Compile Data Set for Download or QSAR
Found 48 with Last Name = 'ohkoshi' and Initial = 'e'
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
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50359852(CHEMBL1928925)copy SMILEScopy InChI
Affinity DataIC50: 950nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed
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
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50359851(CHEMBL1928924)copy SMILEScopy InChI
Affinity DataIC50: 1.82E+3nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed
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
LigandPNGBDBM50421320(CHEMBL2088175)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of MerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
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
LigandPNGBDBM50421321(CHEMBL2088176)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of MerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
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
LigandPNGBDBM50421322(CHEMBL2088178)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of MerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
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
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50359855(CHEMBL1928928)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed
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
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50359848(CHEMBL1928921)copy SMILEScopy InChI
Affinity DataIC50: 5.44E+3nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50359853(CHEMBL1928926)copy SMILEScopy InChI
Affinity DataIC50: 7.04E+3nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed
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
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50359850(CHEMBL1928923)copy SMILEScopy InChI
Affinity DataIC50: 8.09E+3nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50359858(CHEMBL1929082)copy SMILEScopy InChI
Affinity DataIC50: 8.65E+3nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421322(CHEMBL2088178)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AxlMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421320(CHEMBL2088175)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AxlMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
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
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50098937((S)-methyl 2-amino-5-(amino(nitroamino)methyleneam...)copy SMILEScopy InChI
Affinity DataIC50: 1.34E+4nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50359859(CHEMBL1929083)copy SMILEScopy InChI
Affinity DataIC50: 1.77E+4nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50359854(CHEMBL1928927)copy SMILEScopy InChI
Affinity DataIC50: 2.33E+4nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50359849(CHEMBL1928922)copy SMILEScopy InChI
Affinity DataIC50: 2.57E+4nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed
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
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
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
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
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 receptor UFO(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421321(CHEMBL2088176)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of AxlMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetTyrosine-protein kinase receptor TYRO3(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421320(CHEMBL2088175)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of Tyro3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetTyrosine-protein kinase receptor TYRO3(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421321(CHEMBL2088176)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of Tyro3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetTyrosine-protein kinase receptor TYRO3(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421322(CHEMBL2088178)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of Tyro3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50359856(CHEMBL1926708)copy SMILEScopy InChI
Affinity DataIC50: 3.63E+4nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
National Cheng Kung University

Curated by ChEMBL
LigandPNGBDBM50359857(CHEMBL1928929)copy SMILEScopy InChI
Affinity DataIC50: 4.33E+4nMAssay Description:Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse BV2 cells measured after 24 hrs of post-stimulation by Griess reaction me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6SPWPubMed