Compile Data Set for Download or QSAR
Report error Found 40 Enz. Inhib. hit(s) with all data for entry = 50016787
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597191(CHEMBL5195631)
Affinity DataEC50:  71nMAssay Description:Antagonist activity at human wild type A1R expressed in CHO-K1 cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by measur...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50053929(N-(9-chloro-2-(furan-2-yl)-[1,2,4]triazolo[1,5-c]q...)
Affinity DataEC50:  36nMAssay Description:Antagonist activity at human wild type A3R expressed in Flp-In-CHO cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by me...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597191(CHEMBL5195631)
Affinity DataKd:  55nMAssay Description:Binding affinity to NLuc human A1 receptor expressed in HEK293 cells assessed as dissociation constant by NanoBRET assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597191(CHEMBL5195631)
Affinity DataKd:  55nMAssay Description:Binding affinity to NLuc human A3 receptor expressed in HEK293 cells assessed as dissociation constant by NanoBRET assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM21220(CHEMBL464859 | N-Ethylcarboxamidoadenosine | Adeno...)
Affinity DataEC50:  0.117nMAssay Description:Antagonist activity at human wild type A3R expressed in Flp-In-CHO cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by me...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597195(CHEMBL5183118)
Affinity DataEC50:  0.537nMAssay Description:Antagonist activity at human wild type A3R expressed in Flp-In-CHO cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by me...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597194(CHEMBL5197567)
Affinity DataEC50:  0.468nMAssay Description:Antagonist activity at human wild type A3R expressed in Flp-In-CHO cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by me...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597193(CHEMBL5203865)
Affinity DataEC50:  1.10nMAssay Description:Antagonist activity at human wild type A3R expressed in Flp-In-CHO cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by me...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597192(CHEMBL5175347)
Affinity DataEC50:  0.316nMAssay Description:Antagonist activity at human wild type A3R expressed in Flp-In-CHO cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by me...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597191(CHEMBL5195631)
Affinity DataEC50:  16nMAssay Description:Antagonist activity at human wild type A3R expressed in Flp-In-CHO cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by me...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM21220(CHEMBL464859 | N-Ethylcarboxamidoadenosine | Adeno...)
Affinity DataEC50:  1.80nMAssay Description:Antagonist activity at human wild type A1R expressed in CHO-K1 cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by measur...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597190(CHEMBL5185411)
Affinity DataEC50:  7.10nMAssay Description:Antagonist activity at human wild type A1R expressed in CHO-K1 cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by measur...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597192(CHEMBL5175347)
Affinity DataEC50:  0.977nMAssay Description:Antagonist activity at human wild type A1R expressed in CHO-K1 cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by measur...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597193(CHEMBL5203865)
Affinity DataEC50:  2.40nMAssay Description:Antagonist activity at human wild type A1R expressed in CHO-K1 cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by measur...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597194(CHEMBL5197567)
Affinity DataEC50:  1.5nMAssay Description:Antagonist activity at human wild type A1R expressed in CHO-K1 cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by measur...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597190(CHEMBL5185411)
Affinity DataEC50:  0.912nMAssay Description:Antagonist activity at human wild type A3R expressed in Flp-In-CHO cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by me...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50053929(N-(9-chloro-2-(furan-2-yl)-[1,2,4]triazolo[1,5-c]q...)
Affinity DataEC50:  48nMAssay Description:Antagonist activity at human wild type A1R expressed in CHO-K1 cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by measur...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM21173(DPCPX | CHEMBL183 | 8-cyclopentyl-1,3-dipropyl-2,3...)
Affinity DataEC50:  933nMAssay Description:Antagonist activity at human wild type A1R expressed in CHO-K1 cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by measur...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597195(CHEMBL5183118)
Affinity DataEC50:  1.10nMAssay Description:Antagonist activity at human wild type A1R expressed in CHO-K1 cells assessed as inhibition of forskolin/ NECA-stimulated cAMP accumulation by measur...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50053929(N-(9-chloro-2-(furan-2-yl)-[1,2,4]triazolo[1,5-c]q...)
Affinity DataKi:  0.115nMAssay Description:Displacement of CA200645 from NLuc human A3 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM21173(DPCPX | CHEMBL183 | 8-cyclopentyl-1,3-dipropyl-2,3...)
Affinity DataKi:  0.589nMAssay Description:Displacement of CA200645 from NLuc human A1 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597191(CHEMBL5195631)
Affinity DataKi:  11nMAssay Description:Displacement of CA200645 from NLuc human A1 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597191(CHEMBL5195631)
Affinity DataKi:  13nMAssay Description:Displacement of CA200645 from NLuc human A3 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597191(CHEMBL5195631)
Affinity DataKi:  21nMAssay Description:Binding affinity to wild type human A1R in presence of CA200645 by saturation NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597191(CHEMBL5195631)
Affinity DataKi:  24nMAssay Description:Binding affinity to human A1R H251 6.52A mutant in presence of CA200645 by saturation NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597191(CHEMBL5195631)
Affinity DataKi:  27nMAssay Description:Binding affinity to human A1R L250 6.51A mutant in presence of CA200645 by saturation NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597191(CHEMBL5195631)
Affinity DataKi:  46nMAssay Description:Binding affinity to human A1R E172 5.30A mutant in presence of CA200645 by saturation NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50053929(N-(9-chloro-2-(furan-2-yl)-[1,2,4]triazolo[1,5-c]q...)
Affinity DataKi:  51nMAssay Description:Displacement of CA200645 from NLuc human A1 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM21220(CHEMBL464859 | N-Ethylcarboxamidoadenosine | Adeno...)
Affinity DataKi:  89nMAssay Description:Displacement of CA200645 from NLuc human A3 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM21220(CHEMBL464859 | N-Ethylcarboxamidoadenosine | Adeno...)
Affinity DataKi:  204nMAssay Description:Displacement of CA200645 from NLuc human A1 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597195(CHEMBL5183118)
Affinity DataKi:  363nMAssay Description:Displacement of CA200645 from NLuc human A3 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597190(CHEMBL5185411)
Affinity DataKi:  380nMAssay Description:Displacement of CA200645 from NLuc human A3 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597193(CHEMBL5203865)
Affinity DataKi:  1.70E+3nMAssay Description:Displacement of CA200645 from NLuc human A3 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597190(CHEMBL5185411)
Affinity DataKi:  6.76E+3nMAssay Description:Displacement of CA200645 from NLuc human A1 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597192(CHEMBL5175347)
Affinity DataKi: <1.00E+4nMAssay Description:Displacement of CA200645 from NLuc human A3 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A3(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597194(CHEMBL5197567)
Affinity DataKi: <1.00E+4nMAssay Description:Displacement of CA200645 from NLuc human A3 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597193(CHEMBL5203865)
Affinity DataKi: <1.00E+4nMAssay Description:Displacement of CA200645 from NLuc human A1 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597192(CHEMBL5175347)
Affinity DataKi: <1.00E+4nMAssay Description:Displacement of CA200645 from NLuc human A1 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597194(CHEMBL5197567)
Affinity DataKi: <1.00E+4nMAssay Description:Displacement of CA200645 from NLuc human A1 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAdenosine receptor A1(Human)
University of Cambridge

Curated by ChEMBL
LigandPNGBDBM50597195(CHEMBL5183118)
Affinity DataKi: <1.00E+4nMAssay Description:Displacement of CA200645 from NLuc human A1 receptor expressed in HEK293 cells assessed as inhibition constant by NanoBRET binding assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed