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Assay Detail

CHEMBL891625

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

Functional
Antiviral activity against HIV1 3B in MT4 cells assessed as inhibition of virus-induced syncytium formation after 5 days
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type MT4
Confidence 1 — Organism
Curated By Intermediate

Target

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

Publication

Design, synthesis, and evaluation of 2-aryl-3-heteroaryl-1,3-thiazolidin-4-ones as anti-HIV agents.
Rawal RK, Tripathi R, Katti SB, Pannecouque C, De Clercq E.
Bioorg Med Chem (2007) 15 : 1725 -1731
PubMed 17178227 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 17 6.01 7.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL243902 1 7.52
CHEMBL242378 1 6.58
CHEMBL53554 THIAZOLOBENZIMIDAZOLE 1 6.46
CHEMBL395532 1 6.34
CHEMBL243004 1 6.12
CHEMBL395294 1 5.95
CHEMBL395056 1 5.87
CHEMBL243218 1 5.82
CHEMBL396992 1 5.82
CHEMBL395531 1 5.57
CHEMBL395295 1 5.50
CHEMBL244283 1 4.59
CHEMBL397017 1 -
CHEMBL244282 1 -
CHEMBL395768 1 -
CHEMBL244281 1 -
CHEMBL242168 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL243902 EC50 = 30.0 nM 7.52
CHEMBL242378 EC50 = 260.0 nM 6.58
CHEMBL53554 THIAZOLOBENZIMIDAZOLE EC50 = 350.0 nM 6.46
CHEMBL395532 EC50 = 460.0 nM 6.34
CHEMBL243004 EC50 = 760.0 nM 6.12
CHEMBL395294 EC50 = 1120.0 nM 5.95
CHEMBL395056 EC50 = 1340.0 nM 5.87
CHEMBL243218 EC50 = 1510.0 nM 5.82
CHEMBL396992 EC50 = 1510.0 nM 5.82
CHEMBL395531 EC50 = 2670.0 nM 5.57
CHEMBL395295 EC50 = 3200.0 nM 5.50
CHEMBL244283 EC50 = 25730.0 nM 4.59
CHEMBL397017 EC50 > 327830.0 nM -
CHEMBL244282 EC50 > 51010.0 nM -
CHEMBL395768 EC50 > 18880.0 nM -
CHEMBL244281 EC50 > 53570.0 nM -
CHEMBL242168 EC50 > 125200.0 nM -