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Selectivity interaction (KinomeScan (DiscoverX)) EUB0000178b MAP3K2
Assay data:1 Tested
SummaryRelated BioAssays by Target
Selectivity interaction (KinomeScan (DiscoverX, competition-binding assay)) EUB0000178b MAP3K2
Assay data:1 Active, 1 Activity ≤ 1 µM, 1 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMRelated BioAssays by Target
Selectivity interaction (Enzymatic assay) EUB0000178b MAP3K2
Inhibition of MEKK2 (unknown origin) at 1 uM relative to control
Assay data:2 Tested
SummaryPubMed CitationRelated BioAssays by Target
Inhibition of wild-type human partial length MAP3K2 (S315 to H619 residues) expressed in mammalian expression system assessed as residual binding level at 1 uM by Kinomescan method relative to control
MAP3K2 DiscoveRx kinase panel
MEKK2(h) Kinase panel
Inhibition of MEKK2 (unknown origin) at 1 uM
KinomeScan assay: inhibition of MAP3K2
Assay data:1 Active, 108 Tested
SummaryCompounds, ActiveRelated BioAssays by Target
MEKK2 [MAP3K2(M3K2LGF1)] Takeda global kinase panel
Assay data:1 Activity ≤ 1 µM, 1 Tested
SummaryCompounds, activity ≤ 1 µMRelated BioAssays by Target
MEKK2(h) Eurofins kinase panel
MEKK2 ProQinase selectivity panel
MAP3K2 (MEKK2) Kinase screen
MAP3K2 Invitrogen selectivity data (BI)
MEKK2(h) Eurofins Kinase panel
MEKK2(h) Millipore kinase panel
MAP3K2 Invitrogen Lab (UK) kinase screen (BI)
MEKK2 Kinase panel
Binding affinity to human MAP3K2 by KINOMEscan scanMAX assay
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Binding affinity to human MAP3K2 at 1 uM by KINOMEscan scanMAX assay relative to control
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