null

SMILES CC(C)(F)c1nc(no1)C12CCC(CN(C(=O)[C@H]3C[C@@](O)(C3)C(F)(F)F)c3cccc(c3)-c3ccc(cc3)C(C)(C)O)(CC1)CC2

InChI Key

PDB links: 1 PDB ID matches this monomer.

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 19 hits for monomerid = 50600733   

TargetBile acid receptor(Mus musculus)TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataEC50:  14nMMore data for this Ligand-Target Pair
TargetRNA-binding protein FXR2(Homo sapiens)TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataEC50: >4.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetRNA-binding protein FXR2(Homo sapiens)TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataEC50:  191nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetRNA-binding protein FXR2(Homo sapiens)TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataEC50:  85nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetRNA-binding protein FXR2(Homo sapiens)TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataEC50:  389nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetNuclear receptor subfamily 1 group I member 2(Homo sapiens (Human))TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataEC50:  5.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataIC50: 5.00E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataIC50: 7.00E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataIC50: 2.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataIC50: 2.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataIC50: 2.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetCytochrome P450 2C8(Homo sapiens (Human))TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataIC50: 2.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataIC50: 8.00E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataIC50: 1.35E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetBile salt export pump(Homo sapiens (Human))TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataIC50: 1.40E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed
TargetUDP-glucuronosyltransferase 1A1(Homo sapiens (Human))TBA
LigandPNGBDBM50600733(CHEMBL5182534)copy SMILES
Affinity DataIC50: 1.50E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7STNPubMed