BDBM50130916 CHEMBL3632945

SMILES [H][C@@]1(OC1(C)C)[C@@H](O)C[C@](C)(O)C1=C2C[C@H](O)[C@@]3([H])[C@@]4(C)CCC(=O)C(C)(C)[C@]4([H])CC[C@]3(C)[C@@]2(C)CC1=O

InChI Key InChIKey=SSNKUHZPKQIDOG-UHFFFAOYSA-N

Data  1 IC50  1 EC50

  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 = 50130916   

TargetBile acid receptor(Human)
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50130916(CHEMBL3632945)
Affinity DataEC50:  4.07E+4nMAssay Description:Transactivation of FXR (unknown origin) transfected in HepG2 cells co-expressing pBSEP/pGL4.74 incubated for 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/25/2021
Entry Details Article
PubMed
TargetCocaine esterase(Human)
Liaoning University of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50130916(CHEMBL3632945)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human carboxylesterase 2 using 4-benzoyl-N-butyl-1,8-naphthalimide as substrate by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2016
Entry Details Article
PubMed