null

SMILES COc1ccc([C@H]2[C@@H]([C@H](c3ccc(NC(C)C)nc23)c2ccc3OCOc3c2)C(O)=O)c(OCC(C)C)c1

InChI Key InChIKey=JDIFCWUHBJXZLK-HZFUHODCSA-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 = 50141464   

TargetEndothelin-1 receptor(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50141464((5S,6R,7R)-5-Benzo[1,3]dioxol-5-yl-7-(2-isobutoxy-...)copy SMILEScopy InChI
Affinity DataIC50: 0.860nMAssay Description:Inhibitory activity against [125I]-ET-1 binding to human endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0SB4PubMed
TargetEndothelin receptor type B(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50141464((5S,6R,7R)-5-Benzo[1,3]dioxol-5-yl-7-(2-isobutoxy-...)copy SMILEScopy InChI
Affinity DataIC50: 420nMAssay Description:Inhibitory activity against [125I]-ET-1 binding to human endothelin B receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0SB4PubMed