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Assay Detail

CHEMBL689146

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

Functional
Effective concentration (anti-HIV activity) required to reduce HIV-1 induced cytopathic effect by 50%in CEM cells
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type CCRF-CEM
Confidence 1 — Organism
Curated By Intermediate

Target

Human immunodeficiency virus 1 (CHEMBL378)
Type ORGANISM
Organism Human immunodeficiency virus 1

Publication

Design, synthesis, structure-activity relationships, and molecular modeling studies of 2,3-diaryl-1,3-thiazolidin-4-ones as potent anti-HIV agents.
Barreca ML, Balzarini J, Chimirri A, De Clercq E, De Luca L, Höltje HD, Höltje M, Monforte AM, Monforte P, Pannecouque C, Rao A, Zappalà M.
J Med Chem (2002) 45 : 5410 -5413
PubMed 12431069 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 13 6.44 7.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL356190 1 7.52
CHEMBL359315 1 7.40
CHEMBL150025 1 7.11
CHEMBL151152 1 6.97
CHEMBL358883 1 6.89
CHEMBL150255 1 6.76
CHEMBL434851 1 6.62
CHEMBL625 THIABENDAZOLE 4.0 1 5.96
CHEMBL357261 1 5.88
CHEMBL346225 1 5.88
CHEMBL422322 1 5.73
CHEMBL357713 1 5.60
CHEMBL150149 1 5.38

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL356190 EC50 = 30.0 nM 7.52
CHEMBL359315 EC50 = 40.0 nM 7.40
CHEMBL150025 EC50 = 78.0 nM 7.11
CHEMBL151152 EC50 = 108.0 nM 6.97
CHEMBL358883 EC50 = 130.0 nM 6.89
CHEMBL150255 EC50 = 173.0 nM 6.76
CHEMBL434851 EC50 = 242.0 nM 6.62
CHEMBL625 THIABENDAZOLE EC50 = 1100.0 nM 5.96
CHEMBL357261 EC50 = 1310.0 nM 5.88
CHEMBL346225 EC50 = 1320.0 nM 5.88
CHEMBL422322 EC50 = 1860.0 nM 5.73
CHEMBL357713 EC50 = 2500.0 nM 5.60
CHEMBL150149 EC50 = 4130.0 nM 5.38