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Assay Detail

CHEMBL711604

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

Functional
Compound was tested for anti-rhinovirus type 1B activity in a plaque inhibition assay using monolayers of M-HeLa cells
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type HeLa
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Synthesis and structure-activity relationships of 2-substituted-6-(dimethylamino)-9-(4-methylbenzyl)-9H-purines with antirhinovirus activity.
Kelley JL, Linn JA, Selway JW.
J Med Chem (1989) 32 : 218 -224
PubMed 2535875 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 5.89 7.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL283830 1 7.52
CHEMBL416937 1 7.10
CHEMBL305661 1 6.47
CHEMBL306857 1 6.47
CHEMBL72589 1 6.10
CHEMBL72360 1 5.96
CHEMBL538916 1 5.64
CHEMBL431375 1 5.33
CHEMBL403464 1 5.07
CHEMBL71076 1 4.60
CHEMBL70888 1 4.51

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL283830 IC50 = 30.2 nM 7.52
CHEMBL416937 IC50 = 79.43 nM 7.10
CHEMBL305661 IC50 = 338.84 nM 6.47
CHEMBL306857 IC50 = 338.84 nM 6.47
CHEMBL72589 IC50 = 794.33 nM 6.10
CHEMBL72360 IC50 = 1096.48 nM 5.96
CHEMBL538916 IC50 = 2290.87 nM 5.64
CHEMBL431375 IC50 = 4677.35 nM 5.33
CHEMBL403464 IC50 = 8511.38 nM 5.07
CHEMBL71076 IC50 = 25118.86 nM 4.60
CHEMBL70888 IC50 = 30902.95 nM 4.51