Compile Data Set for Download or QSAR
Found 26 with Last Name = 'cui' and Initial = 'mt'
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM2579((2S,3R,4R,6R)-3-methoxy-2-methyl-4-(methylamino)-2...)copy SMILEScopy InChI
Affinity DataIC50: 83nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176799(CHEMBL3808617)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176800(CHEMBL3809956)copy SMILEScopy InChI
Affinity DataIC50: 1.08E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176760(CHEMBL3809304)copy SMILEScopy InChI
Affinity DataIC50: 1.14E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176787(CHEMBL3808937)copy SMILEScopy InChI
Affinity DataIC50: 1.24E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176789(CHEMBL3809769)copy SMILEScopy InChI
Affinity DataIC50: 1.72E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176780(CHEMBL3808931)copy SMILEScopy InChI
Affinity DataIC50: 1.84E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176779(CHEMBL3809339)copy SMILEScopy InChI
Affinity DataIC50: 2.01E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176796(CHEMBL3808513)copy SMILEScopy InChI
Affinity DataIC50: 2.06E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176797(CHEMBL3809699)copy SMILEScopy InChI
Affinity DataIC50: 2.25E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176788(CHEMBL3809150)copy SMILEScopy InChI
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176798(CHEMBL3810139)copy SMILEScopy InChI
Affinity DataIC50: 3.43E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176795(CHEMBL3809606)copy SMILEScopy InChI
Affinity DataIC50: 3.56E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176786(CHEMBL3808518)copy SMILEScopy InChI
Affinity DataIC50: 4.17E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50001839(CHEMBL428647 | PACLITAXEL | taxol)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176785(CHEMBL3809070)copy SMILEScopy InChI
Affinity DataIC50: 7.27E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176792(CHEMBL3808665)copy SMILEScopy InChI
Affinity DataIC50: 7.84E+3nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176781(CHEMBL3810009)copy SMILEScopy InChI
Affinity DataIC50: 1.02E+4nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50113707(2,6,9-Trisubstitute purine, 2 | 2-(2-hydroxyethyla...)copy SMILEScopy InChI
Affinity DataIC50: 1.13E+4nMAssay Description:Inhibition of N-terminal His-tagged Mer kinase (588 to 855 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) cells measured every mi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176794(CHEMBL3810240)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176791(CHEMBL3810214)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176790(CHEMBL3809359)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176782(CHEMBL3808451)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176783(CHEMBL3809195)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176784(CHEMBL3809906)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50176793(CHEMBL1623086)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of MERTK (unknown origin) using EFPIYDFLPAKKK-CONH2 as substrate and ATP after 180 mins by microfluidic capillary electrophoresis methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B621JPubMed