null

SMILES CCn1nnc(n1)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NCc3cccc(F)c3)nc(Cl)nc12

InChI Key InChIKey=CZCUVDQEGPHUNS-MOROJQBDSA-N

  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 2 hits for monomerid = 50266663   

TargetAdenosine receptor A2a(Homo sapiens (Human))
University of Camerino

Curated by ChEMBL
LigandPNGBDBM50266663(CHEMBL4079433)copy SMILEScopy InChI
Affinity DataKi:  242nMAssay Description:Displacement of [3H]NECA from recombinant human adenosine A2A receptor expressed in CHO cell membranes after 3 hrs by microbeta scintillation countin...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CJ8GZXPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
University of Camerino

Curated by ChEMBL
LigandPNGBDBM50266663(CHEMBL4079433)copy SMILEScopy InChI
Affinity DataEC50:  31nMAssay Description:Agonist activity at recombinant human adenosine A2A receptor expressed in CHO cell membranes assessed as stimulation of adenylyl cyclase activity by ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CJ8GZXPubMed