null

SMILES CCCc1cc(=O)n([C@@H]2O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]2O)c(=O)[nH]1

InChI Key InChIKey=LNRVNOYVTJQVGH-QCNRFFRDSA-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 3 hits for monomerid = 50199181   

TargetP2Y purinoceptor 6(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50199181(6-propyl-3-beta-D-ribofuranosyl(1H)pyrimidine-2,4-...)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+3nMAssay 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
TargetP2Y purinoceptor 4(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50199181(6-propyl-3-beta-D-ribofuranosyl(1H)pyrimidine-2,4-...)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 2(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50199181(6-propyl-3-beta-D-ribofuranosyl(1H)pyrimidine-2,4-...)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