Compile Data Set for Download or QSAR
Found 14 Enz. Inhib. hit(s) with Target = 'Adenosine receptor A2b' and Ligand = 'BDBM50229885'
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataKi:  5.5nMAssay Description:Displacement of [3H]MRE2029-F20 from human recombinant adenosine A2B receptor expressed in HEK293 cells after 120 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2862GXTPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataKi:  5.5nMAssay Description:Binding affinity to human adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24J0G1MPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataKi:  5.5nMAssay Description:Displacement of [3H]MRE2029F20 from human adenosine A2B receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38TFDPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataKi:  5.5nMAssay Description:Binding affinity of compound for displacement of [3H]DPCPX binding in HEK293 membranes expressing human A2B adenosine receptorsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22B8ZSMPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataKi:  5.5nMAssay Description:Antagonist activity against human Adenosine A2b receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542N5DPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataKi:  5.5nMAssay Description:Displacement of [3H] DPCPX from human recombinant Adenosine A2B receptor expressed in HEK293 cells after 60 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8VS9PubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataKi:  5.5nMAssay Description:Antagonist activity against human adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K074GGPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataKi:  5.5nMAssay Description:Displacement of [3H]MRE2029-F20 from human recombinant adenosine A2B receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2862GXTPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataKi:  5.5nMAssay Description:Displacement of [3H]DPCPX from human adenosine receptor A2b expressed in HEK293 cell membranesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571F7GPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataKi:  5.5nMAssay Description:Binding affinity of compound for displacement of specific [3H]- DPCPX binding at human A2B receptors expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22B8ZSMPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataIC50: 38nMAssay Description:Inhibitory activity against cAMP production in CHO cells transfected with human A2B adenosine receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22B8ZSMPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataIC50: 38nMAssay Description:Antagonist activity at human recombinant adenosine A2B receptor expressed in CHO cells assessed as inhibition of NECA-induced [3H]cAMP production aft...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2862GXTPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataKd:  1.65nMAssay Description:Binding affinity to human adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24J0G1MPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50229885(CHEMBL260331 | CHEMBL506685 | N-(benzo[d][1,3]diox...)copy SMILEScopy InChI
Affinity DataKd:  1.70nMAssay Description:Binding affinity of [3H]-MRE 2029-F20 towards human adenosine A2b receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8SBNPubMed