null

SMILES O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(=O)OP(O)(=O)Oc2ccccc2)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O

InChI Key InChIKey=XACAXTUDTIBBSW-FMKGYKFTSA-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 = 50270541   

TargetP2Y purinoceptor 2(Homo sapiens (Human))
NIDDK

Curated by ChEMBL
LigandPNGBDBM50270541(CHEMBL474886 | Uridine-5'-phenyl-tetraphosphate)copy SMILEScopy InChI
Affinity DataEC50:  1.89E+3nMAssay Description:Agonist activity at human P2Y2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7NT0PubMed
TargetP2Y purinoceptor 2(Homo sapiens (Human))
NIDDK

Curated by ChEMBL
LigandPNGBDBM50270541(CHEMBL474886 | Uridine-5'-phenyl-tetraphosphate)copy SMILEScopy InChI
Affinity DataEC50:  1.89E+3nMAssay Description:Agonist activity at human P2Y2 receptor expressed in human 1321N1 cells assessed as [3H]inositol phosphate accumulation by scintillation proximity as...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K07569PubMed
TargetP2Y purinoceptor 2(Homo sapiens (Human))
NIDDK

Curated by ChEMBL
LigandPNGBDBM50270541(CHEMBL474886 | Uridine-5'-phenyl-tetraphosphate)copy SMILEScopy InChI
Affinity DataEC50:  2.76E+3nMAssay Description:Agonist activity at human recombinant P2Y2 receptor expressed in human 1321N1 cells assessed as [3H]inositol phosphate production after 30 mins by sc...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7NT0PubMed