Compile Data Set for Download or QSAR
Found 289 with Last Name = 'flynn' and Initial = 'r'
TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))TBA
LigandPNGBDBM50605641(CHEMBL5177743)copy SMILES
Affinity DataKi:  0.150nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3J2QPubMed
TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))TBA
LigandPNGBDBM50511467(CHEMBL4551205)copy SMILEScopy InChI
Affinity DataKi:  1.30nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3J2QPubMed
TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))TBA
LigandPNGBDBM50511467(CHEMBL4551205)copy SMILEScopy InChI
Affinity DataKi:  2.10nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35Z0DPubMed
TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))TBA
LigandPNGBDBM50511467(CHEMBL4551205)copy SMILEScopy InChI
Affinity DataKi:  2.70nMAssay Description:Displacement of 6N-FAM from LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence polariz...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35Z0DPubMed
TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))TBA
LigandPNGBDBM50605640(CHEMBL5198453)copy SMILES
Affinity DataKi:  5.30nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3J2QPubMed
TargetRho-associated protein kinase 1(Homo sapiens (Human))TBA
LigandPNGBDBM322158(2-(3-(4-((1H-indazol-5-yl)amino)-6-(4-methylpipera...)copy SMILEScopy InChI
Affinity DataKi:  10nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetRho-associated protein kinase 2(Homo sapiens (Human))TBA
LigandPNGBDBM322152((R)-2-(3-(4-((1H-indazol-5-yl)amino)pyrimidin-2-yl...)copy SMILES
Affinity DataKi:  20nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetRho-associated protein kinase 2(Homo sapiens (Human))TBA
LigandPNGBDBM322158(2-(3-(4-((1H-indazol-5-yl)amino)-6-(4-methylpipera...)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetRho-associated protein kinase 2(Homo sapiens (Human))TBA
LigandPNGBDBM322153(2-(3-(4-((1H-indazol-5-yl)amino)-5-methylpyrimidin...)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetRho-associated protein kinase 1(Homo sapiens (Human))TBA
LigandPNGBDBM448554(US10696660, Y-27263 | US11311541, Example Y-27263)copy SMILEScopy InChI
Affinity DataKi:  40nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetRho-associated protein kinase 2(Homo sapiens (Human))TBA
LigandPNGBDBM322155(US10183931, SLx-2119 | US10696660, SLx-2119 | US11...)copy SMILEScopy InChI
Affinity DataKi:  40nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetRho-associated protein kinase 2(Homo sapiens (Human))TBA
LigandPNGBDBM448554(US10696660, Y-27263 | US11311541, Example Y-27263)copy SMILEScopy InChI
Affinity DataKi:  60nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))TBA
LigandPNGBDBM50511471(CHEMBL4467442)copy SMILEScopy InChI
Affinity DataKi:  64nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35Z0DPubMed
TargetRho-associated protein kinase 1(Homo sapiens (Human))TBA
LigandPNGBDBM322152((R)-2-(3-(4-((1H-indazol-5-yl)amino)pyrimidin-2-yl...)copy SMILES
Affinity DataKi:  70nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetRho-associated protein kinase 2(Homo sapiens (Human))TBA
LigandPNGBDBM322154(2-(3-(4-((1H-indazol-5-yl)amino)-5-methylpyrimidin...)copy SMILEScopy InChI
Affinity DataKi:  80nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))TBA
LigandPNGBDBM50467998(CHEMBL4288877)copy SMILEScopy InChI
Affinity DataKi:  81nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35Z0DPubMed
TargetRho-associated protein kinase 2(Homo sapiens (Human))TBA
LigandPNGBDBM322157(2-(3-(4-((1H-indazol-5-yl)amino)pyrimidin-2-yl)phe...)copy SMILEScopy InChI
Affinity DataKi:  170nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetRho-associated protein kinase 2(Homo sapiens (Human))TBA
LigandPNGBDBM322159((R)-2-(3-(4-((1H-indazol-5-yl)amino)pyrimidin-2-yl...)copy SMILEScopy InChI
Affinity DataKi:  180nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetRho-associated protein kinase 1(Homo sapiens (Human))TBA
LigandPNGBDBM322154(2-(3-(4-((1H-indazol-5-yl)amino)-5-methylpyrimidin...)copy SMILEScopy InChI
Affinity DataKi:  260nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))TBA
LigandPNGBDBM50418303(CHEMBL1765959)copy SMILEScopy InChI
Affinity DataKi:  374nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
TargetSteroidogenic factor 1(Homo sapiens (Human))
Emory University

Curated by ChEMBL
LigandPNGBDBM50511471(CHEMBL4467442)copy SMILEScopy InChI
Affinity DataKi:  418nMAssay Description:Displacement of 6N-FAM from SF1 LBD (218 to 461 residues) (unknown origin) expressed in Escherichia coli BL21 pLysS by competitive binding based fluo...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35Z0DPubMed
TargetRho-associated protein kinase 1(Homo sapiens (Human))TBA
LigandPNGBDBM322155(US10183931, SLx-2119 | US10696660, SLx-2119 | US11...)copy SMILEScopy InChI
Affinity DataKi:  500nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetSteroidogenic factor 1(Homo sapiens (Human))
Emory University

Curated by ChEMBL
LigandPNGBDBM50467998(CHEMBL4288877)copy SMILEScopy InChI
Affinity DataKi:  850nMAssay Description:Displacement of 6N-FAM from SF1 LBD (218 to 461 residues) (unknown origin) expressed in Escherichia coli BL21 pLysS by competitive binding based fluo...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35Z0DPubMed
TargetRho-associated protein kinase 1(Homo sapiens (Human))TBA
LigandPNGBDBM322159((R)-2-(3-(4-((1H-indazol-5-yl)amino)pyrimidin-2-yl...)copy SMILEScopy InChI
Affinity DataKi:  870nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetSteroidogenic factor 1(Homo sapiens (Human))
Emory University

Curated by ChEMBL
LigandPNGBDBM50511467(CHEMBL4551205)copy SMILEScopy InChI
Affinity DataKi:  1.40E+3nMAssay Description:Displacement of 6N-FAM from SF1 LBD (218 to 461 residues) (unknown origin) expressed in Escherichia coli BL21 pLysS by competitive binding based fluo...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35Z0DPubMed
TargetRho-associated protein kinase 1(Homo sapiens (Human))TBA
LigandPNGBDBM322153(2-(3-(4-((1H-indazol-5-yl)amino)-5-methylpyrimidin...)copy SMILEScopy InChI
Affinity DataKi:  2.01E+3nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))TBA
LigandPNGBDBM50511468(CHEMBL4452196)copy SMILEScopy InChI
Affinity DataKi:  2.40E+3nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35Z0DPubMed
TargetSteroidogenic factor 1(Homo sapiens (Human))
Emory University

Curated by ChEMBL
LigandPNGBDBM50418303(CHEMBL1765959)copy SMILEScopy InChI
Affinity DataKi:  3.30E+3nMAssay Description:Displacement of 6N-FAM from SF1 LBD (218 to 461 residues) (unknown origin) expressed in Escherichia coli BL21 pLysS by competitive binding based fluo...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35Z0DPubMed
TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))TBA
LigandPNGBDBM50511470(CHEMBL4448429)copy SMILEScopy InChI
Affinity DataKi:  7.00E+3nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35Z0DPubMed
TargetSteroidogenic factor 1(Homo sapiens (Human))
Emory University

Curated by ChEMBL
LigandPNGBDBM50511468(CHEMBL4452196)copy SMILEScopy InChI
Affinity DataKi:  7.80E+3nMAssay Description:Displacement of 6N-FAM from SF1 LBD (218 to 461 residues) (unknown origin) expressed in Escherichia coli BL21 pLysS by competitive binding based fluo...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35Z0DPubMed
TargetLow molecular weight phosphotyrosine protein phosphatase(Homo sapiens (Human))
Saint John's University

Curated by ChEMBL
LigandPNGBDBM50118216((4-formyl-5-hydroxy-6-methylpyridin-3-yl)methyl di...)copy SMILEScopy InChI
Affinity DataKi:  1.30E+4nMAssay Description:Competitive inhibition of LMW-PTP isoform A (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2MBVPubMed
TargetSteroidogenic factor 1(Homo sapiens (Human))
Emory University

Curated by ChEMBL
LigandPNGBDBM50511470(CHEMBL4448429)copy SMILEScopy InChI
Affinity DataKi:  3.47E+4nMAssay Description:Displacement of 6N-FAM from SF1 LBD (218 to 461 residues) (unknown origin) expressed in Escherichia coli BL21 pLysS by competitive binding based fluo...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35Z0DPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50236362(CHEMBL429743 | N-(4-chlorophenyl)-6-(6,7-dimethoxy...)copy SMILEScopy InChI
Affinity DataIC50: 0.0300nMAssay Description:Inhibition of KDR by HTRF assayMore data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375681(CHEMBL411630)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Inhibition of KDR by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375690(CHEMBL270954)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Inhibition of KDR by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375679(CHEMBL270548)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Inhibition of KDR by HTRF assayMore data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375683(CHEMBL409867)copy SMILEScopy InChI
Affinity DataIC50: 0.600nMAssay Description:Inhibition of KDR by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375688(CHEMBL270058)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of KDR by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375692(CHEMBL272878)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of KDR by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
TargetAngiopoietin-1 receptor(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375682(CHEMBL270057)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of Tie2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375682(CHEMBL270057)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of LckMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375673(CHEMBL270306)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of KDR by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375671(CHEMBL429430)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of KDR by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375682(CHEMBL270057)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of KDR by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375676(CHEMBL272875)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of KDR by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
TargetRho-associated protein kinase 2(Homo sapiens (Human))TBA
LigandPNGBDBM299190(N-(4-(1H-pyrazol-4-yl)phenyl)-2-(5-methoxyisoindol...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetRho-associated protein kinase 2(Homo sapiens (Human))TBA
LigandPNGBDBM299173(N-(2-(5-Methoxyisoindolin-2-yl)pyrimidin-4-yl)-1H-...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Dose response curves for Rho-kinase inhibition were derived from a Invitrogen Z′-LYTE™ Kinase Assay Kit (Invitrogen catalog number PV3793). Pur...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GH9N5NUS Patent
TargetAcetylcholinesterase(Bos taurus (bovine))
University of Iowa

Curated by ChEMBL
LigandPNGBDBM50368271(CHEMBL1204112)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Concentration required to inhibit hydrolytic activity of bovine erythrocyte acetylcholinesterase by 50%More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26D5TK2PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375678(CHEMBL272822)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of KDR by HTRF assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50375692(CHEMBL272878)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of LckMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K79ZWPubMed
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