-(Cyclopentyl-methyl-carbamoyl)-2-(naphthal...)
Affinity DataKi:  3.30nMAssay Description:Binding affinity was determined against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163174(1-(5-Pyridin-2-yl-oxazol-2-yl)-undecan-1-one | CHE...)
Affinity DataKi:  3.30nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50098244(3-[4-(Amino-hydrazino-methyl)-phenyl]-N-cyclopenty...)
Affinity DataKi:  3.80nMAssay Description:Binding affinity was determined against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163207(7-Phenyl-1-(5-pyrimidin-2-yl-oxazol-2-yl)-heptan-1...)
Affinity DataKi:  4.60nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163186(1-(5-(oxazol-2-yl)oxazol-2-yl)-7-phenylheptan-1-on...)
Affinity DataKi:  4.60nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM23120(7-phenyl-1-[5-(pyridin-2-yl)-1,3-oxazol-2-yl]hepta...)
Affinity DataKi:  4.70nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163202(7-Phenyl-1-(5-pyrazin-2-yl-oxazol-2-yl)-heptan-1-o...)
Affinity DataKi:  5.30nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163213(7-Phenyl-1-(5-pyridazin-3-yl-oxazol-2-yl)-heptan-1...)
Affinity DataKi:  5.60nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163164(7-Phenyl-1-(5-thiazol-2-yl-oxazol-2-yl)-heptan-1-o...)
Affinity DataKi:  5.80nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50113894(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-(3-carbami...)
Affinity DataKi:  6nMAssay Description:Inhibition of human Coagulation factor X was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Bos taurus (Bovine))
Yale University

Curated by ChEMBL
LigandPNGBDBM50098230(CHEMBL9491 | N-[1-(4-Diaminomethyl-benzyl)-2-oxo-2...)
Affinity DataKi:  6.5nMAssay Description:Binding affinity was determined against bovine thrombin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM23334(3-(pyridin-3-yl)propyl (2S)-1-(3,3-dimethyl-2-oxop...)
Affinity DataKi:  7.5nMAssay Description:The compound was tested for binding affinity against rotamaseMore data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50161519(8-Phenyl-1-(5-pyridin-2-yl-oxazol-2-yl)-octan-1-on...)
Affinity DataKi:  7.5nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50161523(9-Phenyl-1-(5-pyridin-2-yl-oxazol-2-yl)-nonan-1-on...)
Affinity DataKi:  7.80nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50113925(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-[3-(2-meth...)
Affinity DataKi:  8nMAssay Description:Inhibition of human Coagulation factor X was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50098241(3-[4-(Amino-hydrazino-methyl)-phenyl]-N-cyclopenty...)
Affinity DataKi:  8nMAssay Description:Binding affinity was determined against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50113883(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-[3-(1,4-di...)
Affinity DataKi:  8.40nMAssay Description:Inhibition of human Coagulation factor X was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM23120(7-phenyl-1-[5-(pyridin-2-yl)-1,3-oxazol-2-yl]hepta...)
Affinity DataKi:  9nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from human expressed in COS-7 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50066636(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-[3-(1-meth...)
Affinity DataKi:  9nMAssay Description:Inhibition of human Coagulation factor X was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163167(1-(5-Pyridin-2-yl-oxazol-2-yl)-decan-1-one | CHEMB...)
Affinity DataKi:  9nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163159(1-(5-Pyridin-2-yl-oxazol-2-yl)-octadec-9-yn-1-one ...)
Affinity DataKi:  10nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataKi:  10nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from human expressed in COS-7 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163156(10-Phenyl-1-(5-pyridin-2-yl-oxazol-2-yl)-decan-1-o...)
Affinity DataKi:  10nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163157(1-(5-Pyridin-2-yl-oxazol-2-yl)-dec-9-en-1-one | CH...)
Affinity DataKi:  11nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50161517(6-Phenyl-1-(5-pyridin-2-yl-oxazol-2-yl)-hexan-1-on...)
Affinity DataKi:  11nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50098233(CHEMBL9461 | Naphthalene-2-sulfonic acid [1-[4-(am...)
Affinity DataKi:  11nMAssay Description:Binding affinity was determined against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163180((Z)-1-(5-(oxazol-2-yl)oxazol-2-yl)octadec-9-en-1-o...)
Affinity DataKi:  12nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50157136(1-(5-(furan-2-yl)oxazol-2-yl)-7-phenylheptan-1-one...)
Affinity DataKi:  12nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50113909(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-[3-(4-meth...)
Affinity DataKi:  13nMAssay Description:Inhibition of human Coagulation factor X was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163168(1-(5-Pyridin-2-yl-oxazol-2-yl)-tetradecan-1-one | ...)
Affinity DataKi:  13nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163173((Z)-1-(5-Pyridazin-3-yl-oxazol-2-yl)-octadec-9-en-...)
Affinity DataKi:  14nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMacrophage migration inhibitory factor(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50206092(CHEMBL3917143 | US10336721, Example 32 | US1096819...)
Affinity DataKi:  14nMAssay Description:Inhibition of recombinant human MIF tautomerase activity expressed in Escherichia coli assessed as borate-enol complex formation using 4-hydroxypheny...More data for this Ligand-Target Pair
TargetCoagulation factor X(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50066627(3-[6-(2-Amino-5-carbamimidoyl-phenoxy)-3,5-difluor...)
Affinity DataKi:  14nMAssay Description:Inhibition of human Coagulation factor X was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50163179(1-(5-Pyridin-2-yl-oxazol-2-yl)-nonan-1-one | CHEMB...)
Affinity DataKi:  15nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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