BDBM50257636 5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-2,4-diamine::CHEMBL526307

SMILES COc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1I

InChI Key InChIKey=AATPYXMXFBBKFO-UHFFFAOYSA-N

Data  4 KI  13 IC50

  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 17 hits for monomerid = 50257636   

TargetP2X purinoceptor 1(Human)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of P2X1 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetP2X purinoceptor 3(Human)
Gedeon Richter

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 20nMAssay Description:Antagonist activity at human recombinant P2X3 receptor expressed in HEK293-Tet-on cells assessed as alpha,beta-methylene-ATP-stimulated Ca2+ influx b...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetP2X purinoceptor 3(Human)
Gedeon Richter

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 20nMAssay Description:Antagonist activity at human recombinant P2X3 receptor expressed in HEK293-Tet-on cells assessed as alpha,beta-methylene-ATP-stimulated Ca2+ influx b...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetP2X purinoceptor 2(Human)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 79nMAssay Description:Inhibition of P2X2 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetP2X purinoceptor 3(Rat)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 10nMAssay Description:Antagonist activity at rat recombinant P2X3 receptor expressed in CHO cells by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetP2X purinoceptor 5(Human)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of P2X5 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetP2X purinoceptor 4(Human)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of P2X4 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetP2X purinoceptor 3(Rat)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 10nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cells by FLIPRMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetP2X purinoceptor 2(Human)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 39.8nMAssay Description:Antagonist activity at human P2X2/3 receptor expressed in 1321n1c cells by FLIPRMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetP2X purinoceptor 3(Rat)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 10nMAssay Description:Antagonist activity at rat P2X3 receptor expressed in CHO cells by FLIPRMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetP2X purinoceptor 7(Human)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of P2X7 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetP2X purinoceptor 2(Human)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of P2X2 receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetP2X purinoceptor 2(Human)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataIC50: 39.8nMAssay Description:Antagonist activity at human P2X2/3 receptor expressed in 1321n1c cells by FLIPRMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetHistamine H2 receptor(Human)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataKi:  1.00E+8nMAssay Description:Inhibition of histamine H2 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target5-hydroxytryptamine receptor 3A(Human)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataKi:  1.00E+8nMAssay Description:Inhibition of 5HT3 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target5-hydroxytryptamine receptor 2A(Human)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataKi:  1.00E+8nMAssay Description:Inhibition of 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target5-hydroxytryptamine receptor 6(Human)
Roche Palo Alto

Curated by ChEMBL
LigandPNGBDBM50257636(5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-...)
Affinity DataKi:  1.00E+8nMAssay Description:Inhibition of 5HT6 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed