Compile Data Set for Download or QSAR
Report error Found 84 Enz. Inhib. hit(s) with all data for entry = 50031311
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310923BDBM50310923({6-Methylamino-2-[(pyridin-3-ylmethyl)-amino]-thie...)
Affinity DataIC50: 3.5nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310932BDBM50310932((+/-)-[2-(1-Pyridin-3-yl-ethylamino)-thieno[3,2-d]...)
Affinity DataIC50: 13nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310921BDBM50310921({6-Chloro-2-[(pyridin-3-ylmethyl)-amino]-thieno[3,...)
Affinity DataIC50: 16nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310909BDBM50310909((5-methylthiophen-2-yl)(2-(1-(pyridin-3-yl)ethylam...)
Affinity DataIC50: 17nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310912BDBM50310912((2-(pyridin-3-ylmethylamino)thieno[3,2-d]pyrimidin...)
Affinity DataIC50: 18nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310934BDBM50310934((S)-[2-(1-Pyridin-3-yl-ethylamino)-thieno[3,2-d]py...)
Affinity DataIC50: 18nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310908BDBM50310908((5-methylthiophen-2-yl)(2-(1-(pyridin-2-yl)ethylam...)
Affinity DataIC50: 19nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310924BDBM50310924({6-Ethylamino-2-[(pyridin-3-ylmethyl)-amino]-thien...)
Affinity DataIC50: 19nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310922BDBM50310922({6-Amino-2-[(pyridin-3-ylmethyl)-amino]-thieno[3,2...)
Affinity DataIC50: 32nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310925BDBM50310925({6-dimethylamino-2-[(pyridine-3-ylmethyl)-amino]-t...)
Affinity DataIC50: 39nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310901BDBM50310901((5-methylthiophen-2-yl)(2-(pyridin-2-ylmethylamino...)
Affinity DataIC50: 43nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310912BDBM50310912((2-(pyridin-3-ylmethylamino)thieno[3,2-d]pyrimidin...)
Affinity DataIC50: 51nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310902BDBM50310902((5-methylthiophen-2-yl)(2-(pyridin-3-ylmethylamino...)
Affinity DataIC50: 55nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310921BDBM50310921({6-Chloro-2-[(pyridin-3-ylmethyl)-amino]-thieno[3,...)
Affinity DataIC50: 62nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310903BDBM50310903((5-methylthiophen-2-yl)(2-(pyrimidin-4-ylmethylami...)
Affinity DataIC50: 92nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310909BDBM50310909((5-methylthiophen-2-yl)(2-(1-(pyridin-3-yl)ethylam...)
Affinity DataIC50: 99nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310919BDBM50310919(pyridin-3-yl(2-(pyridin-3-ylmethylamino)thieno[3,2...)
Affinity DataIC50: 109nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310903BDBM50310903((5-methylthiophen-2-yl)(2-(pyrimidin-4-ylmethylami...)
Affinity DataIC50: 116nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310908BDBM50310908((5-methylthiophen-2-yl)(2-(1-(pyridin-2-yl)ethylam...)
Affinity DataIC50: 118nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310927BDBM50310927(2-[(Pyridin-3-ylmethyl)-amino]-thieno[3,2-d]pyrimi...)
Affinity DataIC50: 120nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310897BDBM50310897((2-(ethylamino)thieno[3,2-d]pyrimidin-4-yl)(5-meth...)
Affinity DataIC50: 126nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310913BDBM50310913((2-(pyridin-3-ylmethylamino)thieno[3,2-d]pyrimidin...)
Affinity DataIC50: 148nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310915BDBM50310915((2-(pyridin-3-ylmethylamino)thieno[3,2-d]pyrimidin...)
Affinity DataIC50: 148nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310904BDBM50310904(N-(4-(5-methylthiophene-2-carbonyl)thieno[3,2-d]py...)
Affinity DataIC50: 161nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310914BDBM50310914((2-(pyridin-3-ylmethylamino)thieno[3,2-d]pyrimidin...)
Affinity DataIC50: 176nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310906BDBM50310906((5-methylthiophen-2-yl)(2-(2-(pyridin-3-yl)ethylam...)
Affinity DataIC50: 177nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310901BDBM50310901((5-methylthiophen-2-yl)(2-(pyridin-2-ylmethylamino...)
Affinity DataIC50: 186nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310931BDBM50310931({2-[(Pyridin-3-ylmethyl)-amino]-thieno[3,2-d]pyrim...)
Affinity DataIC50: 189nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310917BDBM50310917((2-(pyridin-3-ylmethylamino)thieno[3,2-d]pyrimidin...)
Affinity DataIC50: 215nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310896BDBM50310896((2-aminothieno[3,2-d]pyrimidin-4-yl)(5-methylthiop...)
Affinity DataIC50: 220nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310929BDBM50310929(2-[(Pyridin-3-ylmethyl)-amino]-thieno[3,2-d]pyrimi...)
Affinity DataIC50: 256nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310904BDBM50310904(N-(4-(5-methylthiophene-2-carbonyl)thieno[3,2-d]py...)
Affinity DataIC50: 287nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310928BDBM50310928(2-[(Pyridin-3-ylmethyl)-amino]-thieno[3,2-d]pyrimi...)
Affinity DataIC50: 309nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310905BDBM50310905((5-methylthiophen-2-yl)(2-(2-(pyridin-2-yl)ethylam...)
Affinity DataIC50: 351nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310913BDBM50310913((2-(pyridin-3-ylmethylamino)thieno[3,2-d]pyrimidin...)
Affinity DataIC50: 405nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310900BDBM50310900((5-methylthiophen-2-yl)(2-(1-phenylethylamino)thie...)
Affinity DataIC50: 414nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310917BDBM50310917((2-(pyridin-3-ylmethylamino)thieno[3,2-d]pyrimidin...)
Affinity DataIC50: 442nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310906BDBM50310906((5-methylthiophen-2-yl)(2-(2-(pyridin-3-yl)ethylam...)
Affinity DataIC50: 450nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310934BDBM50310934((S)-[2-(1-Pyridin-3-yl-ethylamino)-thieno[3,2-d]py...)
Affinity DataIC50: 468nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310911BDBM50310911((5-methylfuran-2-yl)(2-(pyridin-3-ylmethylamino)th...)
Affinity DataIC50: 468nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310910BDBM50310910((5-chlorothiophen-2-yl)(2-(pyridin-3-ylmethylamino...)
Affinity DataIC50: 487nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310926BDBM50310926(2-[(Pyridin-3-ylmethyl)-amino]-thieno[3,2-d]pyrimi...)
Affinity DataIC50: 495nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310916BDBM50310916(phenyl(2-(pyridin-3-ylmethylamino)thieno[3,2-d]pyr...)
Affinity DataIC50: 511nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310930BDBM50310930(2-[(Pyridin-3-ylmethyl)-amino]-thieno[3,2-d]pyrimi...)
Affinity DataIC50: 571nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310918BDBM50310918((4-methoxyphenyl)(2-(pyridin-3-ylmethylamino)thien...)
Affinity DataIC50: 637nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310929BDBM50310929(2-[(Pyridin-3-ylmethyl)-amino]-thieno[3,2-d]pyrimi...)
Affinity DataIC50: 710nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2a(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310914BDBM50310914((2-(pyridin-3-ylmethylamino)thieno[3,2-d]pyrimidin...)
Affinity DataIC50: 732nMAssay Description:Antagonist activity at human adenosine A2A receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310896BDBM50310896((2-aminothieno[3,2-d]pyrimidin-4-yl)(5-methylthiop...)
Affinity DataIC50: 758nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310920BDBM50310920((2-(pyridin-3-ylmethylamino)thieno[3,2-d]pyrimidin...)
Affinity DataIC50: 869nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
TargetAdenosine receptor A2b(Human)
Vernalis (R&D)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50310905BDBM50310905((5-methylthiophen-2-yl)(2-(2-(pyridin-2-yl)ethylam...)
Affinity DataIC50: 944nMAssay Description:Antagonist activity at human adenosine A2B receptor expressed in CHOK1 cells assessed as inhibition of calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2010
Entry Details Article
PubMed
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