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Found 104 with Last Name = 'woltmann' and Initial = 'rf'
TargetProthrombin(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060708((S)-1-(3-Benzo[1,3]dioxol-5-yl-3-pyridin-3-yl-prop...)
Affinity DataKi:  0.280nM Koff:  2.51E+3s-1Assay Description:Inhibition of ThrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060705((S)-1-(3,3-Diphenyl-propionyl)-pyrrolidine-2-carbo...)
Affinity DataKi:  2nM Koff:  2.10E+3s-1Assay Description:Inhibition of ThrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060704((S)-1-(2-5H-Dibenzo[a,d]cyclohepten-5-yl-acetyl)-p...)
Affinity DataKi:  3nM Koff:  1.80E+3s-1Assay Description:Inhibition of ThrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060703((S)-1-(3-Phenyl-3-pyridin-4-yl-propionyl)-pyrrolid...)
Affinity DataKi:  3.40nM Koff:  1.55E+3s-1Assay Description:Inhibition of ThrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060706((S)-1-(3-Cyclohexyl-3-phenyl-propionyl)-pyrrolidin...)
Affinity DataKi:  8nMAssay Description:Inhibition of ThrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060707((S)-1-(3-Phenyl-3-pyridin-3-yl-propionyl)-pyrrolid...)
Affinity DataKi:  10nM Koff:  2.10E+3s-1Assay Description:Inhibition of ThrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060709((S)-1-(3-Phenyl-3-pyridin-2-yl-propionyl)-pyrrolid...)
Affinity DataKi:  12nM Koff:  1.80E+3s-1Assay Description:Inhibition of ThrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060711((S)-1-(3,3-Dicyclohexyl-propionyl)-pyrrolidine-2-c...)
Affinity DataKi:  14nM Koff:  2.30E+3s-1Assay Description:Inhibition of ThrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060710((S)-1-(3,3-Diphenyl-butyryl)-pyrrolidine-2-carboxy...)
Affinity DataKi:  16nMAssay Description:Inhibition of ThrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060712((S)-1-(2-10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-...)
Affinity DataKi:  17nMAssay Description:Inhibition of ThrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060705((S)-1-(3,3-Diphenyl-propionyl)-pyrrolidine-2-carbo...)
Affinity DataKi:  350nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060704((S)-1-(2-5H-Dibenzo[a,d]cyclohepten-5-yl-acetyl)-p...)
Affinity DataKi:  1.60E+3nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060706((S)-1-(3-Cyclohexyl-3-phenyl-propionyl)-pyrrolidin...)
Affinity DataKi:  1.70E+3nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060703((S)-1-(3-Phenyl-3-pyridin-4-yl-propionyl)-pyrrolid...)
Affinity DataKi:  2.20E+3nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060711((S)-1-(3,3-Dicyclohexyl-propionyl)-pyrrolidine-2-c...)
Affinity DataKi:  2.50E+3nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060708((S)-1-(3-Benzo[1,3]dioxol-5-yl-3-pyridin-3-yl-prop...)
Affinity DataKi:  2.60E+3nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060707((S)-1-(3-Phenyl-3-pyridin-3-yl-propionyl)-pyrrolid...)
Affinity DataKi:  2.80E+3nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060709((S)-1-(3-Phenyl-3-pyridin-2-yl-propionyl)-pyrrolid...)
Affinity DataKi:  5.00E+3nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060710((S)-1-(3,3-Diphenyl-butyryl)-pyrrolidine-2-carboxy...)
Affinity DataKi:  1.70E+4nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060711((S)-1-(3,3-Dicyclohexyl-propionyl)-pyrrolidine-2-c...)
Affinity DataKi:  8.40E+4nMAssay Description:Inhibitory activity against serine protease TPAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasma kallikrein(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060711((S)-1-(3,3-Dicyclohexyl-propionyl)-pyrrolidine-2-c...)
Affinity DataKi:  1.70E+5nMAssay Description:Inhibitory activity against serine protease plasma kallikreinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060711((S)-1-(3,3-Dicyclohexyl-propionyl)-pyrrolidine-2-c...)
Affinity DataKi:  1.76E+5nMAssay Description:Inhibitory activity against serine protease plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060711((S)-1-(3,3-Dicyclohexyl-propionyl)-pyrrolidine-2-c...)
Affinity DataKi:  2.20E+5nMAssay Description:Inhibitory activity against serine protease Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060704((S)-1-(2-5H-Dibenzo[a,d]cyclohepten-5-yl-acetyl)-p...)
Affinity DataKi:  2.68E+5nMAssay Description:Inhibitory activity against serine protease TPAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060709((S)-1-(3-Phenyl-3-pyridin-2-yl-propionyl)-pyrrolid...)
Affinity DataKi:  3.70E+5nMAssay Description:Inhibitory activity against serine protease Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060703((S)-1-(3-Phenyl-3-pyridin-4-yl-propionyl)-pyrrolid...)
Affinity DataKi:  4.00E+5nMAssay Description:Inhibitory activity against serine protease Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060704((S)-1-(2-5H-Dibenzo[a,d]cyclohepten-5-yl-acetyl)-p...)
Affinity DataKi:  4.14E+5nMAssay Description:Inhibitory activity against serine protease plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060703((S)-1-(3-Phenyl-3-pyridin-4-yl-propionyl)-pyrrolid...)
Affinity DataKi:  4.36E+5nMAssay Description:Inhibitory activity against serine protease TPAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasma kallikrein(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060707((S)-1-(3-Phenyl-3-pyridin-3-yl-propionyl)-pyrrolid...)
Affinity DataKi:  4.76E+5nMAssay Description:Inhibitory activity against serine protease plasma kallikreinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060708((S)-1-(3-Benzo[1,3]dioxol-5-yl-3-pyridin-3-yl-prop...)
Affinity DataKi: >5.00E+5nMAssay Description:Inhibitory activity against serine protease TPAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060708((S)-1-(3-Benzo[1,3]dioxol-5-yl-3-pyridin-3-yl-prop...)
Affinity DataKi:  5.72E+5nMAssay Description:Inhibitory activity against serine protease plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060705((S)-1-(3,3-Diphenyl-propionyl)-pyrrolidine-2-carbo...)
Affinity DataKi:  7.44E+5nMAssay Description:Inhibitory activity against serine protease plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060703((S)-1-(3-Phenyl-3-pyridin-4-yl-propionyl)-pyrrolid...)
Affinity DataKi:  7.44E+5nMAssay Description:Inhibitory activity against serine protease plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060707((S)-1-(3-Phenyl-3-pyridin-3-yl-propionyl)-pyrrolid...)
Affinity DataKi:  7.46E+5nMAssay Description:Inhibitory activity against serine protease TPAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasma kallikrein(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060709((S)-1-(3-Phenyl-3-pyridin-2-yl-propionyl)-pyrrolid...)
Affinity DataKi:  7.67E+5nMAssay Description:Inhibitory activity against serine protease plasma kallikreinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasma kallikrein(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060704((S)-1-(2-5H-Dibenzo[a,d]cyclohepten-5-yl-acetyl)-p...)
Affinity DataKi:  7.75E+5nMAssay Description:Inhibitory activity against serine protease plasma kallikreinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060705((S)-1-(3,3-Diphenyl-propionyl)-pyrrolidine-2-carbo...)
Affinity DataKi:  9.80E+5nMAssay Description:Inhibitory activity against serine protease Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060704((S)-1-(2-5H-Dibenzo[a,d]cyclohepten-5-yl-acetyl)-p...)
Affinity DataKi: >1.00E+6nMAssay Description:Inhibitory activity against serine protease Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasma kallikrein(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060705((S)-1-(3,3-Diphenyl-propionyl)-pyrrolidine-2-carbo...)
Affinity DataKi: >1.00E+6nMAssay Description:Inhibitory activity against serine protease plasma kallikreinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060708((S)-1-(3-Benzo[1,3]dioxol-5-yl-3-pyridin-3-yl-prop...)
Affinity DataKi:  1.00E+6nMAssay Description:Inhibitory activity against serine protease Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060707((S)-1-(3-Phenyl-3-pyridin-3-yl-propionyl)-pyrrolid...)
Affinity DataKi: >1.00E+6nMAssay Description:Inhibitory activity against serine protease plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060707((S)-1-(3-Phenyl-3-pyridin-3-yl-propionyl)-pyrrolid...)
Affinity DataKi: >1.00E+6nMAssay Description:Inhibitory activity against serine protease Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060709((S)-1-(3-Phenyl-3-pyridin-2-yl-propionyl)-pyrrolid...)
Affinity DataKi: >1.00E+6nMAssay Description:Inhibitory activity against serine protease TPAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060705((S)-1-(3,3-Diphenyl-propionyl)-pyrrolidine-2-carbo...)
Affinity DataKi: >1.00E+6nMAssay Description:Inhibitory activity against serine protease TPAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasma kallikrein(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060703((S)-1-(3-Phenyl-3-pyridin-4-yl-propionyl)-pyrrolid...)
Affinity DataKi: >1.00E+6nMAssay Description:Inhibitory activity against serine protease plasma kallikreinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasma kallikrein(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060708((S)-1-(3-Benzo[1,3]dioxol-5-yl-3-pyridin-3-yl-prop...)
Affinity DataKi:  1.00E+6nMAssay Description:Inhibitory activity against serine protease plasma kallikreinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060709((S)-1-(3-Phenyl-3-pyridin-2-yl-propionyl)-pyrrolid...)
Affinity DataKi: >1.00E+6nMAssay Description:Inhibitory activity against serine protease plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50252711(3,5-Dichloro-N-{[(3S,4R)-1-(3,3-dimethylbutyl)-3-f...)
Affinity DataIC50: <20nMAssay Description:Inhibition of sigma1 opioid receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVoltage-dependent T-type calcium channel subunit alpha-1I(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50252709(CHEMBL493467 | N-({1-[2-(tert-butylamino)-2-oxoeth...)
Affinity DataIC50:  22nMAssay Description:Inhibition of T-type calcium channel alpha1I (unknown origin) by FLIPRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVoltage-dependent T-type calcium channel subunit alpha-1G(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50252711(3,5-Dichloro-N-{[(3S,4R)-1-(3,3-dimethylbutyl)-3-f...)
Affinity DataIC50:  25nMAssay Description:Inhibition of human T-type Cav3.1 expressed in HEK293 cells at -80mV holding potential by whole cell patch clamp assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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