null

SMILES CCCOc1cc(OC)ccc1[C@H]1[C@@H]([C@H](c2ccc(NC(C)C)nc12)c1ccc2OCOc2c1)C(O)=O

InChI Key InChIKey=YPBPZJHPGUUGME-GMQQYTKMSA-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 = 50141462   

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

Curated by ChEMBL
LigandPNGBDBM50141462((5S,6R,7R)-5-Benzo[1,3]dioxol-5-yl-2-isopropylamin...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay 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
TargetEndothelin-1 receptor(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50141462((5S,6R,7R)-5-Benzo[1,3]dioxol-5-yl-2-isopropylamin...)copy SMILEScopy InChI
Affinity DataIC50: 0.410nMAssay 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