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Selectivity interaction (KinomeScan (DiscoverX)) EUB0000167b CAMKK1
Assay data:1 Tested
SummaryRelated BioAssays by Target
Selectivity interaction (KinomeScan (DiscoverX)) EUB0000169b CAMKK1
CAMKK1 DiscoveRx kinase panel
CaMKK1(h) Kinase panel
Inhibition of CAMKK1 (unknown origin) at 1 uM
SummaryPubMed CitationRelated BioAssays by Target
Inhibition of human recombinant CAMKK1 assessed as reduction in substrate phosphorylation at 50 to 500 nM using ATP and Ulight-CKKSRGDYMTMQIG (IRS-1) incubated for 60 min by LANCE detection method
KinomeScan assay: inhibition of CAMKK1
Assay data:108 Tested
CAMKK1(CAK1LGT5) Takeda global kinase panel
Assay data:1 Activity ≤ 1 µM, 1 Tested
SummaryCompounds, activity ≤ 1 µMRelated BioAssays by Target
CaMKK1(h) Eurofins kinase panel
CAMKK1 ProQinase selectivity panel
CAMKK1 (CAMKKA) Kinase screen
CAMKK1 Invitrogen selectivity data (BI)
CaMKK1(h) Eurofins Kinase panel
CaMKK1(h) Millipore kinase panel
CAMKK1 Invitrogen Lab (UK) kinase screen (BI)
CAMKK1 Kinase panel
Inhibition of human CAMKK1 using CAMKKtide as substrate assessed as residual activity by [gamma-33P]-ATP assay relative to control
Assay data:16 Active, 9 Activity ≤ 1 µM, 19 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Inhibition of wild-type human partial length CAMKK1 (R65 to E414 residues) expressed in bacterial expression system assessed as residual binding at 1 uM by Kinomescan method relative to control
Inhibition of wild-type human partial length CAMKK1 (R65 to E414 residues) expressed in bacterial expression system assessed as residual binding level at 1 uM by Kinomescan method relative to control
Assay data:9 Tested
Inhibition of CAMKK1 (unknown origin) assessed as residual activity measured at 1 uM
Assay data:3 Tested
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