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

CHEMBL894947

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

Binding
Inhibition of VZV thymidine kinase
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Human alphaherpesvirus 3
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Thymidine kinase (CHEMBL4784)
Type SINGLE PROTEIN
Organism Varicella-zoster virus (strain Dumas) (HHV-3) (Human herpesvirus 3)

Publication

Synthesis and antiviral evaluation of 6-(alkyl-heteroaryl)furo[2,3-d]pyrimidin-2(3H)-one nucleosides and analogues with ethynyl, ethenyl, and ethyl spacers at C6 of the furopyrimidine core.
Robins MJ, Nowak I, Rajwanshi VK, Miranda K, Cannon JF, Peterson MA, Andrei G, Snoeck R, De Clercq E, Balzarini J.
J Med Chem (2007) 50 : 3897 -3905
PubMed 17622128 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 4.86 5.54

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL397671 1 5.54
CHEMBL244824 1 5.43
CHEMBL244615 1 5.38
CHEMBL396223 1 4.82
CHEMBL244825 1 4.75
CHEMBL245043 1 4.62
CHEMBL244826 1 4.52
CHEMBL244614 1 4.47
CHEMBL243987 1 4.19
CHEMBL244409 1 -
CHEMBL244194 1 -
CHEMBL243988 1 -
CHEMBL144817 1 -
CHEMBL201494 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL397671 IC50 = 2900.0 nM 5.54
CHEMBL244824 IC50 = 3700.0 nM 5.43
CHEMBL244615 IC50 = 4200.0 nM 5.38
CHEMBL396223 IC50 = 15000.0 nM 4.82
CHEMBL244825 IC50 = 18000.0 nM 4.75
CHEMBL245043 IC50 = 24000.0 nM 4.62
CHEMBL244826 IC50 = 30000.0 nM 4.52
CHEMBL244614 IC50 = 34000.0 nM 4.47
CHEMBL243987 IC50 = 65000.0 nM 4.19
CHEMBL244409 IC50 > 500000.0 nM -
CHEMBL244194 IC50 > 500000.0 nM -
CHEMBL243988 IC50 = 493000.0 nM -
CHEMBL144817 IC50 >= 500000.0 nM -
CHEMBL201494 IC50 = 217000.0 nM -