Compile Data Set for Download or QSAR
maximum 50k data
Found 25 of ki for UniProtKB: P32320
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50065262(1-((3R,4S)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydr...)
Affinity DataKi:  0.00120nMAssay Description:Compound was tested for its binding affinity against cytidine deaminase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50367034(CHEMBL610997)
Affinity DataKi:  25nMAssay Description:Binding affinity for human cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50367034(CHEMBL610997)
Affinity DataKi:  25nMAssay Description:Binding affinity against cytidine deaminase of human liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50391219(CHEMBL2093931)
Affinity DataKi:  40nMAssay Description:Cytidine Deaminase Inhibition in human liverChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50391219(CHEMBL2093931)
Affinity DataKi:  40nMAssay Description:Binding affinity against cytidine deaminase of human liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50421666(CHEMBL2311128 | US9040501, 876404)
Affinity DataKi:  100nMAssay Description:Cytidine Deaminase Inhibition in human liverChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50366986(CHEMBL607779)
Affinity DataKi:  400nMAssay Description:Cytidine Deaminase Inhibition in human liverChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50025464(1-(3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-...)
Affinity DataKi:  400nMAssay Description:Binding affinity against cytidine deaminase of human liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50366986(CHEMBL607779)
Affinity DataKi:  400nMAssay Description:Binding affinity for human cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50421666(CHEMBL2311128 | US9040501, 876404)
Affinity DataKi:  400nMAssay Description:Binding affinity for human cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50391219(CHEMBL2093931)
Affinity DataKi:  900nMAssay Description:Cytidine Deaminase Inhibition in human liverChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50367350(CHEMBL603590)
Affinity DataKi:  2.00E+3nMAssay Description:Binding affinity for human cytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50065260(1-((3R,4S)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydr...)
Affinity DataKi:  2.30E+3nMAssay Description:Apparent Ki (binding affinity) was calculated for the compound against cytidine deaminase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50366985(CHEMBL608656)
Affinity DataKi:  2.80E+3nMAssay Description:Binding affinity against cytidine deaminase of human liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50366987(CHEMBL608479)
Affinity DataKi:  9.00E+3nMAssay Description:Cytidine Deaminase Inhibition in human liverChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50367036(CHEMBL609349)
Affinity DataKi:  1.50E+4nMAssay Description:Binding affinity against cytidine deaminase of human liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50065260(1-((3R,4S)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydr...)
Affinity DataKi:  3.80E+4nMAssay Description:Compound was tested for its binding affinity against cytidine deaminase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50007037(CHEBI:23774 | CHEMBL3237555)
Affinity DataKi:  4.00E+4nMAssay Description:Inhibition of human cytidine deaminase by spectrophotometricallyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50065261(1-((4R,5S)-4,5-Dihydroxy-3-hydroxymethyl-cyclopent...)
Affinity DataKi:  1.00E+5nMAssay Description:Compound was tested for its binding affinity against cytidine deaminase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50087289(1-beta-D-Arabinofuranosylcytosine | 4-Amino-1-beta...)
Affinity DataKi:  1.90E+5nMAssay Description:Inhibitory constant was measured on cytidine/deoxycytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50367035(CHEMBL608655)
Affinity DataKi:  3.00E+5nMAssay Description:Binding affinity against cytidine deaminase of human liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50007025(TETRAHYDROURIDINE)
Affinity DataKi:  4.40E+5nMAssay Description:Inhibition of human cytidine deaminase by spectrophotometricallyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50007155(4-Amino-1-(3-hydroxy-5-hydroxymethyl-4-methylene-t...)
Affinity DataKi:  1.60E+6nMAssay Description:Inhibitory constant was measured on cytidine/deoxycytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50421893(CHEMBL10128)
Affinity DataKi:  7.69E+6nMAssay Description:Inhibitory constant was measured on cytidine/deoxycytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytidine deaminase(Homo sapiens (Human))
National Cancer Institute-Bethesda

Curated by ChEMBL
LigandPNGBDBM50007156(4-Amino-5-fluoro-1-(4-hydroxy-5-hydroxymethyl-3-me...)
Affinity DataKi:  2.51E+7nMAssay Description:Inhibitory constant was measured on cytidine/deoxycytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed