TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Affinity DataIC50: 1.80nMAssay Description:Inhibition of c-Met (unknown origin) using poly (Glu, Tyr) 4:1 as substrate incubated for 30 mins by HTRF assayMore data for this Ligand-Target Pair
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Affinity DataIC50: 2.30nMAssay Description:Inhibition of c-Met (unknown origin) using poly (Glu, Tyr) 4:1 as substrate incubated for 30 mins by HTRF assayMore data for this Ligand-Target Pair
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Affinity DataIC50: 3.10nMAssay Description:Inhibition of c-Met (unknown origin) using poly (Glu, Tyr) 4:1 as substrate incubated for 30 mins by HTRF assayMore data for this Ligand-Target Pair
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Affinity DataIC50: 6.70nMAssay Description:Inhibition of c-Met (unknown origin) using poly (Glu, Tyr) 4:1 as substrate incubated for 30 mins by HTRF assayMore data for this Ligand-Target Pair
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Affinity DataIC50: 8.80nMAssay Description:Inhibition of c-Met (unknown origin) using poly (Glu, Tyr) 4:1 as substrate incubated for 30 mins by HTRF assayMore data for this Ligand-Target Pair
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Affinity DataIC50: 8.90nMAssay Description:Inhibition of FLT3 (unknown origin) using poly (Glu, Tyr) 4:1 as substrate incubated for 30 mins by HTRF assayMore data for this Ligand-Target Pair
TargetMast/stem cell growth factor receptor Kit(Homo sapiens (Human))
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Affinity DataIC50: 9.40nMAssay Description:Inhibition of c-kit (unknown origin) using poly (Glu, Tyr) 4:1 as substrate incubated for 30 mins by HTRF assayMore data for this Ligand-Target Pair
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Affinity DataIC50: 9.5nMAssay Description:Inhibition of c-Met (unknown origin) using poly (Glu, Tyr) 4:1 as substrate incubated for 30 mins by HTRF assayMore data for this Ligand-Target Pair
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Affinity DataIC50: 10nMAssay Description:Inhibition of c-Met (unknown origin) using poly (Glu, Tyr) 4:1 as substrate incubated for 30 mins by HTRF assayMore data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 35nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 53nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 97nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Affinity DataIC50: 97nMAssay Description:Inhibition of VEGFR2 (unknown origin) using poly (Glu, Tyr) 4:1 as substrate incubated for 30 mins by HTRF assayMore data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 97nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 108nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 110nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 118nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 5 mins followed by fluorogenic substrate addition measured after 30 mins by microplate reader a...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 120nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 5 mins followed by fluorogenic substrate addition measured after 30 mins by microplate reader a...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 125nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 127nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 129nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 5 mins followed by fluorogenic substrate addition measured after 30 mins by microplate reader a...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 131nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 5 mins followed by fluorogenic substrate addition measured after 30 mins by microplate reader a...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 131nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 135nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 137nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 5 mins followed by fluorogenic substrate addition measured after 30 mins by microplate reader a...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 154nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 5 mins followed by fluorogenic substrate addition measured after 30 mins by microplate reader a...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 154nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 169nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 5 mins followed by fluorogenic substrate addition measured after 30 mins by microplate reader a...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 173nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 5 mins followed by fluorogenic substrate addition measured after 30 mins by microplate reader a...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 178nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 5 mins followed by fluorogenic substrate addition measured after 30 mins by microplate reader a...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 184nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 217nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 5 mins followed by fluorogenic substrate addition measured after 30 mins by microplate reader a...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
The General Hospital Of Chinese People'S Liberation Army
Curated by ChEMBL
Affinity DataIC50: 273nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 5 mins followed by fluorogenic substrate addition measured after 30 mins by microplate reader a...More data for this Ligand-Target Pair
TargetMacrophage-stimulating protein receptor(Homo sapiens (Human))
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Affinity DataIC50: 346nMAssay Description:Inhibition of Ron (unknown origin) using poly (Glu, Tyr) 4:1 as substrate incubated for 30 mins by HTRF assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Key Laboratory Of Structure-Based Drug Design And Discovery (Shenyang Pharmaceutical University)
Curated by ChEMBL
Affinity DataIC50: 529nMAssay Description:Inhibition of EGFR (unknown origin) using poly (Glu, Tyr) 4:1 as substrate incubated for 30 mins by HTRF assayMore data for this Ligand-Target Pair