Compile Data Set for Download or QSAR
Found 14 with Last Name = 'suemune' and Initial = 'k'
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50081804((Difluoro-{(1R,2S)-2-[2-(6-oxo-1,6-dihydro-purin-9...)copy SMILEScopy InChI
Affinity DataKi:  8.80nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in human erythrocyteMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ107BPubMed
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50081803(CHEMBL94840 | {1,1-Difluoro-2-[(3R,4R)-4-(6-oxo-1,...)copy SMILEScopy InChI
Affinity DataKi:  15nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in human erythrocyteMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ107BPubMed
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50081807(({(1R,2S)-2-[2-(2-Amino-6-oxo-1,6-dihydro-purin-9-...)copy SMILEScopy InChI
Affinity DataKi:  28nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in human erythrocyteMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ107BPubMed
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50214705(5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-1,1-di...)copy SMILEScopy InChI
Affinity DataKi:  53nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in human erythrocyteMore data for this Ligand-Target Pair
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50081803(CHEMBL94840 | {1,1-Difluoro-2-[(3R,4R)-4-(6-oxo-1,...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in Cellulomonas spMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ107BPubMed
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50081806(CHEMBL94920 | {1,1-Difluoro-2-[(3R,4S)-4-(6-oxo-1,...)copy SMILEScopy InChI
Affinity DataIC50: 37nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in Cellulomonas spMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ107BPubMed
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50081804((Difluoro-{(1R,2S)-2-[2-(6-oxo-1,6-dihydro-purin-9...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in Cellulomonas spMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ107BPubMed
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50081803(CHEMBL94840 | {1,1-Difluoro-2-[(3R,4R)-4-(6-oxo-1,...)copy SMILEScopy InChI
Affinity DataIC50: 88nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in human erythrocyteMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ107BPubMed
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50081806(CHEMBL94920 | {1,1-Difluoro-2-[(3R,4S)-4-(6-oxo-1,...)copy SMILEScopy InChI
Affinity DataIC50: 320nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in human erythrocyteMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ107BPubMed
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50081807(({(1R,2S)-2-[2-(2-Amino-6-oxo-1,6-dihydro-purin-9-...)copy SMILEScopy InChI
Affinity DataIC50: 330nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in human erythrocyteMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ107BPubMed
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50081804((Difluoro-{(1R,2S)-2-[2-(6-oxo-1,6-dihydro-purin-9...)copy SMILEScopy InChI
Affinity DataIC50: 340nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in Cellulomonas spMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ107BPubMed
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50214705(5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-1,1-di...)copy SMILEScopy InChI
Affinity DataIC50: 380nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in human erythrocyteMore data for this Ligand-Target Pair
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50081807(({(1R,2S)-2-[2-(2-Amino-6-oxo-1,6-dihydro-purin-9-...)copy SMILEScopy InChI
Affinity DataIC50: 390nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in human erythrocyteMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ107BPubMed
TargetPurine nucleoside phosphorylase(Homo sapiens (Human))
Tokyo University of Pharmacy & Life Science

Curated by ChEMBL
LigandPNGBDBM50214705(5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-1,1-di...)copy SMILEScopy InChI
Affinity DataIC50: 540nMAssay Description:Compound was evaluated for inhibition of PNP-catalyzed inosine phosphorylation in Cellulomonas spMore data for this Ligand-Target Pair