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Assay Detail

CHEMBL2066972

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

Functional
Antiviral activity against thymidine kinase negative VZV 07/01 infected in HEL cells by plaque formation assay
15
Total Activities
15
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 Autocuration

Target

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

Publication

Synthesis and antiviral activities of hexadecyloxypropyl prodrugs of acyclic nucleoside phosphonates containing guanine or hypoxanthine and a (S)-HPMP or PEE acyclic moiety.
Tichý T, Andrei G, Snoeck R, Balzarini J, Dračínský M, Krečmerová M.
Eur J Med Chem (2012) 55 : 307 -314
PubMed 22858222 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 15 6.41 8.77

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2063192 1 8.77
CHEMBL2063194 1 8.30
CHEMBL419692 1 6.68
CHEMBL2063195 1 6.64
CHEMBL2063188 1 6.52
CHEMBL2063190 1 5.85
CHEMBL31634 BRIVUDINE 2.0 1 4.28
CHEMBL184 ACYCLOVIR 4.0 1 4.27
CHEMBL2063185 1 -
CHEMBL2063186 1 -
CHEMBL2063187 1 -
CHEMBL2063189 1 -
CHEMBL2063193 1 -
CHEMBL182 GANCICLOVIR 4.0 1 -
CHEMBL5314375 CIDOFOVIR 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2063192 EC50 = 1.7 nM 8.77
CHEMBL2063194 EC50 = 5.0 nM 8.30
CHEMBL419692 EC50 = 210.0 nM 6.68
CHEMBL2063195 EC50 = 230.0 nM 6.64
CHEMBL2063188 EC50 = 300.0 nM 6.52
CHEMBL2063190 EC50 = 1400.0 nM 5.85
CHEMBL31634 BRIVUDINE EC50 = 53000.0 nM 4.28
CHEMBL184 ACYCLOVIR EC50 = 54000.0 nM 4.27
CHEMBL2063185 EC50 > 23400.0 nM -
CHEMBL2063186 EC50 > 23000.0 nM -
CHEMBL2063187 EC50 > 35000.0 nM -
CHEMBL2063189 EC50 > 4600.0 nM -
CHEMBL2063193 EC50 > 1400.0 nM -
CHEMBL182 GANCICLOVIR EC50 - -
CHEMBL5314375 CIDOFOVIR EC50 - -