null

SMILES COc1ccc(NC(=O)Nc2nc3nn(cc3c3nc(nn23)-c2ccco2)C(C)(C)C)cc1

InChI Key InChIKey=KFCJVCKIWKNMNB-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 50094686   

TargetAdenosine receptor A3(Homo sapiens (Human))TBA
LigandPNGBDBM50094686(1-(8-tert-Butyl-2-furan-2-yl-8H-pyrazolo[4,3-e][1,...)copy SMILEScopy InChI
Affinity DataKi:  0.800nMAssay Description:Binding affinity to human adenosine A3 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z18GV
TargetAdenosine receptor A3(Homo sapiens (Human))TBA
LigandPNGBDBM50094686(1-(8-tert-Butyl-2-furan-2-yl-8H-pyrazolo[4,3-e][1,...)copy SMILEScopy InChI
Affinity DataKi:  0.800nMAssay Description:Displacement of [3H]-MRE3008-F20 from human adenosine A3 receptor expressed in CHO cells; range 0.63-1.00More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WWTPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))TBA
LigandPNGBDBM50094686(1-(8-tert-Butyl-2-furan-2-yl-8H-pyrazolo[4,3-e][1,...)copy SMILEScopy InChI
Affinity DataKi:  0.800nMAssay Description:Displacement of [3H]NECA from human adenosine A3 receptor expressed in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23FXPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))TBA
LigandPNGBDBM50094686(1-(8-tert-Butyl-2-furan-2-yl-8H-pyrazolo[4,3-e][1,...)copy SMILEScopy InChI
Affinity DataKi:  0.800nMAssay Description:Binding affinity for human adenosine A3 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2183609PubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Universit£ di Padova

Curated by ChEMBL
LigandPNGBDBM50094686(1-(8-tert-Butyl-2-furan-2-yl-8H-pyrazolo[4,3-e][1,...)copy SMILEScopy InChI
Affinity DataKi:  545nMAssay Description:Displacement of [3H]NECA from human adenosine A2A receptor expressed in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N23FXPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Universit£ di Padova

Curated by ChEMBL
LigandPNGBDBM50094686(1-(8-tert-Butyl-2-furan-2-yl-8H-pyrazolo[4,3-e][1,...)copy SMILEScopy InChI
Affinity DataKi:  545nMAssay Description:Displacement of [3H]-SCH- 58261 from human adenosine A2A receptor expressed in CHO cells; range 461-645More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WWTPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))TBA
LigandPNGBDBM50094686(1-(8-tert-Butyl-2-furan-2-yl-8H-pyrazolo[4,3-e][1,...)copy SMILEScopy InChI
Affinity DataKi:  794nMAssay Description:Displacement of [3H]MRE3008-F20 from human adenosine A3 receptor expressed in CHO cells after 120 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP766QPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Università degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50094686(1-(8-tert-Butyl-2-furan-2-yl-8H-pyrazolo[4,3-e][1,...)copy SMILEScopy InChI
Affinity DataKi:  796nMAssay Description:Displacement of [3H]-DPCPX from human adenosine A1 receptor expressed in CHO cells; range 632-1003More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WWTPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
Università degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50094686(1-(8-tert-Butyl-2-furan-2-yl-8H-pyrazolo[4,3-e][1,...)copy SMILEScopy InChI
Affinity DataKi:  1.72E+3nMAssay Description:Displacement of [3H]-DPCPX from Adenosine A2b receptor expressed in CHO cells; range 1531-1920More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WWTPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))TBA
LigandPNGBDBM50094686(1-(8-tert-Butyl-2-furan-2-yl-8H-pyrazolo[4,3-e][1,...)copy SMILEScopy InChI
Affinity DataIC50: 6.80nMAssay Description:Inhibition of cAMP accumulation in CHO cells expressing human adenosine A3 receptor; range 5.1-8.9More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D21WWTPubMed