null

SMILES CSc1n(C)nc2nc(NC(=O)Cc3ccc4OCOc4c3)n3nc(nc3c12)-c1ccco1

InChI Key InChIKey=JEUBWTWZNZWFQP-UHFFFAOYSA-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 6 hits for monomerid = 50125931   

TargetAdenosine receptor A2a(Homo sapiens (Human))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50125931(2-Benzo[1,3]dioxol-5-yl-N-(2-furan-2-yl-8-methyl-9...)copy SMILEScopy InChI
Affinity DataKi:  4.10nMAssay Description:Displacement of [3H]- SCH-58261 binding at human Adenosine A2A receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28916KPPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50125931(2-Benzo[1,3]dioxol-5-yl-N-(2-furan-2-yl-8-methyl-9...)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:Displacement of [3H]- DPCPX from human adenosine A2B receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28916KPPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50125931(2-Benzo[1,3]dioxol-5-yl-N-(2-furan-2-yl-8-methyl-9...)copy SMILEScopy InChI
Affinity DataKi:  70nMAssay Description:Displacement of [3H]- DPCPX binding at human Adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28916KPPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50125931(2-Benzo[1,3]dioxol-5-yl-N-(2-furan-2-yl-8-methyl-9...)copy SMILEScopy InChI
Affinity DataKi:  110nMAssay Description:Displacement of [3H]- MRE 308F20 binding from human Adenosine A3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28916KPPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50125931(2-Benzo[1,3]dioxol-5-yl-N-(2-furan-2-yl-8-methyl-9...)copy SMILEScopy InChI
Affinity DataIC50: 21.5nMAssay Description:Antagonist activity as inhibition of cAMP generation after agonist-modulation of human Adenosine A2A receptor with 100 nM NECAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28916KPPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50125931(2-Benzo[1,3]dioxol-5-yl-N-(2-furan-2-yl-8-methyl-9...)copy SMILEScopy InChI
Affinity DataIC50: 466nMAssay Description:Antagonist activity as inhibition of cAMP generation after agonist-modulation of Adenosine A3 receptor with 100 nM CI-IB-MECAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28916KPPubMed