null
SMILES CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H]3[C@H]2OC(=Nc2ccc(OC)cc2)N3C)[C@@](C)(C[C@@H](C)C(=O)N[C@H](C)[C@@H](O)[C@]1(C)O)OC
InChI Key InChIKey=WLKGGVSOAWMXIY-IMWLQTJISA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50393731
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb
Curated by ChEMBL
GlaxoSmithKline Research Centre Zagreb
Curated by ChEMBL
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of human recombinant CYP3A4 using 7-BQ as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb
Curated by ChEMBL
GlaxoSmithKline Research Centre Zagreb
Curated by ChEMBL
Affinity DataIC50: 700nMAssay Description:Inhibition of human recombinant CYP3A4 using DEF as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair