null

SMILES Cc1ccccc1C(CCC(O)=O)Oc1cc(OCc2ccsc2)ccc1C#N

InChI Key InChIKey=ARDXPWJWTGZJGO-UHFFFAOYSA-N

  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 3 hits for monomerid = 50065518   

TargetEndothelin-1 receptor(RAT)
Rhône-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50065518(4-[2-Cyano-5-(thiophen-3-ylmethoxy)-phenoxy]-4-o-t...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Concentration required to inhibit 50% Et-1 binding to endothelin A receptor in rat A-10 cells.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN94SRPubMed
TargetEndothelin receptor type B(RAT)
Rh£ne-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50065518(4-[2-Cyano-5-(thiophen-3-ylmethoxy)-phenoxy]-4-o-t...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:In vitro inhibition of [125I]ET1 binding to rat cerebellum Endothelin B receptor.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM594WPubMed
TargetEndothelin-1 receptor(RAT)
Rhône-Poulenc Rorer

Curated by ChEMBL
LigandPNGBDBM50065518(4-[2-Cyano-5-(thiophen-3-ylmethoxy)-phenoxy]-4-o-t...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:In vitro inhibition of [125I]ET1 binding to rat A10 cell Endothelin A receptor.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM594WPubMed