Compile Data Set for Download or QSAR
Found 129 with Last Name = 'agarwal' and Initial = 'l'
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071884(4-[2-(3,4-Difluoro-phenyl)-5-phenyl-1H-pyrrol-3-yl...)copy SMILEScopy InChI
Affinity DataIC50: 4.40nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071873(4-[2-(4-Fluoro-phenyl)-5-(4-methanesulfinyl-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of Mitogen-activated protein kinase p38 alphaMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071873(4-[2-(4-Fluoro-phenyl)-5-(4-methanesulfinyl-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 5.10nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071896(4-[2-(4-Fluoro-phenyl)-5-(4-methanesulfinyl-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071903(4-[5-(4-Nitro-phenyl)-2-phenyl-1H-pyrrol-3-yl]-pyr...)copy SMILEScopy InChI
Affinity DataIC50: 6.10nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 11(Homo sapiens (Human))
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071873(4-[2-(4-Fluoro-phenyl)-5-(4-methanesulfinyl-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 8.10nMAssay Description:Inhibition of Mitogen-activated protein kinase p38 betaMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071867(4-[2-(4-Fluoro-phenyl)-5-(4-methanesulfonyl-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibition of Mitogen-activated protein kinase p38 alphaMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071867(4-[2-(4-Fluoro-phenyl)-5-(4-methanesulfonyl-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 9.80nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 11(Homo sapiens (Human))
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071867(4-[2-(4-Fluoro-phenyl)-5-(4-methanesulfonyl-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of Mitogen-activated protein kinase p38 betaMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071915(4-[2-(4-Fluoro-phenyl)-5-phenyl-1H-pyrrol-3-yl]-py...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071910(4-(5-Phenyl-4-pyridin-4-yl-1H-pyrrol-2-yl)-benzoic...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071919(4-(2,5-Diphenyl-1H-pyrrol-3-yl)-pyridine | CHEMBL4...)copy SMILEScopy InChI
Affinity DataIC50: 17nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071911(4-[5-(4-Fluoro-phenyl)-2-phenyl-1H-pyrrol-3-yl]-py...)copy SMILEScopy InChI
Affinity DataIC50: 17nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071912(4-[2-(4-Chloro-phenyl)-5-phenyl-1H-pyrrol-3-yl]-py...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50077960(4-[5-(3,4-Dichloro-phenyl)-2-phenyl-3H-imidazol-4-...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibitory activity against recombinant human RAF proto-oncogene serine/threonine-protein kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81C8DPubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50077961(3-(2-Phenyl-5-pyridin-4-yl-1H-imidazol-4-yl)-pheno...)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Inhibitory activity against recombinant human RAF proto-oncogene serine/threonine-protein kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81C8DPubMed
TargetMitogen-activated protein kinase 11/12/13/14(Homo sapiens (Human))
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071867(4-[2-(4-Fluoro-phenyl)-5-(4-methanesulfonyl-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Inhibition of LPS-induced p38-related TNF alpha release from human monocytesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071906(4-(5-Phenyl-4-pyridin-4-yl-1H-pyrrol-2-yl)-phenyla...)copy SMILEScopy InChI
Affinity DataIC50: 28nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071914(4-[2-(2,4-Difluoro-phenyl)-5-phenyl-1H-pyrrol-3-yl...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50077957(4-[2-Cyclohexyl-5-(4-fluoro-phenyl)-3H-imidazol-4-...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:Inhibition of c-Jun N-terminal kinase 2-alpha 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81C8DPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071891(4-[2-(3-Chloro-phenyl)-5-phenyl-1H-pyrrol-3-yl]-py...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071897(4-[2-(3,4-Dichloro-phenyl)-5-phenyl-1H-pyrrol-3-yl...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071877(4-[5-(2-Fluoro-phenyl)-2-phenyl-1H-pyrrol-3-yl]-py...)copy SMILEScopy InChI
Affinity DataIC50: 34nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071907(2-(4-Chloro-phenyl)-4-(4-fluoro-phenyl)-5-pyridin-...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM13336(4-[4-(4-fluorophenyl)-2-(4-methanesulfinylphenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 39nMAssay Description:Inhibition of Mitogen-activated protein kinase p38 alphaMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071888(4-[5-(3-Fluoro-phenyl)-2-phenyl-1H-pyrrol-3-yl]-py...)copy SMILEScopy InChI
Affinity DataIC50: 42nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071894(4-[2-(4-Fluoro-phenyl)-5-(4-methylsulfanyl-phenyl)...)copy SMILEScopy InChI
Affinity DataIC50: 44nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071892(3-(5-Phenyl-3-pyridin-4-yl-1H-pyrrol-2-yl)-benzoni...)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071917(4-[5-(3-Nitro-phenyl)-2-phenyl-1H-pyrrol-3-yl]-pyr...)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50077974(4-(4-(4-chlorophenyl)-2-phenyl-1H-imidazol-5-yl)py...)copy SMILEScopy InChI
Affinity DataIC50: 56nMAssay Description:Inhibitory activity against recombinant human RAF proto-oncogene serine/threonine-protein kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81C8DPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071913(4-[2-(4-Fluoro-phenyl)-5-(4-methoxy-phenyl)-1H-pyr...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071916(4-[2,5-Bis-(4-fluoro-phenyl)-1H-pyrrol-3-yl]-pyrid...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 11/12/13/14(Homo sapiens (Human))
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071873(4-[2-(4-Fluoro-phenyl)-5-(4-methanesulfinyl-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 65nMAssay Description:Inhibition of c-Jun N-terminal kinase 2-beta 1More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 11(Homo sapiens (Human))
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM13336(4-[4-(4-fluorophenyl)-2-(4-methanesulfinylphenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 78nMAssay Description:Inhibition of Mitogen-activated protein kinase p38 betaMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071885(4-[2-(4-Chloro-phenyl)-5-(4-fluoro-phenyl)-3H-imid...)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50077958(4-[5-(4-Fluoro-phenyl)-2-piperidin-4-yl-3H-imidazo...)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Inhibitory activity against recombinant human RAF proto-oncogene serine/threonine-protein kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81C8DPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071868(4-(4-Fluoro-phenyl)-2-(4-methanesulfinyl-phenyl)-5...)copy SMILEScopy InChI
Affinity DataIC50: 83nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 11/12/13/14(Homo sapiens (Human))
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM13336(4-[4-(4-fluorophenyl)-2-(4-methanesulfinylphenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 83nMAssay Description:Inhibition of LPS-induced p38-related TNF alpha release from human monocytesMore data for this Ligand-Target Pair
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50077964(4-(2-Phenyl-5-pyridin-4-yl-1H-imidazol-4-yl)-benzo...)copy SMILEScopy InChI
Affinity DataIC50: 86nMAssay Description:Inhibitory activity against recombinant human RAF proto-oncogene serine/threonine-protein kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81C8DPubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50237712(4-(4-(3-chlorophenyl)-2-phenyl-1H-imidazol-5-yl)py...)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Inhibitory activity against recombinant human RAF proto-oncogene serine/threonine-protein kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81C8DPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071882(4-(5-Phenyl-4-pyridin-4-yl-1H-pyrrol-2-yl)-N-(2-pi...)copy SMILEScopy InChI
Affinity DataIC50: 97nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50077951(CHEMBL68572 | [4-(2,5-Diphenyl-3H-imidazol-4-yl)-p...)copy SMILEScopy InChI
Affinity DataIC50: 98nMAssay Description:Inhibition of c-Jun N-terminal kinase 2-alpha 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81C8DPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071908(4-[5-(4-Bromo-phenyl)-2-(4-fluoro-phenyl)-1H-pyrro...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50077979(4-[5-(4-Fluoro-phenyl)-2-piperidin-3-yl-3H-imidazo...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibitory activity against recombinant human RAF proto-oncogene serine/threonine-protein kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81C8DPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071886(4-[2-(4-Fluoro-phenyl)-5-(4-methanesulfinyl-phenyl...)copy SMILEScopy InChI
Affinity DataIC50: 114nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071901(4-(5-Phenyl-2-thiophen-2-yl-1H-pyrrol-3-yl)-pyridi...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50077963(4-(2,5-Diphenyl-3H-imidazol-4-yl)-pyridine | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:Inhibition of c-Jun N-terminal kinase 2-alpha 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81C8DPubMed
TargetMitogen-activated protein kinase 14(Rattus norvegicus)
Merck Research Laboratory

Curated by ChEMBL
LigandPNGBDBM50071905(4-(5-Phenyl-4-pyridin-4-yl-1H-pyrrol-2-yl)-benzoic...)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:Inhibitory potency evaluated against rat p38 kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27D2T9NPubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50077957(4-[2-Cyclohexyl-5-(4-fluoro-phenyl)-3H-imidazol-4-...)copy SMILEScopy InChI
Affinity DataIC50: 135nMAssay Description:Inhibitory activity against recombinant human RAF proto-oncogene serine/threonine-protein kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81C8DPubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50077979(4-[5-(4-Fluoro-phenyl)-2-piperidin-3-yl-3H-imidazo...)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of c-Jun N-terminal kinase 2-alpha 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81C8DPubMed
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