Compile Data Set for Download or QSAR
maximum 50k data
Found 19 Enz. Inhib. hit(s) with all data for entry = 50016878
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174697(3-fluoro-N-[5-(7-methoxy-10,11-dihydro-5-oxa-2,4,1...)
Affinity DataIC50:  320nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174698(4-fluoro-N-[5-(7-methoxy-10,11-dihydro-5-oxa-2,4,1...)
Affinity DataIC50:  330nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174686(1-(1-chloro-5-oxa-2,4,11-triaza-dibenzo[a,d]cycloh...)
Affinity DataIC50:  450nMAssay Description:Inhibitory activity against FLT3 kinase in a HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174689(CHEMBL439512 | N-[5-(7,8-dimethoxy-10,11-dihydro-5...)
Affinity DataIC50:  470nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174692(CHEMBL200525 | N-[5-(7-methoxy-10,11-dihydro-5-oxa...)
Affinity DataIC50:  600nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174701(1-(3-chloro-10,11-dihydro-5-oxa-2,4,11-triaza-dibe...)
Affinity DataIC50:  900nMAssay Description:Inhibitory activity against FLT3 kinase in a HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174690(CHEMBL199547 | N-[5-(8-methoxy-10,11-dihydro-5-oxa...)
Affinity DataIC50:  970nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174691(3-fluoro-N-[5-(8-methoxy-10,11-dihydro-5-oxa-2,4,1...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174694(CHEMBL371937 | N-[5-(7,8-dimethoxy-10,11-dihydro-5...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174700(CHEMBL199950 | N-[5-(7,8-dimethoxy-10,11-dihydro-5...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174695(CHEMBL199476 | N-[5-(10,11-dihydro-5-oxa-2,4,11-tr...)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174699(CHEMBL381661 | N-[5-(9-methoxy-10,11-dihydro-5-oxa...)
Affinity DataIC50:  2.20E+3nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174688(CHEMBL200535 | N-[5-(8-methoxy-10,11-dihydro-5-oxa...)
Affinity DataIC50:  3.50E+3nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174687(CHEMBL202926 | N-[5-(10,11-dihydro-5-oxa-2,4,11-tr...)
Affinity DataIC50:  3.70E+3nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174693(CHEMBL200395 | N-[5-(7-diethylamino-10,11-dihydro-...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174686(1-(1-chloro-5-oxa-2,4,11-triaza-dibenzo[a,d]cycloh...)
Affinity DataIC50:  9.50E+3nMAssay Description:Inhibitory activity against KDRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInsulin receptor(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174686(1-(1-chloro-5-oxa-2,4,11-triaza-dibenzo[a,d]cycloh...)
Affinity DataIC50:  9.50E+3nMAssay Description:Inhibitory activity against IRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174696(CHEMBL371458 | N-[5-(6-methoxy-10,11-dihydro-5-oxa...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibitory activity against Aurora A kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Imclone Systems

Curated by ChEMBL
LigandPNGBDBM50174685(1-(1-chloro-10,11-dihydro-5-oxa-2,4,11-triaza-dibe...)
Affinity DataIC50:  1.37E+4nMAssay Description:Inhibitory activity against FLT3 kinase in a HTRF assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed