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-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50513547
TargetAdenosine receptor A2a(Human)
National Engineering Research Center For The Emergency Drug
Curated by ChEMBL
National Engineering Research Center For The Emergency Drug
Curated by ChEMBL
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
TargetAdenosine receptor A2a(Human)
National Engineering Research Center For The Emergency Drug
Curated by ChEMBL
National Engineering Research Center For The Emergency Drug
Curated by ChEMBL
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
TargetAdenosine receptor A1(Human)
National Engineering Research Center For The Emergency Drug
Curated by ChEMBL
National Engineering Research Center For The Emergency Drug
Curated by ChEMBL
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
