BDBM50036133 7-ethyl-7-hydroxy-(7S)-7,8,11,13-tetrahydro-10H-[1,3]dioxolo[4,5-g]pyrano[3',4':6,7]indolizino[1,2-b]quinoline-8,11-dione::7-ethyl-7-hydroxy-(7S)-7,8,11,13-tetrahydro-10H-[1,3]dioxolo[5,4-g]pyrano[3'',4'':6,7]indolizino[1,2-b]quinoline-8,11-dione::CHEMBL307794
SMILES CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cc5OCOc5cc4cc3Cn1c2=O
InChI Key InChIKey=RPFYDENHBPRCTN-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 5 hits for monomerid = 50036133
Affinity DataIC50: 78nMAssay Description:Inhibition of topoisomerase I activity was determined in vitro by using the cleavable complex assay(calf thymus)More data for this Ligand-Target Pair
Affinity DataEC50: 50nMAssay Description:Effective concentration against DNA topoisomerase IMore data for this Ligand-Target Pair
Affinity DataIC50: 30nMAssay Description:Ability to inhibit calf thymus topoisomerase I when assayed in the cleavable complex formationMore data for this Ligand-Target Pair
Affinity DataIC50: 27nMAssay Description:Inhibition of Topoisomerase I by cleavage complex formation in intact human HL-60 cellsMore data for this Ligand-Target Pair
TargetProbable ATP-dependent RNA helicase DDX5(Homo sapiens)
University of Toledo College of Medicine and Life Sciences
Curated by ChEMBL
University of Toledo College of Medicine and Life Sciences
Curated by ChEMBL
Affinity DataKd: 34nMAssay Description:Binding affinity to human recombinant DDX5 assessed as dissociation constantMore data for this Ligand-Target Pair