Compile Data Set for Download or QSAR
maximum 50k data
Found 57 of ki for UniProtKB: A0A384MDV9
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM21866(2-phenylamino-9-(4-hydroxybutyl)-6-oxopurine | 9-(...)
Affinity DataKi:  50nMAssay Description:Binding affinity of the compound towards HSV-1 thymidine kinase was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50370388(5IUDR | Allergan 211 | Allergan-211 | Dendrid | He...)
Affinity DataKi:  90nMAssay Description:Binding affinity constant against HSV-1 thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50367489(CHEMBL1269499)
Affinity DataKi:  90nMAssay Description:Compound was evaluated for Kinetic constant for viral thymidine kinase of Herpes simplex virus (HSV) -1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50366681(BRIVUDINE | BVDU | Bridic | Brivox | Brivudin | Br...)
Affinity DataKi:  100nMAssay Description:Binding affinity constant against HSV-1 thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50367488(FIALURIDINE)
Affinity DataKi:  140nMAssay Description:Compound was evaluated for Kinetic constant for viral thymidine kinase of Herpes simplex virus (HSV) -2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50367487(CHEMBL475717)
Affinity DataKi:  180nMAssay Description:Compound was evaluated for Kinetic constant for viral thymidine kinase of Herpes simplex virus (HSV) -1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM1(dT | thymidine)
Affinity DataKi:  200nMAssay Description:Binding affinity constant against HSV-1 thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50422566(CHEMBL2311131)
Affinity DataKi:  210nMAssay Description:Binding affinity constant against HSV-1 thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50135089(C-BVdU | CHEMBL341644)
Affinity DataKi:  220nMAssay Description:Binding affinity constant against HSV-1 thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50367489(CHEMBL1269499)
Affinity DataKi:  440nMAssay Description:Compound was evaluated for Kinetic constant for viral thymidine kinase of Herpes simplex virus (HSV) -2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50367488(FIALURIDINE)
Affinity DataKi:  950nMAssay Description:Compound was evaluated for Kinetic constant for viral thymidine kinase of Herpes simplex virus (HSV) -2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50367487(CHEMBL475717)
Affinity DataKi:  1.40E+3nMAssay Description:Compound was evaluated for Kinetic constant for viral thymidine kinase of Herpes simplex virus (HSV) -1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50027352(1-(4,5-Dihydroxy-tetrahydro-furan-2-yl)-5-methylsu...)
Affinity DataKi:  2.00E+3nMAssay Description:Compound was tested for the binding affinity to thymidine kinase from HSV-1 infected HeLa BuMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM1(dT | thymidine)
Affinity DataKi:  2.00E+3nMAssay Description:Inhibition of HSV-1 thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50282061(1-((2R,4S,5R)-5-Ethynyl-4-hydroxy-tetrahydro-furan...)
Affinity DataKi:  2.00E+3nMAssay Description:Binding affinity of the compound against HSV-1 Thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM21868(2-amino-9-(4-hydroxybutyl)-6,9-dihydro-3H-purin-6-...)
Affinity DataKi:  2.06E+3nMAssay Description:Binding affinity of the compound towards HSV-1 thymidine kinase was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50282067(1-((2R,4S,5S)-4-Hydroxy-5-methoxy-tetrahydro-furan...)
Affinity DataKi:  2.90E+3nMAssay Description:Binding affinity of the compound against HSV-1 Thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50002692((AZT) 1-(4-Azido-5-hydroxymethyl-tetrahydro-furan-...)
Affinity DataKi:  2.90E+3nMAssay Description:Inhibitory affect against rabbit thymus thymidine kinase and represented as molt/4F kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50027352(1-(4,5-Dihydroxy-tetrahydro-furan-2-yl)-5-methylsu...)
Affinity DataKi:  4.10E+3nMAssay Description:Compound was tested for the binding affinity to thymidine kinase from Varicella zoster virus infected human cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50282063(1-[(2R,4S,5S)-4-Hydroxy-5-(3-phenyl-propoxy)-tetra...)
Affinity DataKi:  4.30E+3nMAssay Description:Binding affinity of the compound against HSV-1 Thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50131914(Phosphoric acid mono-[3-aminomethyl-5-(5-methyl-2,...)
Affinity DataKi:  4.70E+3nMAssay Description:In Vitro inhibition of Thymidine Monophosphatase Kinase (TMPKh)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50207303(5-BROMO-2'-DEOXY URIDINE | 5-bromo-1-((2R,4S,5R)-4...)
Affinity DataKi:  5.06E+3nMAssay Description:Binding affinity against HSV-1(KOS) thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50002692((AZT) 1-(4-Azido-5-hydroxymethyl-tetrahydro-furan-...)
Affinity DataKi:  7.00E+3nMAssay Description:Inhibitory affect against rabbit thymus thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50367921(CHEMBL1790740)
Affinity DataKi:  1.20E+4nMAssay Description:Iinhibitory affect against rabbit thymus thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50135091(1-((1R,3S,4S,6S)-4-Hydroxy-5-hydroxymethyl-bicyclo...)
Affinity DataKi:  1.61E+4nMAssay Description:Binding affinity constant against HSV-1 thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50375778(CHEMBL221982)
Affinity DataKi:  2.00E+4nMAssay Description:Inhibition of human cytoplasmic thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50207303(5-BROMO-2'-DEOXY URIDINE | 5-bromo-1-((2R,4S,5R)-4...)
Affinity DataKi:  2.50E+4nMAssay Description:Binding affinity against HSV-2(333) enzyme thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50021777(2-Amino-9-(4-hydroxy-3-hydroxymethyl-but-2-enyl)-1...)
Affinity DataKi:  2.50E+4nMAssay Description:Binding affinity was determined against Herpes simplex virus (HSV) -1 thymidine kinase in vero cell monolayer cultureMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50282072(1-((2R,4S,5S)-4-Hydroxy-5-phenethyloxy-tetrahydro-...)
Affinity DataKi:  2.60E+4nMAssay Description:Binding affinity of the compound against HSV-1 Thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50131916(Phosphoric acid mono-[3-azidomethyl-5-(5-methyl-2,...)
Affinity DataKi:  3.20E+4nMAssay Description:In Vitro inhibition of Thymidine Monophosphatase Kinase (TMPKh)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50131912(Phosphoric acid mono-[3-fluoromethyl-5-(5-methyl-2...)
Affinity DataKi:  4.00E+4nMAssay Description:In Vitro inhibition of Thymidine Monophosphatase Kinase (TMPKh)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50131910(Phosphoric acid mono-[3-hydroxymethyl-5-(5-methyl-...)
Affinity DataKi:  4.35E+4nMAssay Description:In Vitro inhibition of Thymidine Monophosphatase Kinase (TMPKh)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50021776(2-Amino-9-(2-hydroxy-ethoxymethyl)-5,9-dihydro-pur...)
Affinity DataKi:  4.50E+4nMAssay Description:Compound was evaluated for Kinetic constant for viral thymidine kinase of Herpes simplex virus (HSV) -1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50367920(CHEMBL1790742)
Affinity DataKi:  5.40E+4nMAssay Description:Inhibitory affect against rabbit thymus thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50135086((1S,2S,4S,5R)-5-((1E)-2-Bromovinyl)-1-[4-hydroxy-5...)
Affinity DataKi:  6.29E+4nMAssay Description:Binding affinity constant against HSV-1 thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50135087((1S,2S,4S,5R)-5-Bromo-1-[4-hydroxy-5-(hydroxymethy...)
Affinity DataKi:  6.98E+4nMAssay Description:Binding affinity constant against HSV-1 thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50135088((1S,2S,4S,5R)-1-[4-Hydroxy-5-(hydroxymethyl)bicycl...)
Affinity DataKi:  8.58E+4nMAssay Description:Binding affinity constant against HSV-1 thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50131911(1-(4-Aminomethyl-3-hydroxy-5-hydroxymethyl-tetrahy...)
Affinity DataKi:  1.10E+5nMAssay Description:In Vitro inhibition of Thymidine Monophosphatase Kinase (TMPKh)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50027352(1-(4,5-Dihydroxy-tetrahydro-furan-2-yl)-5-methylsu...)
Affinity DataKi:  1.60E+5nMAssay Description:Compound was tested for the binding affinity to thymidine kinase from HeLa mitochondriaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50021776(2-Amino-9-(2-hydroxy-ethoxymethyl)-5,9-dihydro-pur...)
Affinity DataKi:  1.80E+5nMAssay Description:Compound was evaluated for Kinetic constant for viral thymidine kinase of Herpes simplex virus (HSV) -2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50131909(1-((2R,4R,5S)-4-aminomethyl-5-hydroxymethyl-tetrah...)
Affinity DataKi:  2.20E+5nMAssay Description:In Vitro inhibition of Thymidine Monophosphatase Kinase (TMPKh)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50131907(Phosphoric acid mono-[3-aminomethyl-4-hydroxy-5-(5...)
Affinity DataKi:  2.80E+5nMAssay Description:In Vitro inhibition of Thymidine Monophosphatase Kinase (TMPKh)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50027352(1-(4,5-Dihydroxy-tetrahydro-furan-2-yl)-5-methylsu...)
Affinity DataKi: >4.00E+5nMAssay Description:Compound was tested for the binding affinity to thymidine kinase from HeLa cytosolMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50131913(1-(4,5-Bis-hydroxymethyl-tetrahydro-furan-2-yl)-5-...)
Affinity DataKi:  4.20E+5nMAssay Description:In Vitro inhibition of Thymidine Monophosphatase Kinase (TMPKh)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50013115(1-((2R,5S)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl...)
Affinity DataKi:  4.45E+5nMAssay Description:Inhibitory affect against rabbit thymus thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50013111(1-((2R,5S)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl...)
Affinity DataKi:  5.80E+5nMAssay Description:Inhibitory affect against rabbit thymus thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50013114(Benzoic acid 5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-...)
Affinity DataKi:  5.80E+5nMAssay Description:Inhibitory affect against rabbit thymus thymidine kinase and represented as molt/4F kinase in two references.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50013114(Benzoic acid 5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-...)
Affinity DataKi:  5.80E+5nMAssay Description:Inhibitory affect against rabbit thymus thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50013111(1-((2R,5S)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl...)
Affinity DataKi:  6.15E+5nMAssay Description:Inhibitory affect against rabbit thymus thymidine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase, cytosolic(Homo sapiens (Human))
University Of Massachusetts Medical School

Curated by ChEMBL
LigandPNGBDBM50131915(1-(4-Fluoromethyl-5-hydroxymethyl-tetrahydro-furan...)
Affinity DataKi:  9.70E+5nMAssay Description:In Vitro inhibition of Thymidine Monophosphatase Kinase (TMPKh)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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