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Assay Detail

CHEMBL818955

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

Functional
The compound was tested for its effective concentration required to reduce virus plaque formation by using TK (thymidine kinase -deficient) -Varicella-Zoster virus YS/R strain
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Bicyclic nucleoside inhibitors of Varicella-Zoster Virus (VZV): the effect of a terminal halogen substitution in the side-chain.
Brancale A, McGuigan C, Andrei G, Snoeck R, De Clercq E, Balzarini J.
Bioorg Med Chem Lett (2000) 10 : 1215 -1217
PubMed 10866384 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 10 4.83 5.60

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3143184 1 5.60
CHEMBL3143180 1 5.02
CHEMBL3143178 1 4.89
CHEMBL3143183 1 4.64
CHEMBL3143181 1 4.51
CHEMBL3143185 1 4.30
CHEMBL144817 1 -
CHEMBL3143179 1 -
CHEMBL184 ACYCLOVIR 4.0 1 -
CHEMBL3143182 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3143184 EC50 = 2500.0 nM 5.60
CHEMBL3143180 EC50 = 9600.0 nM 5.02
CHEMBL3143178 EC50 = 13000.0 nM 4.89
CHEMBL3143183 EC50 = 23000.0 nM 4.64
CHEMBL3143181 EC50 = 31000.0 nM 4.51
CHEMBL3143185 EC50 = 50000.0 nM 4.30
CHEMBL144817 EC50 > 50000.0 nM -
CHEMBL3143179 EC50 > 20000.0 nM -
CHEMBL184 ACYCLOVIR EC50 = 125000.0 nM -
CHEMBL3143182 EC50 > 50000.0 nM -