null

SMILES COc1ccc(C\C(C(=O)c2ccc(OC)cc2)=C(\C([O-])=O)c2ccc3nsnc3c2)cc1

InChI Key InChIKey=YHQZKVIWXDVHOS-ATJXCDBQSA-M

  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 = 50070874   

TargetEndothelin receptor type B(Sus scrofa)
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM50070874(CHEMBL301971 | Sodium; (Z)-2-benzo[1,2,5]thiadiazo...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+3nMAssay Description:In vitro ability to inhibit specific [125I]ET1 binding to porcine kidney (inner medulla) membranes Endothelin B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TM7BM4PubMed
TargetEndothelin-1 receptor(RAT)
Merck KGaA

Curated by ChEMBL
LigandPNGBDBM50070874(CHEMBL301971 | Sodium; (Z)-2-benzo[1,2,5]thiadiazo...)copy SMILEScopy InChI
Affinity DataIC50: 28nMAssay Description:In vitro ability to inhibit specific [125I]ET1 binding to rat aorta membranes Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TM7BM4PubMed