null

SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NC3C4CCC3CC4)ncnc12

InChI Key InChIKey=ITCAHRKJDUXOHO-WGJBVEHFSA-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 = 50179182   

TargetAdenosine receptor A3(Rattus norvegicus)
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50179182((2R,3R,4S,5R)-2-(6-(bicyclo[2.2.1]heptan-7-ylamino...)copy SMILEScopy InChI
Affinity DataKi:  103nMAssay Description:Binding affinity to rat adenosine A3 receptor in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CZ36QQPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50179182((2R,3R,4S,5R)-2-(6-(bicyclo[2.2.1]heptan-7-ylamino...)copy SMILEScopy InChI
Affinity DataKi:  229nMAssay Description:Binding affinity to human adenosine A3 receptor in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CZ36QQPubMed