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

CHEMBL822271

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

Functional
Evaluated for the anti-VZV activity, the concentration of compounds in uM required to reduce VZV OKA Plaque formation after 5 days in HEL cell cultures compared to untreated controls.
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human alphaherpesvirus 3
Cell Type HEL
Confidence 1 — Organism
Curated By Intermediate

Target

Human alphaherpesvirus 3 (CHEMBL613132)
Type ORGANISM
Organism Human alphaherpesvirus 3

Publication

Highly potent and selective inhibition of varicella-zoster virus by bicyclic furopyrimidine nucleosides bearing an aryl side chain.
McGuigan C, Barucki H, Carangio A, Blewett S, Andrei G, Snoeck R, De Clercq E, Balzarini J, Erichsen JT.
J Med Chem (2000) 43 : 4993 -4997
PubMed 11150169 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 12 7.96 9.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL344738 CF1743 1 9.52
CHEMBL147862 1 9.30
CHEMBL146212 1 8.66
CHEMBL31634 BRIVUDINE 2.0 1 8.52
CHEMBL144792 1 8.27
CHEMBL147162 1 8.00
CHEMBL144817 1 7.82
CHEMBL146310 1 7.70
CHEMBL147046 1 7.40
CHEMBL342980 1 7.05
CHEMBL145868 1 7.00
CHEMBL359446 1 6.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL344738 CF1743 EC50 = 0.3 nM 9.52
CHEMBL147862 EC50 = 0.5 nM 9.30
CHEMBL146212 EC50 = 2.2 nM 8.66
CHEMBL31634 BRIVUDINE EC50 = 3.0 nM 8.52
CHEMBL144792 EC50 = 5.4 nM 8.27
CHEMBL147162 EC50 = 10.0 nM 8.00
CHEMBL144817 EC50 = 15.0 nM 7.82
CHEMBL146310 EC50 = 20.0 nM 7.70
CHEMBL147046 EC50 = 40.0 nM 7.40
CHEMBL342980 EC50 = 90.0 nM 7.05
CHEMBL145868 EC50 = 100.0 nM 7.00
CHEMBL359446 EC50 = 500.0 nM 6.30