Compile Data Set for Download or QSAR
Found 3814 of ic50 for UniProtKB: P00734
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50125842(5-amino(imino)methylamino-2-[1-[2-amino-3-phenyl-(...)copy SMILEScopy InChI
Affinity DataIC50: 0.00170nMAssay Description:In vitro inhibitory concentration of compound against human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NG4RCWPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50120225(2-{[2-(4-Guanidino-butyrylamino)-3-(4-nitro-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.00800nMAssay Description:Concentration of the compound required to inhibit thrombin was determinedMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20P0ZBKPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254888(US9493472, 11)copy SMILEScopy InChI
Affinity DataIC50: 0.0100nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50228863((S)-1-((R)-2-Methylamino-3-phenyl-propionyl)-pyrro...)copy SMILEScopy InChI
Affinity DataIC50: 0.0300nMAssay Description:Concentration of the compound required to inhibit thrombin was determinedMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20P0ZBKPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50063555(1-(2-Amino-3,3-diphenyl-propionyl)-pyrrolidine-2-c...)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibitory activity against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6RCFPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254889(US9493472, 12)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50096624(3-(4-Amino-cyclohexyl)-2-oxo-3-[((6S,8aS)-4-oxo-2-...)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:In vitro activity of the compound against human alpha thrombin was determinedMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2P55MS6PubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50520683(CHEMBL4476621)copy SMILEScopy InChI
Affinity DataIC50: 0.103nMAssay Description:Inhibition of human thrombin using Z-GPR-AMC as substrate after 30 mins by fluorimetric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4GNDPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254905(US9493472, 27)copy SMILEScopy InChI
Affinity DataIC50: 0.160nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50443853(CHEMBL3091519 | US20230391761, Reference 1)copy SMILEScopy InChI
Affinity DataIC50: 0.190nMMore data for this Ligand-Target Pair
In DepthDetails
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254904(US9493472, 26)copy SMILEScopy InChI
Affinity DataIC50: 0.190nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254886(US9493472, 9)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254896(US9493472, 18)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254895(US9493472, 17)copy SMILEScopy InChI
Affinity DataIC50: 0.370nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254911(US9493472, 33)copy SMILEScopy InChI
Affinity DataIC50: 0.380nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50289560(CHEMBL289389 | N-((S)-1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 0.467nMAssay Description:Inhibitory concentration of the compound required to inhibit human thrombin enzyme was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VNX
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254894(US9493472, 16)copy SMILEScopy InChI
Affinity DataIC50: 0.470nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50076074(1N-[1-amino(imino)methyl-6-hydroxy-(5S)-tetrahydro...)copy SMILEScopy InChI
Affinity DataIC50: 0.505nMAssay Description:Concentration required for the in vitro inhibitory activity against human enzyme, thrombin cleavage of the chromogenic substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NS0T3QPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50076074(1N-[1-amino(imino)methyl-6-hydroxy-(5S)-tetrahydro...)copy SMILEScopy InChI
Affinity DataIC50: 0.505nMAssay Description:Inhibitory concentration of the compound required to inhibit human thrombin enzyme was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7VNX
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254907(US9493472, 29 | US9493472, 30 | US9493472, 31)copy SMILEScopy InChI
Affinity DataIC50: 0.540nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50054486(CHEMBL141424 | N-[(S)-1-((S)-1-Carbamimidoyl-piper...)copy SMILEScopy InChI
Affinity DataIC50: 0.670nMAssay Description:Compound was evaluated for inhibition of amidolytic activity for chromogenic substrate thrombin F11a.More data for this Ligand-Target Pair
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254910(US9493472, 32)copy SMILEScopy InChI
Affinity DataIC50: 0.700nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50054498((R)-1-((R)-2-Methylamino-3-phenyl-propionyl)-pyrro...)copy SMILEScopy InChI
Affinity DataIC50: 0.700nMAssay Description:In vitro for inhibition of serine protease thrombin(FIIa).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28051QTPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50073429(CHEMBL82032 | CHEMBL84575 | N-((S)-1-Carbamimidoyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.710nMAssay Description:The compound was tested in vitro for inhibitory activity against Coagulation factor IIMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X92B91
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50073429(CHEMBL82032 | CHEMBL84575 | N-((S)-1-Carbamimidoyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.710nMAssay Description:In vitro inhibitory activity of the compound against human enzyme thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50054493(CHEMBL343805 | N-((S)-3-Carbamimidoyl-2-hydroxy-cy...)copy SMILEScopy InChI
Affinity DataIC50: 0.710nMAssay Description:In vitro for inhibition of serine protease thrombin(FIIa).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28051QTPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50054484(CHEMBL344204 | CVS-1778 | N-((S)-1-Formyl-4-guanid...)copy SMILEScopy InChI
Affinity DataIC50: 0.710nMAssay Description:Compound was evaluated for inhibition of amidolytic activity for chromogenic substrate thrombin F11a.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5SFVPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254892(US9493472, 15)copy SMILEScopy InChI
Affinity DataIC50: 0.720nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM639342(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-{[(5-chloro-2...)copy SMILES
Affinity DataIC50: 0.740nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM639341(2-(1-Methyl-1H-imidazol-5-yl)ethyl 3-[(5-chlorothi...)copy SMILES
Affinity DataIC50: 0.830nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50234836(CHEMBL4086267)copy SMILEScopy InChI
Affinity DataIC50: 0.840nMAssay Description:Inhibition of human thrombin preincubated for 10 mins followed by Ac-FVR-AMC substrate addition measured every 20s for 10 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HT2RK1PubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50287790((2S,4R)-1-Acetyl-4-benzyloxy-pyrrolidine-2-carboxy...)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W95963
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50191108(CHEMBL3974458)copy SMILEScopy InChI
Affinity DataIC50: 0.920nMAssay Description:Inhibition of human thrombin pre-incubated for 10 mins before Ac-FVR-AMC substrate addition and measured after 10 mins by fluorescence based assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3PF0PubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM176047(US10047103, 80 | US9688695, 80)copy SMILEScopy InChI
Affinity DataIC50: 0.940nMT: 2°CAssay Description:The ability of the compounds of the current invention to inhibit platelet aggregation induced by gamma-thrombin was tested in a 96-well microplate ag...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QF8VWNUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM176041(US10047103, 74 | US9688695, 74)copy SMILEScopy InChI
Affinity DataIC50: 0.960nMT: 2°CAssay Description:The ability of the compounds of the current invention to inhibit platelet aggregation induced by gamma-thrombin was tested in a 96-well microplate ag...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QF8VWNUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50114263(((R)-2-{(S)-2-[(5-Carbamimidoyl-thiophen-2-ylmethy...)copy SMILEScopy InChI
Affinity DataIC50: 0.980nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC90T5PubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM254897(US9493472, 19)copy SMILEScopy InChI
Affinity DataIC50: 0.980nMpH: 7.4 T: 2°CAssay Description:To determine the thrombin inhibition of the substances listed above, a biochemical test system is constructed in which the conversion of a thrombin s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56HPWUS Patent
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM652744(8-methyl-N-((2-((1-methylpiperidin-4-yl)methoxy)py...)copy SMILES
Ligand InfoPC cidPC sid
In DepthDetails
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM33812(1-[5-[(4-fluorobenzyl)amino]-3-(3-pyridyl)-1,2,4-t...)copy SMILEScopy InChI
Affinity DataIC50: 1nMpH: 7.5 T: 2°CAssay Description:HTS was performed using 217,350 compounds of the MLSCN library individually plated into 10ul 1536 compound plates at a concentration of 2.5 mM each, ...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2K64GDNPCBioAssay
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50543723(CHEMBL4640512)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of thrombin (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20P13M6PubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM32881(MLS000706208 | SMR000288260 | [3-(2-furanyl)-5-(me...)copy SMILEScopy InChI
Affinity DataIC50: 1nMpH: 7.5 T: 2°CAssay Description:HTS was performed using 217,350 compounds of the MLSCN library individually plated into 10ul 1536 compound plates at a concentration of 2.5 mM each, ...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2K64GDNPCBioAssay
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50217503(CHEMBL352928)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human ThrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25Q4V8VPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50076017((6S,8aS)-4-Oxo-2-(3-phenyl-propionyl)-octahydro-py...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human ThrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25Q4V8VPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM33836(3-(2-furyl)-1-(3-pyridinylcarbonyl)-N-(2-thienylme...)copy SMILEScopy InChI
Affinity DataIC50: 1nMpH: 7.5 T: 2°CAssay Description:HTS was performed using 217,350 compounds of the MLSCN library individually plated into 10ul 1536 compound plates at a concentration of 2.5 mM each, ...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2K64GDNPCBioAssay
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50072741((6S,8aS)-4-Oxo-2-(3-phenyl-propionyl)-octahydro-py...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:In vitro inhibitory activity against thrombin(FIIa)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27943VVPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50072741((6S,8aS)-4-Oxo-2-(3-phenyl-propionyl)-octahydro-py...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human alpha-thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21J9BNHPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50182201(((R)-2-{(S)-2-[(6-carbamimidoyl-pyridin-3-ylmethyl...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50114263(((R)-2-{(S)-2-[(5-Carbamimidoyl-thiophen-2-ylmethy...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of thrombin by chromogenic assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GM883VPubMed
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM50182198(((R)-2-{(S)-2-[(5-carbamimidoyl-thiophen-2-ylmethy...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of thrombin by chromogenic assayMore data for this Ligand-Target Pair
TargetProthrombin(Homo sapiens (Human))
Link£ping University

Curated by ChEMBL
LigandPNGBDBM176255(US10047103, 288 | US9688695, 288)copy SMILEScopy InChI
Affinity DataIC50: 1nMT: 2°CAssay Description:The ability of the compounds of the current invention to inhibit platelet aggregation induced by gamma-thrombin was tested in a 96-well microplate ag...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QF8VWNUS Patent
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