TargetProthrombin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute
Curated by ChEMBL
Bristol-Myers Squibb Pharmaceutical Research Institute
Curated by ChEMBL
Affinity DataKi: 0.460nMAssay Description:Competitive kinetic for thrombin inhibition Ki was determinedMore data for this Ligand-Target Pair
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
TargetProthrombin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute
Curated by ChEMBL
Bristol-Myers Squibb Pharmaceutical Research Institute
Curated by ChEMBL
Affinity DataKi: 8.20nMAssay Description:Competitive kinetic for human alpha thrombin inhibition Ki was determinedMore data for this Ligand-Target Pair
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
TargetThromboxane A2 receptor(Homo sapiens (Human))
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Squibb Institute For Medical Research
Curated by PDSP Ki Database
Affinity DataIC50: 0.600nMAssay Description:Inhibition of protein kinase C etaMore data for this Ligand-Target Pair
Affinity DataIC50: 0.600nMAssay Description:PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.More data for this Ligand-Target Pair
Affinity DataIC50: 0.600nMpH: 7.5 T: 2°CAssay Description:PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.More data for this Ligand-Target Pair
Affinity DataIC50: 0.900nMpH: 7.5 T: 2°CAssay Description:PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.More data for this Ligand-Target Pair
Affinity DataIC50: 0.900nMAssay Description:Inhibition of protein kinase C deltaMore data for this Ligand-Target Pair
Affinity DataIC50: 0.900nMAssay Description:PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.More data for this Ligand-Target Pair
Affinity DataIC50: 1nMAssay Description:Inhibition of Protein kinase C etaMore data for this Ligand-Target Pair
Affinity DataIC50: 1nMAssay Description:Inhibition of src kinaseMore data for this Ligand-Target Pair
Affinity DataIC50: 1nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C eta isozymeMore data for this Ligand-Target Pair
Affinity DataIC50: 1nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C delta isozymeMore data for this Ligand-Target Pair
Affinity DataIC50: 1nMAssay Description:Inhibition of Protein kinase C deltaMore data for this Ligand-Target Pair
Affinity DataIC50: 1nMAssay Description:Inhibition of Hsp90 in human A375 cells assessed as pS6 degradation after 24 hrs by high content screeningMore data for this Ligand-Target Pair
Affinity DataIC50: 2nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C beta 2 isozymeMore data for this Ligand-Target Pair
TargetProthrombin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute
Curated by ChEMBL
Bristol-Myers Squibb Pharmaceutical Research Institute
Curated by ChEMBL
Affinity DataIC50: 2nMAssay Description:In vitro inhibitory activity against hydrolysis of thrombin was determinedMore data for this Ligand-Target Pair
Affinity DataIC50: 2nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C eta isozymeMore data for this Ligand-Target Pair
TargetProthrombin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute
Curated by ChEMBL
Bristol-Myers Squibb Pharmaceutical Research Institute
Curated by ChEMBL
Affinity DataIC50: 2nMAssay Description:In vitro inhibitory activity against hydrolysis of human alpha thrombinMore data for this Ligand-Target Pair
Affinity DataIC50: 2nMAssay Description:Inhibition of Hsp90 in human A375 cells assessed as Hsp70 induction after 24 hrs by high content screeningMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C beta 2 isozymeMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C eta isozymeMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibition of Protein kinase C etaMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C eta isozymeMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C eta isozymeMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C eta isozymeMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibition of Hsp90 in human AU565 cells assessed as Her2 degradation after 24 hrs by high content screeningMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibition of Protein kinase C zetaMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibition of Protein kinase C beta 2More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C eta isozymeMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibition of Protein kinase C etaMore data for this Ligand-Target Pair
Affinity DataIC50: 4nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C delta isozymeMore data for this Ligand-Target Pair
Affinity DataIC50: 4nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C eta isozymeMore data for this Ligand-Target Pair