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TargetReceptor-interacting serine/threonine-protein kinase 2(Homo sapiens (Human))
University of Dundee
Curated by ChEMBL
University of Dundee
Curated by ChEMBL
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibition of RIP2 in the presence of 100uM ATPMore data for this Ligand-Target Pair
TargetReceptor-interacting serine/threonine-protein kinase 2(Homo sapiens (Human))
University of Dundee
Curated by ChEMBL
University of Dundee
Curated by ChEMBL
Affinity DataKd: 2.90E+3nMAssay Description:Average Binding Constant for RIPK2; NA=Not Active at 10 uMMore data for this Ligand-Target Pair
TargetReceptor-interacting serine/threonine-protein kinase 2(Homo sapiens (Human))
University of Dundee
Curated by ChEMBL
University of Dundee
Curated by ChEMBL
Affinity DataKd: 1.30E+3nMAssay Description:Binding constant for RIPK2 kinase domainMore data for this Ligand-Target Pair
TargetReceptor-interacting serine/threonine-protein kinase 2(Homo sapiens (Human))
University of Dundee
Curated by ChEMBL
University of Dundee
Curated by ChEMBL
Affinity DataKd: 1.30E+3nMAssay Description:Binding constant for RIPK2 kinase domainMore data for this Ligand-Target Pair
TargetReceptor-interacting serine/threonine-protein kinase 2(Homo sapiens (Human))
University of Dundee
Curated by ChEMBL
University of Dundee
Curated by ChEMBL
Affinity DataKd: 1.30E+3nMAssay Description:Kinase inhibitors are a new class of therapeutics with a propensity to inhibit multiple targets. The biological consequences of multi-kinase activity...More data for this Ligand-Target Pair
TargetReceptor-interacting serine/threonine-protein kinase 2(Homo sapiens (Human))
University of Dundee
Curated by ChEMBL
University of Dundee
Curated by ChEMBL
Affinity DataKd: 1.30E+3nMAssay Description:Binding affinity to RIPK2More data for this Ligand-Target Pair
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