Compile Data Set for Download or QSAR
Found 92 with Last Name = 'coote' and Initial = 'sj'
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072292((3S,3aS,6aS)-3-Phenylsulfanyl-hexahydro-cyclopenta...)copy SMILEScopy InChI
Affinity DataIC50: 0.0200nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072285((3R,3aS,6aS)-3-Phenylsulfanyl-hexahydro-cyclopenta...)copy SMILEScopy InChI
Affinity DataIC50: 0.120nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072289((3S,3aR,6aS)-3-(4-Methyl-2-oxo-pent-3-enyl)-hexahy...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072283((3S,3aR,6aS)-3-Benzyl-hexahydro-cyclopenta[b]furan...)copy SMILEScopy InChI
Affinity DataIC50: 0.600nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072286((3R,3aR,6aS)-3-Benzyl-hexahydro-cyclopenta[b]furan...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072284((1S,2R,4aR,6aS,6bS,7R,9aS,10aS)-2-Acetoxy-1,4a,6a,...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072285((3R,3aS,6aS)-3-Phenylsulfanyl-hexahydro-cyclopenta...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072290((3S,3aR,6aS)-3-Allyl-hexahydro-cyclopenta[b]furan-...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50075121(5-[(3aS,8aS)-5-(4-Hydroxy-phenyl)-2-oxo-3,3a,8,8a-...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibitory activity of the compound against human thrombin was determinedMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26T0KS3PubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072292((3S,3aS,6aS)-3-Phenylsulfanyl-hexahydro-cyclopenta...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078554((3R,3aS,8aS)-3-(4-Carbamimidoyl-butyl)-6-(3-diethy...)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078544(3-[(3R,3aS,8aS)-1-Benzenesulfonyl-3-(4-carbamimido...)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072287((3S,6aS)-3-(4-Methyl-2-oxo-pent-3-enyl)-hexahydro-...)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072289((3S,3aR,6aS)-3-(4-Methyl-2-oxo-pent-3-enyl)-hexahy...)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072290((3S,3aR,6aS)-3-Allyl-hexahydro-cyclopenta[b]furan-...)copy SMILEScopy InChI
Affinity DataIC50: 26nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078554((3R,3aS,8aS)-3-(4-Carbamimidoyl-butyl)-6-(3-diethy...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072287((3S,6aS)-3-(4-Methyl-2-oxo-pent-3-enyl)-hexahydro-...)copy SMILEScopy InChI
Affinity DataIC50: 33nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072282((3R,3aR,6aS)-3-Allyl-hexahydro-cyclopenta[b]furan-...)copy SMILEScopy InChI
Affinity DataIC50: 37nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072293(5-((3R,3aR,6aS)-2-Oxo-hexahydro-cyclopenta[b]furan...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072282((3R,3aR,6aS)-3-Allyl-hexahydro-cyclopenta[b]furan-...)copy SMILEScopy InChI
Affinity DataIC50: 41nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072282((3R,3aR,6aS)-3-Allyl-hexahydro-cyclopenta[b]furan-...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078553((3R,3aS,8aS)-3-(4-Carbamimidoyl-butyl)-5-(3-diethy...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078544(3-[(3R,3aS,8aS)-1-Benzenesulfonyl-3-(4-carbamimido...)copy SMILEScopy InChI
Affinity DataIC50: 66nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072284((1S,2R,4aR,6aS,6bS,7R,9aS,10aS)-2-Acetoxy-1,4a,6a,...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072284((1S,2R,4aR,6aS,6bS,7R,9aS,10aS)-2-Acetoxy-1,4a,6a,...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Compound was evaluated for the inhibition of Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072283((3S,3aR,6aS)-3-Benzyl-hexahydro-cyclopenta[b]furan...)copy SMILEScopy InChI
Affinity DataIC50: 73nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Glaxo Wellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078544(3-[(3R,3aS,8aS)-1-Benzenesulfonyl-3-(4-carbamimido...)copy SMILEScopy InChI
Affinity DataIC50: 74nMAssay Description:Inhibition of activated Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50075122(5-((3aS,8aS)-2-Oxo-3,3a,8,8a-tetrahydro-2H-indeno[...)copy SMILEScopy InChI
Affinity DataIC50: 77nMAssay Description:Inhibitory activity of the compound against human thrombin was determinedMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26T0KS3PubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072286((3R,3aR,6aS)-3-Benzyl-hexahydro-cyclopenta[b]furan...)copy SMILEScopy InChI
Affinity DataIC50: 92nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072290((3S,3aR,6aS)-3-Allyl-hexahydro-cyclopenta[b]furan-...)copy SMILEScopy InChI
Affinity DataIC50: 98nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072289((3S,3aR,6aS)-3-(4-Methyl-2-oxo-pent-3-enyl)-hexahy...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072285((3R,3aS,6aS)-3-Phenylsulfanyl-hexahydro-cyclopenta...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072283((3S,3aR,6aS)-3-Benzyl-hexahydro-cyclopenta[b]furan...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072292((3S,3aS,6aS)-3-Phenylsulfanyl-hexahydro-cyclopenta...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072286((3R,3aR,6aS)-3-Benzyl-hexahydro-cyclopenta[b]furan...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Glaxo Wellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078554((3R,3aS,8aS)-3-(4-Carbamimidoyl-butyl)-6-(3-diethy...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibition of activated Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078552((3R,3aS,8aS)-3-(4-Carbamimidoyl-butyl)-5-(3-diethy...)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072293(5-((3R,3aR,6aS)-2-Oxo-hexahydro-cyclopenta[b]furan...)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:Inhibitory activity of the compound against human thrombin was determinedMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26T0KS3PubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072293(5-((3R,3aR,6aS)-2-Oxo-hexahydro-cyclopenta[b]furan...)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50072291(4-((3R,3aR,6aS)-2-Oxo-hexahydro-cyclopenta[b]furan...)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ105FPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078556(3-[(3R,3aS,8aS)-3-(4-Carbamimidoyl-butyl)-2-oxo-1-...)copy SMILEScopy InChI
Affinity DataIC50: 380nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50075123(4-((3R,3aS,8aS)-2-Oxo-3,3a,8,8a-tetrahydro-2H-inde...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:Inhibitory activity of the compound against human thrombin was determinedMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26T0KS3PubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078557((3R,3aS,8aS)-3-(4-Carbamimidoyl-butyl)-6-(3-diethy...)copy SMILEScopy InChI
Affinity DataIC50: 620nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078557((3R,3aS,8aS)-3-(4-Carbamimidoyl-butyl)-6-(3-diethy...)copy SMILEScopy InChI
Affinity DataIC50: 660nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50075120(5-[(3R,3aS,8aS)-5-(4-Hydroxy-phenyl)-2-oxo-3,3a,8,...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibitory activity of the compound against human thrombin was determinedMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26T0KS3PubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078551(CHEMBL46365 | [(3R,3aS,8aS)-3-(4-Carbamimidoyl-but...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078549((3R,3aS,8aS)-3-(4-Carbamimidoyl-butyl)-6-(3-diethy...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetProthrombin(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50075119(5-[(3aR,8aS)-6-(3-Methoxy-phenyl)-3-methyl-2-oxo-3...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibitory activity of the compound against human thrombin was determinedMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26T0KS3PubMed
TargetCoagulation factor X(Homo sapiens (Human))
Glaxo Wellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078553((3R,3aS,8aS)-3-(4-Carbamimidoyl-butyl)-5-(3-diethy...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of activated Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
TargetSerine protease 1(Homo sapiens (Human))
GlaxoWellcome Research and Development

Curated by ChEMBL
LigandPNGBDBM50078553((3R,3aS,8aS)-3-(4-Carbamimidoyl-butyl)-5-(3-diethy...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VT1R8QPubMed
Displayed 1 to 50 (of 92 total ) | Next | Last >>
Jump to: