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Inhibition of human IGF1R using KKKSPGEYVNIEFG as substrate and [gamma-33P]ATP measured after 1 hr
Assay data:48 Active, 5 Activity ≤ 1 nM, 48 Activity ≤ 1 µM, 50 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Inhibition of human ALK using poly[Glu:Tyr] (4:1) as substrate and [gamma-33P]ATP measured after 1 hr
Assay data:50 Active, 37 Activity ≤ 1 nM, 50 Activity ≤ 1 µM, 50 Tested
SANGER: Inhibition of human DEL cell growth in a cell viability assay.
Assay data:73 Active, 3 Activity ≤ 1 nM, 40 Activity ≤ 1 µM, 129 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µM
SANGER: Inhibition of human SF539 cell growth in a cell viability assay.
Assay data:55 Active, 3 Activity ≤ 1 nM, 34 Activity ≤ 1 µM, 137 Tested
SANGER: Inhibition of human SCC-3 cell growth in a cell viability assay.
Assay data:32 Active, 1 Activity ≤ 1 nM, 18 Activity ≤ 1 µM, 77 Tested
Cytotoxicity against mouse BAF3 cells expressing Tel-ALK after 48 hrs by CellTiter-Glo assay
Assay data:23 Active, 1 Activity ≤ 1 nM, 15 Activity ≤ 1 µM, 34 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed Citation
Binding constant for PLK4 kinase domain
Assay data:33 Active, 2 Activity ≤ 1 nM, 22 Activity ≤ 1 µM, 72 Tested
Binding constant for ULK1 kinase domain
Assay data:19 Active, 1 Activity ≤ 1 nM, 12 Activity ≤ 1 µM, 72 Tested
Binding constant for ROS1 kinase domain
Assay data:19 Active, 1 Activity ≤ 1 nM, 11 Activity ≤ 1 µM, 72 Tested
Binding constant for BMPR1B kinase domain
Assay data:25 Active, 1 Activity ≤ 1 nM, 15 Activity ≤ 1 µM, 72 Tested
Binding constant for LTK kinase domain
Assay data:29 Active, 1 Activity ≤ 1 nM, 14 Activity ≤ 1 µM, 72 Tested
Binding constant for LRRK2(G2019S) kinase domain
Assay data:25 Active, 2 Activity ≤ 1 nM, 17 Activity ≤ 1 µM, 72 Tested
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