BDBM50454912 CHEMBL147020

SMILES [#6]-[#8]C1([#6]-c2oc(c(-[#6]\[#6]=[#6](\[#6])-[#6])c(=O)c2-[#6](-[#8])=[#6]1\[#6]=[#6]\[#6](-[#6])-[#6])-c1ccc(-[#8])cc1-[#8])[#8]-[#6]

InChI Key InChIKey=UPTALCXGWGDODJ-XYOKQWHBSA-N

Data  2 KI

  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 = 50454912   

TargetAdenosine receptor A3(Homo sapiens (Human))
National Institute Of Diabetes

Curated by ChEMBL
LigandPNGBDBM50454912(CHEMBL147020)
Affinity DataKi:  4.57E+3nMAssay Description:Ability to displace [125I]-AB-MECA binding from adenosine A3 receptor.Checked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
National Institute Of Diabetes

Curated by ChEMBL
LigandPNGBDBM50454912(CHEMBL147020)
Affinity DataKi:  9.12E+3nMAssay Description:Ability to displace [3H]N6-phenylisopropyladenosine binding from adenosine A1 receptor.Checked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed