TargetMu-type opioid receptor(Rattus norvegicus (rat))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetDelta-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetKappa-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetKappa-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetKappa-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetDelta-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetDelta-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetDelta-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetKappa-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetMu-type opioid receptor(Rattus norvegicus (rat))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetKappa-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetDelta-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetKappa-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetDelta-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetKappa-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetDelta-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetDelta-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetKappa-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetKappa-type opioid receptor(Homo sapiens (Human))
University of Maryland
Curated by PDSP Ki Database
University of Maryland
Curated by PDSP Ki Database
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 0.200nMAssay Description:Inhibition of BTK (unknown origin)More data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 0.200nMAssay Description:Inhibition of BTK (unknown origin)More data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 0.300nMAssay Description:Inhibition of BTK (unknown origin)More data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 0.390nMAssay Description:Inhibition of BTK C481S mutant (unknown origin)More data for this Ligand-Target Pair
TargetCytoplasmic tyrosine-protein kinase BMX(Homo sapiens (Human))
Peking University
Curated by ChEMBL
Peking University
Curated by ChEMBL
Affinity DataIC50: 0.710nMAssay Description:Inhibition of Bmx (unknown origin) after 1 hr by HTRF assayMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 0.720nMAssay Description:Inhibition of His-tagged full-length recombinant wild-type human BTK (Ala2 to Ser659 residues) expressed in baculovirus infected insect cells incubat...More data for this Ligand-Target Pair
Affinity DataIC50: 0.800nMAssay Description:Inhibition of cathepsin E using MCA-KPILFFRLK(Dnp)-D-R-NH2 as substrate incubated for 10 to 15 mins prior to substrate addition measured every 5 min ...More data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 0.850nMAssay Description:Inhibition of wild-type BTK (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 0.900nMAssay Description:Inhibition of Lck (unknown origin) after 1 hr by HTRF assayMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 1.10nMAssay Description:Inhibition of BTK (unknown origin)More data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 1.40nMAssay Description:Inhibition of BTK (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 1.40nMAssay Description:Inhibition of Rlk (unknown origin) after 1 hr by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.90nMAssay Description:Inhibition of Rlk (unknown origin) after 1 hr by HTRF assayMore data for this Ligand-Target Pair
TargetCytoplasmic tyrosine-protein kinase BMX(Homo sapiens (Human))
Peking University
Curated by ChEMBL
Peking University
Curated by ChEMBL
Affinity DataIC50: 1.90nMAssay Description:Inhibition of Bmx (unknown origin) after 1 hr by HTRF assayMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 2.5nMAssay Description:Inhibition of BTK C481S mutant (unknown origin) expressed in baculovirus infected Sf9 insect cells incubated for 30 mins in presence of ATP by Microf...More data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 2.60nMAssay Description:Inhibition of His-tagged full-length recombinant wild-type human BTK (Ala2 to Ser659 residues) expressed in baculovirus infected insect cells incubat...More data for this Ligand-Target Pair
Affinity DataIC50: 2.70nMAssay Description:Inhibition of Blk (unknown origin) after 1 hr by HTRF assayMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 3nMAssay Description:Inhibition of BTK C481S mutant (unknown origin) expressed in baculovirus infected Sf9 insect cells incubated for 30 mins in presence of ATP by Microf...More data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Nanjing University Of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 3.20nMAssay Description:Inhibition of His-tagged full-length recombinant wild-type human BTK (Ala2 to Ser659 residues) expressed in baculovirus infected insect cells incubat...More data for this Ligand-Target Pair
TargetReceptor tyrosine-protein kinase erbB-4(Homo sapiens (Human))
Peking University
Curated by ChEMBL
Peking University
Curated by ChEMBL
Affinity DataIC50: 3.30nMAssay Description:Inhibition of HER4 (unknown origin) after 1 hr by HTRF assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Xinxiang Medical University
Curated by ChEMBL
Xinxiang Medical University
Curated by ChEMBL
Affinity DataIC50: 3.60nMAssay Description:Inhibition of TNF-alpha release was determined in LPS-stimulated human whole blood assayMore data for this Ligand-Target Pair
Affinity DataIC50: 4nMAssay Description:Inhibition of Lck (unknown origin) after 1 hr by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 4nMAssay Description:Inhibition of Lck (unknown origin) after 1 hr by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 4nMAssay Description:Inhibition of Lck (unknown origin) after 1 hr by HTRF assayMore data for this Ligand-Target Pair