BDBM203874 Mcl-1 inhibitor 10
SMILES Cc1c(c(COc2ccccc2)nn1C)-c1cccc2c(CCCOc3cccc4ccccc34)c([nH]c12)C(O)=O
InChI Key InChIKey=BAQCJHZNIFESNU-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 203874
TargetInduced myeloid leukemia cell differentiation protein Mcl-1(Human)
Hunan Provinc
Curated by ChEMBL
Hunan Provinc
Curated by ChEMBL
Affinity DataIC50: 383nMAssay Description:Inhibition of FAM labelled Bid-BH3 binding to N-terminal GST-tagged human recombinant MCL1 expressed in Escherichia coli BL2(DE3) after 60 mins by TR...More data for this Ligand-Target Pair
TargetInduced myeloid leukemia cell differentiation protein Mcl-1(Human)
Hunan Provinc
Curated by ChEMBL
Hunan Provinc
Curated by ChEMBL
Affinity DataIC50: 383nMAssay Description:Inhibition of MCL-1 (unknown origin) by TR-FRET assayMore data for this Ligand-Target Pair
TargetInduced myeloid leukemia cell differentiation protein Mcl-1(Human)
Hunan Provinc
Curated by ChEMBL
Hunan Provinc
Curated by ChEMBL
Affinity DataEC50: >1.10E+4nMAssay Description:Inhibition of MCL-1 in human MOLP8 cells assessed as increase in caspase 3/7 activationMore data for this Ligand-Target Pair
TargetInduced myeloid leukemia cell differentiation protein Mcl-1 [171-327](Human)
Oncology Innovative Medicines Unit
Oncology Innovative Medicines Unit
Affinity DataKi: 104nM ΔG°: -9.49kcal/mole IC50: 383nMpH: 7.4 T: 2°CAssay Description:Compound IC50 values were assessed following a 10-point, half-log10 dilution schema starting at 10 uM compound concentration. The assay was performed...More data for this Ligand-Target Pair