BDBM26645 (5Z)-5-[(4-bromophenyl)methylidene]-1,3-thiazolidine-2,4-dione::CHEMBL1946643::thiazolidine-2,4-dione, 23a
SMILES OC1=NC(=O)C(S1)=Cc1ccc(Br)cc1
InChI Key InChIKey=WOJYBXTWFNRUTA-UHFFFAOYSA-N
Data 4 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 26645
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
Medical University of South Carolina
Medical University of South Carolina
Affinity DataIC50: 2.80E+4nMpH: 7.0 T: 2°CAssay Description:The primary screen and evaluation of the compounds was conducted using an ATP-depletion assay. Recombinant human Pim kinase was incubated with S6 kin...More data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Northeast Ohio Medical University
Curated by ChEMBL
Northeast Ohio Medical University
Curated by ChEMBL
Affinity DataIC50: 4.35E+4nMAssay Description:Inhibition of human recombinant MAOA using kynuramine as substrate by fluorimetryMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Northeast Ohio Medical University
Curated by ChEMBL
Northeast Ohio Medical University
Curated by ChEMBL
Affinity DataIC50: 228nMAssay Description:Inhibition of human recombinant MAOB using kynuramine as substrate by fluorimetryMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase pim-2(Homo sapiens (Human))
Medical University of South Carolina
Medical University of South Carolina
Affinity DataIC50: 90nMAssay Description:The primary screen and evaluation of the compounds was conducted using an ATP-depletion assay. Recombinant human Pim kinase was incubated with S6 kin...More data for this Ligand-Target Pair