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Assay Detail

CHEMBL692773

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

Functional
Effective concentration required to inhibit Tyrosine kinase deficient (TK-) Varicella-Zoster virus-induced cytopathicity by 50% in 07/01 strain HEL cell lines
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type HEL
Confidence 1 — Organism
Curated By Intermediate

Target

HEL (CHEMBL613888)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis, mechanism of action, and antiviral activity of a new series of covalent mechanism-based inhibitors of S-adenosyl-L-homocysteine hydrolase.
Guillerm G, Guillerm D, Vandenplas-Witkowki C, Rogniaux H, Carte N, Leize E, Van Dorsselaer A, De Clercq E, Lambert C.
J Med Chem (2001) 44 : 2743 -2752
PubMed 11495586 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 4 4.23 4.39

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL184 ACYCLOVIR 4.0 1 4.39
CHEMBL606446 1 4.06
CHEMBL140440 1 -
CHEMBL607985 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL184 ACYCLOVIR EC50 = 41000.0 nM 4.39
CHEMBL606446 EC50 = 87000.0 nM 4.06
CHEMBL140440 EC50 = 154000.0 nM -
CHEMBL607985 EC50 = 200000.0 nM -