null

SMILES CC(C)(C)ONc1ccn([C@@H]2O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]2O)c(=O)n1

InChI Key InChIKey=UJSOQUAGCZVHGO-QCNRFFRDSA-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 2 hits for monomerid = 50345483   

TargetP2Y purinoceptor 4(Homo sapiens (Human))
NIDDK

Curated by ChEMBL
LigandPNGBDBM50345483(CHEMBL1784891 | N4-t-Butyloxycytidine-5'-triphosph...)copy SMILEScopy InChI
Affinity DataEC50:  2.11E+3nMAssay Description:Agonist activity at human P2Y4More 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
LigandPNGBDBM50345483(CHEMBL1784891 | N4-t-Butyloxycytidine-5'-triphosph...)copy SMILEScopy InChI
Affinity DataEC50:  1.50E+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