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Assay Detail

CHEMBL905325

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

Functional
Antiviral activity against HIV1 3B-induced cytopathic effect in CEM cells assessed as inhibition of virus-induced syncytium formation
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

Synthesis and evaluation of 2-(2,6-dihalophenyl)-3-pyrimidinyl-1,3-thiazolidin-4-one analogues as anti-HIV-1 agents.
Rawal RK, Tripathi R, Katti SB, Pannecouque C, De Clercq E.
Bioorg Med Chem (2007) 15 : 3134 -3142
PubMed 17349793 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 13 5.90 7.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL390110 1 7.70
CHEMBL390956 1 7.70
CHEMBL224865 1 6.52
CHEMBL376552 1 6.10
CHEMBL53554 THIAZOLOBENZIMIDAZOLE 1 5.96
CHEMBL226271 1 5.96
CHEMBL225798 1 5.42
CHEMBL389909 1 5.41
CHEMBL225969 1 5.39
CHEMBL376385 1 5.36
CHEMBL226116 1 5.25
CHEMBL226272 1 5.24
CHEMBL225970 1 4.69

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL390110 EC50 = 20.0 nM 7.70
CHEMBL390956 EC50 = 20.0 nM 7.70
CHEMBL224865 EC50 = 300.0 nM 6.52
CHEMBL376552 EC50 = 800.0 nM 6.10
CHEMBL53554 THIAZOLOBENZIMIDAZOLE EC50 = 1100.0 nM 5.96
CHEMBL226271 EC50 = 1100.0 nM 5.96
CHEMBL225798 EC50 = 3800.0 nM 5.42
CHEMBL389909 EC50 = 3900.0 nM 5.41
CHEMBL225969 EC50 = 4100.0 nM 5.39
CHEMBL376385 EC50 = 4400.0 nM 5.36
CHEMBL226116 EC50 = 5600.0 nM 5.25
CHEMBL226272 EC50 = 5800.0 nM 5.24
CHEMBL225970 EC50 = 20300.0 nM 4.69