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Assay Detail

CHEMBL811287

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

Binding
Inhibition of HSV-2 thymidine kinase, 2 uM [3H]thymidine and ATP as phosphate donor
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Human alphaherpesvirus 2
Confidence 9 — Direct single protein target
Curated By Expert

Target

Thymidine kinase (CHEMBL3415)
Type SINGLE PROTEIN
Organism Human herpesvirus 2

Publication

Synthesis, properties, and pharmacokinetic studies of N2-phenylguanine derivatives as inhibitors of herpes simplex virus thymidine kinases.
Xu H, Maga G, Focher F, Smith ER, Spadari S, Gambino J, Wright GE.
J Med Chem (1995) 38 : 49 -57
PubMed 7837239 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 5.65 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL405761 1 7.00
CHEMBL152338 1 6.75
CHEMBL153866 1 6.33
CHEMBL152256 1 6.00
CHEMBL347128 1 5.92
CHEMBL152475 1 5.80
CHEMBL287727 1 5.80
CHEMBL3143447 1 5.70
CHEMBL406254 1 5.67
CHEMBL3143935 1 5.60
CHEMBL154209 1 5.57
CHEMBL262742 1 5.46
CHEMBL152257 1 5.41
CHEMBL152838 1 5.20
CHEMBL152575 1 5.01
CHEMBL436424 1 4.69
CHEMBL157220 1 4.16

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL405761 IC50 = 100.0 nM 7.00
CHEMBL152338 IC50 = 180.0 nM 6.75
CHEMBL153866 IC50 = 470.0 nM 6.33
CHEMBL152256 IC50 = 1000.0 nM 6.00
CHEMBL347128 IC50 = 1200.0 nM 5.92
CHEMBL152475 IC50 = 1600.0 nM 5.80
CHEMBL287727 IC50 = 1600.0 nM 5.80
CHEMBL3143447 IC50 = 2000.0 nM 5.70
CHEMBL406254 IC50 = 2150.0 nM 5.67
CHEMBL3143935 IC50 = 2500.0 nM 5.60
CHEMBL154209 IC50 = 2700.0 nM 5.57
CHEMBL262742 IC50 = 3500.0 nM 5.46
CHEMBL152257 IC50 = 3900.0 nM 5.41
CHEMBL152838 IC50 = 6300.0 nM 5.20
CHEMBL152575 IC50 = 9800.0 nM 5.01
CHEMBL436424 IC50 = 20400.0 nM 4.69
CHEMBL157220 IC50 = 70000.0 nM 4.16