null

SMILES CC(=O)Nc1ccc(Nc2cc(c(N)c3C(=O)c4ccccc4C(=O)c23)S([O-])(=O)=O)cc1

InChI Key InChIKey=CKDSSRXGNPFPPZ-UHFFFAOYSA-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 = 50227015   

TargetP2Y purinoceptor 2(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50227015(CHEMBL271688 | Sodium 1-amino-4-(4-acetylaminophen...)copy SMILEScopy InChI
Affinity DataIC50: 5.81E+3nMAssay Description:Antagonist activity at human recombinant P2Y2 receptor in 1321N1 cells assessed as inhibition of UTP-induced calcium mobilizationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9CXTPubMed
TargetP2Y purinoceptor 2(Mus musculus)
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50227015(CHEMBL271688 | Sodium 1-amino-4-(4-acetylaminophen...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Antagonist activity at mouse P2Y2 receptor in mouse NG108-15 cells assessed as inhibition of UTP-induced calcium mobilizationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9CXTPubMed