BDBM50513547 CHEMBL4471366

SMILES Nc1nc(N\N=C\c2ccc(OCc3ccccc3)c(OCc3ccccc3)c2)nc2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

InChI Key InChIKey=DHSFMYUYIXNXST-QTMKEUKHSA-N

Data  2 KI  1 EC50

  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 = 50513547   

TargetAdenosine receptor A2a(Homo sapiens (Human))
National Engineering Research Center For The Emergency Drug

Curated by ChEMBL
LigandPNGBDBM50513547(CHEMBL4471366)
Affinity DataKi:  1.80nMAssay Description:Displacement of [3H]CGS21680 from human cloned adenosine receptor A2A expressed in HEK-293 cell membrane incubated for 60 mins by microbeta counting ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
National Engineering Research Center For The Emergency Drug

Curated by ChEMBL
LigandPNGBDBM50513547(CHEMBL4471366)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]DPCPX from human cloned adenosine receptor A1 expressed in CHO-K1 cell membranes incubated for 60 mins by microbeta counting meth...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
National Engineering Research Center For The Emergency Drug

Curated by ChEMBL
LigandPNGBDBM50513547(CHEMBL4471366)
Affinity DataEC50:  0.640nMAssay Description:Agonist activity at human adenosine receptor A2A expressed in HEK293 cells assessed as cAMP accumulation incubated for 30 mins by Eu-cAMP tracer-base...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed