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Cytotoxicity against human MSC assessed as cell viability after 48 hrs by CCK-8 assay
Assay data:3 Active, 4 Tested
SummaryCompounds, ActivePubMed Citation
Antiproliferative activity against human SK-OV-3 cells assessed as cell viability after 48 hrs by CCK-8 assay
Assay data:4 Active, 4 Activity ≤ 1 µM, 4 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed Citation
Antiproliferative activity against human HepG2 cells assessed as cell viability after 48 hrs by CCK-8 assay
Assay data:4 Active, 3 Activity ≤ 1 µM, 4 Tested
Antiproliferative activity against human A549 cells assessed as cell viability after 48 hrs by CCK-8 assay
Antiproliferative activity against human HL-60 cells assessed as cell viability after 48 hrs by CCK-8 assay
Inhibition of CK2 (unknown origin)
Assay data:33 Active, 18 Activity ≤ 1 µM, 33 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Inhibition of CK2 in human HL-60 cells assessed as increase in cleaved PARP level at 0.1 to 1 uM by Western blot analysis
Assay data:1 Active, 1 Tested
SummaryCompounds, ActivePubMed CitationRelated BioAssays by Target
Inhibition of CK2 in human HL-60 cells assessed as decrease in p-STAT3 level at 0.1 to 1 uM by Western blot analysis
Inhibition of CK2 in human HL-60 cells assessed as decrease in survivin level at 0.1 to 1 uM by Western blot analysis
Inhibition of CK2 in human HL-60 cells assessed as decrease in p-p21 level at 0.1 to 1 uM by Western blot analysis
Inhibition of CK2 in human HL-60 cells assessed as decrease in p-Akt (S129) level at 0.1 to 1 uM by Western blot analysis
Inhibition of CK2 in human HL-60 cells assessed as decrease in p-alpha-catenin level at 0.1 to 1 uM by Western blot analysis
Binding affinity to CK2 (unknown origin) by cellular thermal shift assay
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