null

SMILES O[C@H]1[C@@H](O)[C@@H](O[C@@H]1COP(O)(O)=O)n1ccc(=O)n(CC(=O)c2ccccc2)c1=O

InChI Key InChIKey=BVOHBCXZDSIVFU-DTZQCDIJSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50199174   

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

Curated by ChEMBL
LigandPNGBDBM50199174(3-phenacyl-1-beta-D-ribofuranosylpyrimidine-2,4-di...)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist activity at human P2Y2 receptor expressed in 1321N1 cells assessed as IP accumulation by SPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SN09RWPubMed
TargetP2Y purinoceptor 4(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50199174(3-phenacyl-1-beta-D-ribofuranosylpyrimidine-2,4-di...)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist activity at human P2Y4 receptor expressed in 1321N1 cells assessed as IP accumulation by SPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SN09RWPubMed
TargetP2Y purinoceptor 6(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50199174(3-phenacyl-1-beta-D-ribofuranosylpyrimidine-2,4-di...)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist activity at human P2Y6 receptor expressed in 1321N1 cells assessed as IP accumulation by SPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SN09RWPubMed