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Assay Detail

CHEMBL700849

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

Functional
Cytotoxicity of compound was determined by assaying cell growth in human neoplastic cell line(KB).
5
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

KB (CHEMBL398)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis, antiproliferative, and antiviral activity of certain 4-aminopyrrolo[2,3-d]pyridazine nucleosides: an entry into a novel series of adenosine analogues.
Meade EA, Wotring LL, Drach JC, Townsend LB.
J Med Chem (1992) 35 : 526 -533
PubMed 1310744 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 5.48 6.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL267099 TUBERCIDIN 1 6.00
CHEMBL62099 1 5.52
CHEMBL611541 1 4.92
CHEMBL182 GANCICLOVIR 4.0 1 -
CHEMBL184 ACYCLOVIR 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL267099 TUBERCIDIN IC50 = 1000.0 nM 6.00
CHEMBL62099 IC50 = 3000.0 nM 5.52
CHEMBL611541 IC50 = 12000.0 nM 4.92
CHEMBL182 GANCICLOVIR IC50 > 100000.0 nM -
CHEMBL184 ACYCLOVIR IC50 > 100000.0 nM -