null

SMILES CCCc1nc2c(C)cc(cc2n1Cc1ccc(cc1)-c1ccccc1C(O)=O)C(=O)NCCc1cccc(OC)c1

InChI Key InChIKey=NCAWYFSYLMNGPT-UHFFFAOYSA-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 = 50363830   

TargetType-2 angiotensin II receptor(Homo sapiens (Human))
Beijing Institute of Technology

Curated by ChEMBL
LigandPNGBDBM50363830(CHEMBL1945007)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT2 receptor after 180 mins by gamma countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K4BPWPubMed
TargetType-1 angiotensin II receptor(Homo sapiens (Human))
Beijing Institute of Technology

Curated by ChEMBL
LigandPNGBDBM50363830(CHEMBL1945007)copy SMILEScopy InChI
Affinity DataIC50: 30.8nMAssay Description:Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT1 receptor after 180 mins by gamma countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K4BPWPubMed