Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL1111769

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of Varicella zoster virus thymidine kinase assessed as inhibition of [methyl-3H]dThd phosphorylation after 30 mins by scintillation counting
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Human alphaherpesvirus 3
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

3'-[4-Aryl-(1,2,3-triazol-1-yl)]-3'-deoxythymidine analogues as potent and selective inhibitors of human mitochondrial thymidine kinase.
Van Poecke S, Negri A, Gago F, Van Daele I, Solaroli N, Karlsson A, Balzarini J, Van Calenbergh S.
J Med Chem (2010) 53 : 2902 -2912
PubMed 20218622 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 5.29 5.77

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1091988 1 5.77
CHEMBL1090132 1 5.60
CHEMBL1090868 1 5.57
CHEMBL1090134 1 5.51
CHEMBL1091719 1 5.51
CHEMBL1089867 1 5.48
CHEMBL1091931 1 5.43
CHEMBL1089805 1 5.37
CHEMBL1090133 1 5.19
CHEMBL1092729 1 4.82
CHEMBL1090869 1 4.72
CHEMBL1091210 1 4.52
CHEMBL1092055 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1091988 IC50 = 1700.0 nM 5.77
CHEMBL1090132 IC50 = 2500.0 nM 5.60
CHEMBL1090868 IC50 = 2700.0 nM 5.57
CHEMBL1090134 IC50 = 3100.0 nM 5.51
CHEMBL1091719 IC50 = 3100.0 nM 5.51
CHEMBL1089867 IC50 = 3300.0 nM 5.48
CHEMBL1091931 IC50 = 3700.0 nM 5.43
CHEMBL1089805 IC50 = 4300.0 nM 5.37
CHEMBL1090133 IC50 = 6400.0 nM 5.19
CHEMBL1092729 IC50 = 15000.0 nM 4.82
CHEMBL1090869 IC50 = 19000.0 nM 4.72
CHEMBL1091210 IC50 = 30000.0 nM 4.52
CHEMBL1092055 IC50 > 500000.0 nM -