null

SMILES OC[C@H]1O[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)[C@H](O)[C@@H](O)[C@@H]1F

InChI Key InChIKey=NVBJHOWMMXNNQT-JZMIEXBBSA-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 = 50345499   

TargetP2Y purinoceptor 2(Homo sapiens (Human))
NIDDK

Curated by ChEMBL
LigandPNGBDBM50345499(CHEMBL1784293 | P1-(Uridine-5'-)P4-(4'-deoxy-4'-fl...)copy SMILEScopy InChI
Affinity DataEC50:  620nMAssay 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
LigandPNGBDBM50345499(CHEMBL1784293 | P1-(Uridine-5'-)P4-(4'-deoxy-4'-fl...)copy SMILEScopy InChI
Affinity DataEC50:  1.64E+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
LigandPNGBDBM50345499(CHEMBL1784293 | P1-(Uridine-5'-)P4-(4'-deoxy-4'-fl...)copy SMILEScopy InChI
Affinity DataEC50:  220nMAssay Description:Agonist activity at human P2Y4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7NT0PubMed