BDBM50513531 CHEMBL4435740
SMILES CCCCC\C=C\C=C\C=N\Nc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1
InChI Key InChIKey=LCYPSICJTNPPEJ-LIJLLEJISA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50513531
TargetAdenosine receptor A1(Homo sapiens (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: 2nMAssay 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
TargetAdenosine receptor A2a(Homo sapiens (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: 18nMAssay 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 A2a(Homo sapiens (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: 10nMAssay 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