Compile Data Set for Download or QSAR
Found 44 with Last Name = 'rinnová' and Initial = 'm'
TargetMu-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120216(2-Amino-N-[({[1-benzyl-2-(5-isobutyl-4-oxo-imidazo...)copy SMILEScopy InChI
Affinity DataKi:  4nMAssay Description:Binding affinity of the compound towards Opioid receptor mu 1 was determined using ([d-Ala2,MePhe4, Gly5-ol]-enkephalin (DAMGO) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM20079(5-chloro-6-[(2-iminopyrrolidin-1-yl)methyl]-1,2,3,...)copy SMILEScopy InChI
Affinity DataKi:  17nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
TargetMu-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50001465((S)-2-[(S)-2-(2-{2-[(S)-2-Amino-3-(4-hydroxy-pheny...)copy SMILEScopy InChI
Affinity DataKi:  24nMAssay Description:Binding affinity of the compound towards Opioid receptor mu 1 was determined using ([d-Ala2,MePhe4, Gly5-ol]-enkephalin (DAMGO) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120219((S)-2-{[(S)-2-(2-{2-[2-Amino-3-(4-hydroxy-phenyl)-...)copy SMILEScopy InChI
Affinity DataKi:  28nMAssay Description:Binding affinity of the compound towards Opioid receptor mu 1 was determined using ([d-Ala2,MePhe4, Gly5-ol]-enkephalin (DAMGO) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50001465((S)-2-[(S)-2-(2-{2-[(S)-2-Amino-3-(4-hydroxy-pheny...)copy SMILEScopy InChI
Affinity DataKi:  31nMAssay Description:Binding affinity of the compound towards Opioid receptor delta 1 was determined using [d-Ser2, Leu5, Thr6] enkephalin (DSLET) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120217((S)-2-{[(S)-2-(2-{2-[2-Amino-3-(4-hydroxy-phenyl)-...)copy SMILEScopy InChI
Affinity DataKi:  46nMAssay Description:Binding affinity of the compound towards Opioid receptor mu 1 was determined using ([d-Ala2,MePhe4, Gly5-ol]-enkephalin (DAMGO) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120217((S)-2-{[(S)-2-(2-{2-[2-Amino-3-(4-hydroxy-phenyl)-...)copy SMILEScopy InChI
Affinity DataKi:  67nMAssay Description:Binding affinity of the compound towards Opioid receptor delta 1 was determined using [d-Ser2, Leu5, Thr6] enkephalin (DSLET) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120220(2-[1-{3-[2-amino-3-(4-hydroxyphenyl)-(2S)-propanoy...)copy SMILEScopy InChI
Affinity DataKi:  92nMAssay Description:Binding affinity of the compound towards Opioid receptor mu 1 was determined using ([d-Ala2,MePhe4, Gly5-ol]-enkephalin (DAMGO) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120213((S)-2-[(S)-2-(2-{2-[2-Amino-3-(4-hydroxy-phenyl)-p...)copy SMILEScopy InChI
Affinity DataKi:  95nMAssay Description:Binding affinity of the compound towards Opioid receptor delta 1 was determined using [d-Ser2, Leu5, Thr6] enkephalin (DSLET) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120216(2-Amino-N-[({[1-benzyl-2-(5-isobutyl-4-oxo-imidazo...)copy SMILEScopy InChI
Affinity DataKi:  109nMAssay Description:Binding affinity of the compound towards Opioid receptor delta 1 was determined using [d-Ser2, Leu5, Thr6] enkephalin (DSLET) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120218((1S,3S)-2-[2-(3-{2-[(S)-2-Amino-3-(4-hydroxy-pheny...)copy SMILEScopy InChI
Affinity DataKi:  141nMAssay Description:Binding affinity of the compound towards Opioid receptor delta 1 was determined using [d-Ser2, Leu5, Thr6] enkephalin (DSLET) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120213((S)-2-[(S)-2-(2-{2-[2-Amino-3-(4-hydroxy-phenyl)-p...)copy SMILEScopy InChI
Affinity DataKi:  145nMAssay Description:Binding affinity of the compound towards Opioid receptor mu 1 was determined using ([d-Ala2,MePhe4, Gly5-ol]-enkephalin (DAMGO) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120219((S)-2-{[(S)-2-(2-{2-[2-Amino-3-(4-hydroxy-phenyl)-...)copy SMILEScopy InChI
Affinity DataKi:  209nMAssay Description:Binding affinity of the compound towards Opioid receptor delta 1 was determined using [d-Ser2, Leu5, Thr6] enkephalin (DSLET) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120220(2-[1-{3-[2-amino-3-(4-hydroxyphenyl)-(2S)-propanoy...)copy SMILEScopy InChI
Affinity DataKi:  229nMAssay Description:Binding affinity of the compound towards Opioid receptor delta 1 was determined using [d-Ser2, Leu5, Thr6] enkephalin (DSLET) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50310203(8-(5-bromo-3-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydro...)copy SMILEScopy InChI
Affinity DataKi:  236nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50201010(((2R,3aR,4R,6R,6aR)-4-(hydroxymethyl)-6-(5-methyl-...)copy SMILEScopy InChI
Affinity DataKi:  236nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50310202((2-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-...)copy SMILEScopy InChI
Affinity DataKi:  236nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50310201((1-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-...)copy SMILEScopy InChI
Affinity DataKi:  236nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50310200((1-hydroxy-3-(5-methyl-2,4-dioxo-3,4-dihydropyrimi...)copy SMILEScopy InChI
Affinity DataKi:  236nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50310199((1-fluoro-3-(5-methyl-2,4-dioxo-3,4-dihydropyrimid...)copy SMILEScopy InChI
Affinity DataKi:  236nMAssay Description:Inhibition of human recombinant thymidine phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120218((1S,3S)-2-[2-(3-{2-[(S)-2-Amino-3-(4-hydroxy-pheny...)copy SMILEScopy InChI
Affinity DataKi:  236nMAssay Description:Binding affinity of the compound towards Opioid receptor mu 1 was determined using ([d-Ala2,MePhe4, Gly5-ol]-enkephalin (DAMGO) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120215((S)-2-[(S)-2-(2-{2-[4-((S)-4-Hydroxy-benzyl)-5-oxo...)copy SMILEScopy InChI
Affinity DataKi:  547nMAssay Description:Binding affinity of the compound towards Opioid receptor mu 1 was determined using ([d-Ala2,MePhe4, Gly5-ol]-enkephalin (DAMGO) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120213((S)-2-[(S)-2-(2-{2-[2-Amino-3-(4-hydroxy-phenyl)-p...)copy SMILEScopy InChI
Affinity DataKi:  1.37E+3nMAssay Description:Binding affinity of the compound towards Opioid receptor kappa 1 was determined using U69,593 as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120219((S)-2-{[(S)-2-(2-{2-[2-Amino-3-(4-hydroxy-phenyl)-...)copy SMILEScopy InChI
Affinity DataKi:  1.69E+3nMAssay Description:Binding affinity of the compound towards Opioid receptor kappa 1 was determined using U69,593 as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120217((S)-2-{[(S)-2-(2-{2-[2-Amino-3-(4-hydroxy-phenyl)-...)copy SMILEScopy InChI
Affinity DataKi:  2.23E+3nMAssay Description:Binding affinity of the compound towards Opioid receptor kappa 1 was determined using U69,593 as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120214((1S,4S)-2-[3-(2-{2-[(S)-2-Amino-3-(4-hydroxy-pheny...)copy SMILEScopy InChI
Affinity DataKi:  2.56E+3nMAssay Description:Binding affinity of the compound towards Opioid receptor mu 1 was determined using ([d-Ala2,MePhe4, Gly5-ol]-enkephalin (DAMGO) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120216(2-Amino-N-[({[1-benzyl-2-(5-isobutyl-4-oxo-imidazo...)copy SMILEScopy InChI
Affinity DataKi:  2.89E+3nMAssay Description:Binding affinity of the compound towards Opioid receptor kappa 1 was determined using U69,593 as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120220(2-[1-{3-[2-amino-3-(4-hydroxyphenyl)-(2S)-propanoy...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity of the compound towards Opioid receptor kappa 1 was determined using U69,593 as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120215((S)-2-[(S)-2-(2-{2-[4-((S)-4-Hydroxy-benzyl)-5-oxo...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity of the compound towards Opioid receptor kappa 1 was determined using U69,593 as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120214((1S,4S)-2-[3-(2-{2-[(S)-2-Amino-3-(4-hydroxy-pheny...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity of the compound towards Opioid receptor kappa 1 was determined using U69,593 as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120218((1S,3S)-2-[2-(3-{2-[(S)-2-Amino-3-(4-hydroxy-pheny...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity of the compound towards Opioid receptor kappa 1 was determined using U69,593 as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50001465((S)-2-[(S)-2-(2-{2-[(S)-2-Amino-3-(4-hydroxy-pheny...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity of the compound towards Opioid receptor kappa 1 was determined using U69,593 as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120215((S)-2-[(S)-2-(2-{2-[4-((S)-4-Hydroxy-benzyl)-5-oxo...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity of the compound towards Opioid receptor delta 1 was determined using [d-Ser2, Leu5, Thr6] enkephalin (DSLET) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Institute for Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50120214((1S,4S)-2-[3-(2-{2-[(S)-2-Amino-3-(4-hydroxy-pheny...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity of the compound towards Opioid receptor delta 1 was determined using [d-Ser2, Leu5, Thr6] enkephalin (DSLET) as the radioligand.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2862FSMPubMed
TargetThymidine phosphorylase(Rattus norvegicus)
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50378690(CHEMBL597306)copy SMILEScopy InChI
Affinity DataIC50: 11nMAssay Description:Inhibition of thymidine phosphorylase in T cell lymphomas of Sprague-Dawley rat in presence of 100 uM thymidine and 200 uM phosphateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Rattus norvegicus)
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50378691(CHEMBL609919)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibition of thymidine phosphorylase in T cell lymphomas of Sprague-Dawley rat in presence of 100 uM thymidine and 200 uM phosphateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Rattus norvegicus)
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50378689(CHEMBL599563)copy SMILEScopy InChI
Affinity DataIC50: 45nMAssay Description:Inhibition of thymidine phosphorylase in T cell lymphomas of Sprague-Dawley rat in presence of 100 uM thymidine and 200 uM phosphateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Rattus norvegicus)
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50378684(CHEMBL599543)copy SMILEScopy InChI
Affinity DataIC50: 45nMAssay Description:Inhibition of thymidine phosphorylase in T cell lymphomas of Sprague-Dawley rat in presence of 100 uM thymidine and 200 uM phosphateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Rattus norvegicus)
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50378687(CHEMBL598328)copy SMILEScopy InChI
Affinity DataIC50: 190nMAssay Description:Inhibition of thymidine phosphorylase in T cell lymphomas of Sprague-Dawley rat in presence of 100 uM thymidine and 200 uM phosphateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Rattus norvegicus)
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50378688(CHEMBL599562)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of thymidine phosphorylase in T cell lymphomas of Sprague-Dawley rat in presence of 100 uM thymidine and 200 uM phosphateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Rattus norvegicus)
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50378685(CHEMBL599544)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:Inhibition of thymidine phosphorylase in T cell lymphomas of Sprague-Dawley rat in presence of 100 uM thymidine and 200 uM phosphateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Rattus norvegicus)
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50378692(CHEMBL611383)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:Inhibition of thymidine phosphorylase in T cell lymphomas of Sprague-Dawley rat in presence of 100 uM thymidine and 200 uM phosphateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Rattus norvegicus)
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50378686(CHEMBL598327)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of thymidine phosphorylase in T cell lymphomas of Sprague-Dawley rat in presence of 100 uM thymidine and 200 uM phosphateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed
TargetThymidine phosphorylase(Rattus norvegicus)
Academy of Sciences of the Czech Republic

Curated by ChEMBL
LigandPNGBDBM50378683(CHEMBL599132)copy SMILEScopy InChI
Affinity DataIC50: 750nMAssay Description:Inhibition of thymidine phosphorylase in T cell lymphomas of Sprague-Dawley rat in presence of 100 uM thymidine and 200 uM phosphateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930V4KPubMed