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Inhibition of N-terminal GST-tagged human recombinant Mcl-1 expressed in Escherichia coli /human Bim measured for 60 mins by by TR-FRET based LanthaScreen Eu-Kinase binding assay
Assay data:26 Active, 17 Activity ≤ 1 µM, 29 Tested
SummaryRelated BioAssays by Target
Inhibition of his-tagged human recombinant Bcl-2 expressed in Escherichia coli /human Bim measured for 60 mins by by TR-FRET based LanthaScreen Eu-Kinase binding assay
Assay data:29 Active, 28 Activity ≤ 1 µM, 29 Tested
Inhibition of Bfl-1/Bim (unknown origin) incubated for 30 mins by TR-FRET assay
Assay data:2 Active, 2 Tested
Inhibition of Bfl-1/Bim (unknown origin) assessed as inhibition constant by fluorescence polarization assay
Assay data:2 Active, 1 Activity ≤ 1 µM, 2 Tested
Inhibition of Bfl-1/Bim (unknown origin) by fluorescence polarization assay
AlphaLISA Assay from US Patent US11667652: "MCL1 inhibitors"
Assay data:204 Active, 193 Activity ≤ 1 nM, 204 Activity ≤ 1 µM, 204 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMRelated BioAssays by Target
AlphaLISA assay from US Patent US11643400: "MCL-1 inhibitors"
Assay data:443 Active, 402 Activity ≤ 1 nM, 443 Activity ≤ 1 µM, 443 Tested
Inhibition of Mcl-1/Bim (unknown origin) by fluorescence polarisation assay
Assay data:1 Active, 1 Tested
SummaryCompounds, ActivePubMed CitationRelated BioAssays by Target
Inhibition of Bcl-xL/Bim (unknown origin) by ELISA method
Assay data:2 Active, 3 Tested
Inhibition of GST-tagged Mcl-1/Bim (unknown origin) incubated for 15 mins followed by Bim addition measured after 2 hrs by ELISA method
Assay data:3 Active, 2 Activity ≤ 1 µM, 3 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Inhibition of GST-tagged Bcl-xL/Bim (unknown origin) incubated for 15 mins followed by Bim addition measured after 2 hrs by ELISA method
Inhibition of Bcl-2/Bim (unknown origin) by ELISA method
Assay data:4 Active, 2 Activity ≤ 1 µM, 4 Tested
Inhibition of Mcl-1/Bim (unknown origin) by ELISA method
Assay data:6 Active, 3 Activity ≤ 1 µM, 7 Tested
Binding affinity to Bcl-xL/Bim (unknown origin) assessed as inhibition constant by fluorescence polarization assay
Assay data:6 Active, 5 Activity ≤ 1 µM, 6 Tested
Binding affinity to GST-tagged Bcl-xL/5-FAM-tagged Bim (unknown origin) assessed as inhibition constant by fluorescence polarization assay
Inhibition of C-terminal His6-tagged recombinant human MCL-1 (171 to 327 residues/biotinylated Bim (51 to 76 residues) interaction incubated for 1 hrs followed by Bim addition and measured after 2 hrs by AlphaLISA assay
Assay data:1 Active, 1 Activity ≤ 1 nM, 1 Activity ≤ 1 µM, 1 Tested
Inhibition of MCL1/Bim interaction in human MCF7 cells assessed as disruption of MCL1/Bim complex at 10 uM measured after 24 hrs by co-immunoprecipitation based western blot analysis relative to control
Assay data:3 Tested
SummaryPubMed CitationRelated BioAssays by Target
Cell Free Mcl-1: Bim Affinity Assay (Mcl-1 HTRF) from US Patent US11364248: "Compounds that inhibit Mcl-1 protein"
Assay data:54 Active, 42 Activity ≤ 1 nM, 54 Activity ≤ 1 µM, 54 Tested
Cell Free Mcl-1:Bim Affinity Assay (Mcl-1 HTRF) from US Patent US11279712: "Macrocyclic compounds that inhibit MCL-1 protein"
Assay data:61 Active, 52 Activity ≤ 1 nM, 61 Activity ≤ 1 µM, 61 Tested
Bim Binding Assays (Mcl-1 TR-FRET Assays (with 5% human serum) ) from US Patent US11274105: "Alpha-hydroxy phenylacetic acid pharmacophore or bioisostere Mcl-1 protein antagonists"
Assay data:170 Active, 2 Activity ≤ 1 nM, 158 Activity ≤ 1 µM, 171 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMRelated BioAssays by DepositorRelated BioAssays by Target
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