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Assay Detail

CHEMBL903157

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

Binding
Inhibition of VZV-TK catalyzed dThd phosphorylation
4
Total Activities
4
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

Synthesis and antiviral activity of the carbocyclic analogue of the highly potent and selective anti-VZV bicyclo furano pyrimidines.
Migliore MD, Zonta N, McGuigan C, Henson G, Andrei G, Snoeck R, Balzarini J.
J Med Chem (2007) 50 : 6485 -6492
PubMed 18052321 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 5.19 5.89

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL31634 BRIVUDINE 2.0 1 5.89
CHEMBL344738 CF1743 1 5.31
CHEMBL268634 1 4.36
CHEMBL184 ACYCLOVIR 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL31634 BRIVUDINE IC50 = 1300.0 nM 5.89
CHEMBL344738 CF1743 IC50 = 4900.0 nM 5.31
CHEMBL268634 IC50 = 44000.0 nM 4.36
CHEMBL184 ACYCLOVIR IC50 > 100000.0 nM -