Compile Data Set for Download or QSAR
Found 152 with Last Name = 'partridge' and Initial = 'km'
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194141(CHEMBL3938686)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human mPGES-1 expressed in 293E cells assessed as reduction in conversion of PGH2 to PGE2 after 1.5 min by LC/MS analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125VMXPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194190(CHEMBL3956184)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of mPGES-1 in human whole blood assessed as reduction in LPS-induced PGE2 production preincubated for 30 mins followed by LPS stimulation ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125VMXPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194190(CHEMBL3956184)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human mPGES-1 expressed in 293E cells assessed as reduction in conversion of PGH2 to PGE2 after 1.5 min by LC/MS analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125VMXPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233277(CHEMBL4085873)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human mPGES1 expressed in HEK293 microsomes assessed as reduction in PGE2 production using PGH2 as substrate after 2.5 mins by LC-MS an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233278(CHEMBL4064335)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human mPGES1 expressed in HEK293 microsomes assessed as reduction in PGE2 production using PGH2 as substrate after 2.5 mins by LC-MS an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233281(CHEMBL4084995)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human mPGES1 expressed in HEK293 microsomes assessed as reduction in PGE2 production using PGH2 as substrate after 2.5 mins by LC-MS an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233283(CHEMBL4102262)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of mPGES1 in human whole blood assessed as reduction in LPS-induced PGE2 production preincubated for 30 mins followed by LPS addition meas...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233285(CHEMBL4101413)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human mPGES1 expressed in HEK293 microsomes assessed as reduction in PGE2 production using PGH2 as substrate after 2.5 mins by LC-MS an...More data for this Ligand-Target Pair
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233283(CHEMBL4102262)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human mPGES1 expressed in HEK293 microsomes assessed as reduction in PGE2 production using PGH2 as substrate after 2.5 mins by LC-MS an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194141(CHEMBL3938686)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of mPGES-1 in human whole blood assessed as reduction in LPS-induced PGE2 production preincubated for 30 mins followed by LPS stimulation ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125VMXPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194138(CHEMBL3928608)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of human mPGES-1 expressed in 293E cells assessed as reduction in conversion of PGH2 to PGE2 after 1.5 min by LC/MS analysisMore data for this Ligand-Target Pair
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194141(CHEMBL3938686)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of mPGES-1 in human A549 cells assessed as reduction in recombinant human interleukin-1 beta-induced PGE2 production preincubated for 30 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125VMXPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233274(CHEMBL4067045)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of human mPGES1 expressed in HEK293 microsomes assessed as reduction in PGE2 production using PGH2 as substrate after 2.5 mins by LC-MS an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233276(CHEMBL4078000)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of human mPGES1 expressed in HEK293 microsomes assessed as reduction in PGE2 production using PGH2 as substrate after 2.5 mins by LC-MS an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233280(CHEMBL4063350)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of human mPGES1 expressed in HEK293 microsomes assessed as reduction in PGE2 production using PGH2 as substrate after 2.5 mins by LC-MS an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233284(CHEMBL4071976)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of human mPGES1 expressed in HEK293 microsomes assessed as reduction in PGE2 production using PGH2 as substrate after 2.5 mins by LC-MS an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194190(CHEMBL3956184)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of mPGES-1 in human A549 cells assessed as reduction in recombinant human interleukin-1 beta-induced PGE2 production preincubated for 30 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125VMXPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194140(CHEMBL3947494)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of human mPGES-1 expressed in 293E cells assessed as reduction in conversion of PGH2 to PGE2 after 1.5 min by LC/MS analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125VMXPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233275(CHEMBL4094518)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of mPGES1 in human whole blood assessed as reduction in LPS-induced PGE2 production preincubated for 30 mins followed by LPS addition meas...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233277(CHEMBL4085873)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of mPGES1 in human whole blood assessed as reduction in LPS-induced PGE2 production preincubated for 30 mins followed by LPS addition meas...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233275(CHEMBL4094518)copy SMILEScopy InChI
Affinity DataIC50: 3.5nMAssay Description:Inhibition of mPGES1 in human A549 cells assessed as reduction in IL-1beta-induced PGE2 production preincubated for 30 mins followed by IL-1beta addi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194137(CHEMBL3922684)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of human mPGES-1 expressed in 293E cells assessed as reduction in conversion of PGH2 to PGE2 after 1.5 min by LC/MS analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125VMXPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233275(CHEMBL4094518)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of human mPGES1 expressed in HEK293 microsomes assessed as reduction in PGE2 production using PGH2 as substrate after 2.5 mins by LC-MS an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194138(CHEMBL3928608)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of mPGES-1 in human A549 cells assessed as reduction in recombinant human interleukin-1 beta-induced PGE2 production preincubated for 30 m...More data for this Ligand-Target Pair
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194140(CHEMBL3947494)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of mPGES-1 in human whole blood assessed as reduction in LPS-induced PGE2 production preincubated for 30 mins followed by LPS stimulation ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125VMXPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233284(CHEMBL4071976)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of mPGES1 in human whole blood assessed as reduction in LPS-induced PGE2 production preincubated for 30 mins followed by LPS addition meas...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588146(1-[3-[[5-[2-[3- (trifluoromethyl)anilino] pyrimidi...)copy SMILES
Affinity DataIC50: 5nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588147(1-[4-[[5-[2-(3- chloroanilino)pyrimidin- 5-yl]-3- ...)copy SMILES
Affinity DataIC50: 5nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588164(1-[3-[[6-[2-(3- chloro-4-fluoro- anilino)pyrimidin...)copy SMILES
Affinity DataIC50: 5nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588166(1-[3-[[6-[2-[3- (trifluoromethoxy) anilino]pyrimid...)copy SMILES
Affinity DataIC50: 5nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588172(1-[3-[[6-[2-[2- (trifluoromethoxy) anilino]pyrimid...)copy SMILES
Affinity DataIC50: 5nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588175((E)-1-[4-[[6-[2-(3- chloroanilino)pyrimidin- 5-yl]...)copy SMILES
Affinity DataIC50: 5nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588169(1-[3-[[6-[2-[(6- methyl-2- pyridyl)amino] pyrimidi...)copy SMILES
Affinity DataIC50: 5.58nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588168(1-[(3S)-3-[[6-[2-[3- (difluoromethoxy) anilino]pyr...)copy SMILES
Affinity DataIC50: 5.60nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194193(CHEMBL3926051)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of human mPGES-1 expressed in 293E cells assessed as reduction in conversion of PGH2 to PGE2 after 1.5 min by LC/MS analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125VMXPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233279(CHEMBL4092750)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of human mPGES1 expressed in HEK293 microsomes assessed as reduction in PGE2 production using PGH2 as substrate after 2.5 mins by LC-MS an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233285(CHEMBL4101413)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of mPGES1 in human whole blood assessed as reduction in LPS-induced PGE2 production preincubated for 30 mins followed by LPS addition meas...More data for this Ligand-Target Pair
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233278(CHEMBL4064335)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of mPGES1 in human whole blood assessed as reduction in LPS-induced PGE2 production preincubated for 30 mins followed by LPS addition meas...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588142(1-[3-[[5-[2-(3- chloroanilino) pyrimidin-5-yl]-3-...)copy SMILES
Affinity DataIC50: 6.01nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588144((S)-1-(3-((5-(2-((3- (difluoromethoxy) phenyl)amin...)copy SMILES
Affinity DataIC50: 6.08nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588173(1-[4-[[6-[2-(3- chlorophenoxy) pyrimidin-5-yl]pyra...)copy SMILES
Affinity DataIC50: 6.11nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588176(1-[4-[[5-[2-(3- chloroanilino)pyrimidin- 5-yl]-3-p...)copy SMILES
Affinity DataIC50: 6.70nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588165(1-[(3S)-3-[[6-[2-[2- (trifluoromethoxy) anilino]py...)copy SMILES
Affinity DataIC50: 6.72nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588161(1-[(2S,3R)-3-[[6- [2-(3- chlorophenoxy) pyrimidin-...)copy SMILES
Affinity DataIC50: 6.88nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588167(1-[4-[[6-[2-[3- (difluoromethoxy) phenoxy]pyrimidi...)copy SMILES
Affinity DataIC50: 6.89nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588124(1-[3-[[5-[2-(3-chloro- 2-fluoro- phenoxy)pyrimidin...)copy SMILES
Affinity DataIC50: 6.89nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))TBA
LigandPNGBDBM588139(1-[3-[[5-[2-(3- chlorophenoxy) pyrimidin-5-yl]-3- ...)copy SMILES
Affinity DataIC50: 6.95nMAssay Description:The BTK and EGFR biochemical assays utilize LANTHASCREENŽ Eu Kinase Binding Assays from Thermo Fisher Scientific, measuring the binding of the kinase...More data for this Ligand-Target Pair
Ligand Info
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38XD6US Patent
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194138(CHEMBL3928608)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of mPGES-1 in human whole blood assessed as reduction in LPS-induced PGE2 production preincubated for 30 mins followed by LPS stimulation ...More data for this Ligand-Target Pair
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50194192(CHEMBL3910746)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of human mPGES-1 expressed in 293E cells assessed as reduction in conversion of PGH2 to PGE2 after 1.5 min by LC/MS analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125VMXPubMed
TargetProstaglandin E synthase(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50233276(CHEMBL4078000)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of mPGES1 in human whole blood assessed as reduction in LPS-induced PGE2 production preincubated for 30 mins followed by LPS addition meas...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P62RZPubMed
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