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

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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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
LigandPNGBDBM50393731(CHEMBL2159136)copy SMILEScopy InChI
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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393731(CHEMBL2159136)copy SMILEScopy InChI
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
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed