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TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50080550((2-amino-4,5-dimethylthien-3-yl)-[3-(trifluorometh...)
Affinity DataKd:  0.75nMAssay Description:Allosteric enhancer activity at human adenosine A1 receptor expressed in CHO cell membranes assessed as [3H]NECA affinity constant at 1 uM (Kd = 0.87...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/6/2016
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253928((2-amino-4-((4-(4-(trifluoromethyl)phenyl)piperazi...)
Affinity DataKd:  1.90nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253927(4-(4-((5-amino-4-(4-chlorobenzoyl)thiophen-3-yl)me...)
Affinity DataKd:  1.80nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253926((2-amino-4-((4-(benzo[d][1,3]dioxol-5-yl)piperazin...)
Affinity DataKd:  1.90nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253925((2-amino-4-((4-p-tolylpiperazin-1-yl)methyl)thioph...)
Affinity DataKd:  1.70nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253892((2-amino-4-((4-(4-chlorophenyl)piperazin-1-yl)meth...)
Affinity DataKd:  1.80nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253891((2-amino-4-((4-(4-fluorophenyl)piperazin-1-yl)meth...)
Affinity DataKd:  1.80nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253890((2-amino-4-((4-benzylpiperazin-1-yl)methyl)thiophe...)
Affinity DataKd:  1.70nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253889((2-amino-4-((4-phenylpiperazin-1-yl)methyl)thiophe...)
Affinity DataKd:  1.90nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253888((2-amino-4-((4-cyclohexylpiperazin-1-yl)methyl)thi...)
Affinity DataKd:  1.90nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50080550((2-amino-4,5-dimethylthien-3-yl)-[3-(trifluorometh...)
Affinity DataKd:  1.10nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253852((2-amino-4-((4-methylpiperazin-1-yl)methyl)thiophe...)
Affinity DataKd:  1.20nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253308((2-amino-4-((4-(pyrimidin-2-yl)piperazin-1-yl)meth...)
Affinity DataKd:  1.10nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253307((2-amino-4-((4-(pyridin-2-yl)piperazin-1-yl)methyl...)
Affinity DataKd:  1.70nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253307((2-amino-4-((4-(pyridin-2-yl)piperazin-1-yl)methyl...)
Affinity DataKd:  1.20nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253928((2-amino-4-((4-(4-(trifluoromethyl)phenyl)piperazi...)
Affinity DataKd:  1nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253852((2-amino-4-((4-methylpiperazin-1-yl)methyl)thiophe...)
Affinity DataKd:  1.70nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50024563(CHEMBL3330574)
Affinity DataKd:  0.460nMAssay Description:Allosteric enhancer activity at human adenosine A1 receptor expressed in CHO cell membranes assessed as [3H]NECA affinity constant at 1 uM (Kd = 0.87...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/6/2016
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50080550((2-amino-4,5-dimethylthien-3-yl)-[3-(trifluorometh...)
Affinity DataKd:  1.80nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253888((2-amino-4-((4-cyclohexylpiperazin-1-yl)methyl)thi...)
Affinity DataKd:  1.10nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253889((2-amino-4-((4-phenylpiperazin-1-yl)methyl)thiophe...)
Affinity DataKd:  1nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253890((2-amino-4-((4-benzylpiperazin-1-yl)methyl)thiophe...)
Affinity DataKd:  1.10nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253891((2-amino-4-((4-(4-fluorophenyl)piperazin-1-yl)meth...)
Affinity DataKd:  1nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253892((2-amino-4-((4-(4-chlorophenyl)piperazin-1-yl)meth...)
Affinity DataKd:  1.10nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253925((2-amino-4-((4-p-tolylpiperazin-1-yl)methyl)thioph...)
Affinity DataKd:  1nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253926((2-amino-4-((4-(benzo[d][1,3]dioxol-5-yl)piperazin...)
Affinity DataKd:  1.10nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253927(4-(4-((5-amino-4-(4-chlorobenzoyl)thiophen-3-yl)me...)
Affinity DataKd:  1.10nMAssay Description:Displacement of [3H]CCPA from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAdenosine receptor A1(Human)
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50253308((2-amino-4-((4-(pyrimidin-2-yl)piperazin-1-yl)meth...)
Affinity DataKd:  1.70nMAssay Description:Displacement of [3H]DPCPX from human adenosine A1 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216395(isoquinolinesulfon-5-yl-{2-[4-(2-fluorophenyl)pipe...)
Affinity DataIC50: 12nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216402(N-(2-(4-(4-nitrophenyl)piperazin-1-yl)-2-oxoethyl)...)
Affinity DataIC50: 21nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216390(N-(2-(4-benzylpiperazin-1-yl)-2-oxoethyl)isoquinol...)
Affinity DataIC50: 35nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216397(isoquinolinesulfon-5-yl-{2-[4-(4-acetylphenyl)pipe...)
Affinity DataIC50: 40nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216409(N-(2-oxo-2-(4-phenethylpiperazin-1-yl)ethyl)isoqui...)
Affinity DataIC50: 40nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216388(isoquinolinesulfon-5-yl-{2-[4-(4-fluorophenyl)pipe...)
Affinity DataIC50: 60nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216384(isoquinolinesulfon-5-yl-[2-(4-naphthalen-1-yl-pipe...)
Affinity DataIC50: 90nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216372(isoquinolinesulfon-5-yl-[2-(4-benzylpiperazin-1-yl...)
Affinity DataIC50: 100nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216373(isoquinolinesulfon-5-yl-[2-oxo-2-(4-p-tolylpiperaz...)
Affinity DataIC50: 130nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216377(isoquinolinesulfon-5-yl-[3-oxo-3-(4-phenylpiperazi...)
Affinity DataIC50: 800nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216400(isoquinolinesulfon-5-yl-[2-(4-benzyl[1,4]diazepan-...)
Affinity DataIC50: 900nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216412(isoquinolinesulfon-5-yl-{2-[4-(4-iodophenyl)pipera...)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216380(naphthalenesulfon-1-yl-[2-oxo-2-(4-phenethylpipera...)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216381(isoquinolinesulfon-5-yl-{3-[4-(4-fluorophenyl)pipe...)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216405(isoquinolinesulfon-5-yl-{2-[4-(4-bromophenyl)piper...)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216410(isoquinolinesulfon-5-yl-{2-[4-(4-chlorobenzyl)pipe...)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216376(isoquinolinesulfon-5-yl-{3-[4-(4-nitrophenyl)piper...)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216379(isoquinolinesulfon-5-yl-{2-[4-(4-chlorophenyl)pipe...)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216396(naphthalenesulfon-1-yl-[2-(4-phenylpiperazin-1-yl)...)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216383(naphthalenesulfon-1-yl-{2-[4-(2-fluorophenyl)piper...)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216394(isoquinolinesulfon-5-yl-{2-[4-(2,4-difluorophenyl)...)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Università

Curated by ChEMBL
LigandPNGBDBM50216374(isoquinolinesulfon-5-yl-{2-[4-(2-fluorophenyl)pipe...)
Affinity DataIC50: 1.00E+3nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as effect on intracellular calcium influxMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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