null

SMILES CC(=O)N[C@H]1[C@@H](OP(O)(=O)OP(O)(=O)OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)n2ccc(=O)[nH]c2=O)O[C@H](CO)[C@@H](O)[C@@H]1O

InChI Key InChIKey=SMSKYAZAKPGTPK-CFRASDGPSA-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 = 50345494   

TargetP2Y purinoceptor 2(Homo sapiens (Human))
NIDDK

Curated by ChEMBL
LigandPNGBDBM50345494(CHEMBL1784889 | P1-(Uridine-5'-)P4-(2'-deoxy-2'-ac...)copy SMILEScopy InChI
Affinity DataEC50:  1.89E+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
TargetP2Y purinoceptor 6(Homo sapiens (Human))
NIDDK

Curated by ChEMBL
LigandPNGBDBM50345494(CHEMBL1784889 | P1-(Uridine-5'-)P4-(2'-deoxy-2'-ac...)copy SMILEScopy InChI
Affinity DataEC50:  5.46E+3nMAssay Description:Agonist activity at human recombinant P2Y6 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
TargetP2Y purinoceptor 4(Homo sapiens (Human))
NIDDK

Curated by ChEMBL
LigandPNGBDBM50345494(CHEMBL1784889 | P1-(Uridine-5'-)P4-(2'-deoxy-2'-ac...)copy SMILEScopy InChI
Affinity DataEC50:  910nMAssay Description:Agonist activity at human P2Y4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7NT0PubMed