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Assay Detail

CHEMBL704807

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

Functional
Compound was evaluated for the inhibition of KB cell growth determined in quadruplicate assay
11
Total Activities
11
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

Design, synthesis, and antiviral activity of certain 2,5,6-trihalo-1-(beta-D-ribofuranosyl)benzimidazoles.
Townsend LB, Devivar RV, Turk SR, Nassiri MR, Drach JC.
J Med Chem (1995) 38 : 4098 -4105
PubMed 7562945 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 4.51 4.72

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL134238 1 4.72
CHEMBL605800 1 4.64
CHEMBL3143098 1 4.60
CHEMBL375530 DICHLORORIBOBENZIMIDAZOLE 1 4.44
CHEMBL603513 1 4.40
CHEMBL133003 1 4.25
CHEMBL3143099 1 -
CHEMBL182 GANCICLOVIR 4.0 1 -
CHEMBL513232 1 -
CHEMBL2093921 1 -
CHEMBL71905 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL134238 IC50 = 19000.0 nM 4.72
CHEMBL605800 IC50 = 23000.0 nM 4.64
CHEMBL3143098 IC50 = 25000.0 nM 4.60
CHEMBL375530 DICHLORORIBOBENZIMIDAZOLE IC50 = 36000.0 nM 4.44
CHEMBL603513 IC50 = 40000.0 nM 4.40
CHEMBL133003 IC50 = 56000.0 nM 4.25
CHEMBL3143099 IC50 > 100000.0 nM -
CHEMBL182 GANCICLOVIR IC50 > 100000.0 nM -
CHEMBL513232 IC50 = 210000.0 nM -
CHEMBL2093921 IC50 > 100000.0 nM -
CHEMBL71905 IC50 > 100000.0 nM -