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Assay Detail

CHEMBL968900

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

Functional
Antiviral activity against HIV1 NL4-3 in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity by MTT assay
58
Total Activities
58
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 Autocuration

Target

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

Publication

5-Alkyl-6-benzyl-2-(2-oxo-2-phenylethylsulfanyl)pyrimidin-4(3H)-ones, a series of anti-HIV-1 agents of the dihydro-alkoxy-benzyl-oxopyrimidine family with peculiar structure-activity relationship profile.
Nawrozkij MB, Rotili D, Tarantino D, Botta G, Eremiychuk AS, Musmuca I, Ragno R, Samuele A, Zanoli S, Armand-Ugón M, Clotet-Codina I, Novakov IA, Orlinson BS, Maga G, Esté JA, Artico M, Mai A.
J Med Chem (2008) 51 : 4641 -4652
PubMed 18630898 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 58 7.14 9.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL512432 1 9.40
CHEMBL469017 1 9.00
CHEMBL511250 1 8.70
CHEMBL468352 1 8.70
CHEMBL469031 1 8.70
CHEMBL469247 1 8.40
CHEMBL469016 1 8.40
CHEMBL511424 1 8.30
CHEMBL506622 1 8.30
CHEMBL469015 1 8.30
CHEMBL512279 1 8.22
CHEMBL83140 1 8.22
CHEMBL223228 EFAVIRENZ 4.0 1 8.15
CHEMBL199234 1 8.15
CHEMBL469239 1 8.15
CHEMBL467344 1 8.15
CHEMBL469030 1 8.05
CHEMBL466949 1 7.92
CHEMBL468600 1 7.92
CHEMBL512098 1 7.82
CHEMBL468360 1 7.77
CHEMBL87451 1 7.77
CHEMBL512788 1 7.72
CHEMBL468601 1 7.70
CHEMBL467810 1 7.60
CHEMBL108396 1 7.52
CHEMBL511415 1 7.42
CHEMBL512817 1 7.35
CHEMBL468187 1 7.34
CHEMBL466948 1 7.32

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL512432 EC50 = 0.4 nM 9.40
CHEMBL469017 EC50 = 1.0 nM 9.00
CHEMBL468352 EC50 = 2.0 nM 8.70
CHEMBL469031 EC50 = 2.0 nM 8.70
CHEMBL511250 EC50 = 2.0 nM 8.70
CHEMBL469247 EC50 = 4.0 nM 8.40
CHEMBL469016 EC50 = 4.0 nM 8.40
CHEMBL511424 EC50 = 5.0 nM 8.30
CHEMBL506622 EC50 = 5.0 nM 8.30
CHEMBL469015 EC50 = 5.0 nM 8.30
CHEMBL512279 EC50 = 6.0 nM 8.22
CHEMBL83140 EC50 = 6.0 nM 8.22
CHEMBL199234 EC50 = 7.0 nM 8.15
CHEMBL223228 EFAVIRENZ EC50 = 7.0 nM 8.15
CHEMBL469239 EC50 = 7.0 nM 8.15
CHEMBL467344 EC50 = 7.0 nM 8.15
CHEMBL469030 EC50 = 9.0 nM 8.05
CHEMBL466949 EC50 = 12.0 nM 7.92
CHEMBL468600 EC50 = 12.0 nM 7.92
CHEMBL512098 EC50 = 15.0 nM 7.82
CHEMBL468360 EC50 = 17.0 nM 7.77
CHEMBL87451 EC50 = 17.0 nM 7.77
CHEMBL512788 EC50 = 19.0 nM 7.72
CHEMBL468601 EC50 = 20.0 nM 7.70
CHEMBL467810 EC50 = 25.0 nM 7.60
CHEMBL108396 EC50 = 30.0 nM 7.52
CHEMBL511415 EC50 = 38.0 nM 7.42
CHEMBL512817 EC50 = 45.0 nM 7.35
CHEMBL468187 EC50 = 46.0 nM 7.34
CHEMBL466948 EC50 = 48.0 nM 7.32
CHEMBL513342 EC50 = 60.0 nM 7.22
CHEMBL512256 EC50 = 64.0 nM 7.19
CHEMBL259493 EC50 = 67.0 nM 7.17
CHEMBL477985 EC50 = 100.0 nM 7.00
CHEMBL57 NEVIRAPINE EC50 = 130.0 nM 6.89
CHEMBL476729 EC50 = 130.0 nM 6.89
CHEMBL468599 EC50 = 200.0 nM 6.70
CHEMBL477143 EC50 = 200.0 nM 6.70
CHEMBL467363 EC50 = 290.0 nM 6.54
CHEMBL477986 EC50 = 300.0 nM 6.52
CHEMBL516745 EC50 = 400.0 nM 6.40
CHEMBL467152 EC50 = 780.0 nM 6.11
CHEMBL476524 EC50 = 1000.0 nM 6.00
CHEMBL517665 EC50 = 1000.0 nM 6.00
CHEMBL410272 EC50 = 1200.0 nM 5.92
CHEMBL468186 EC50 = 1220.0 nM 5.91
CHEMBL467362 EC50 = 1260.0 nM 5.90
CHEMBL476300 EC50 = 1400.0 nM 5.85
CHEMBL468406 EC50 = 1550.0 nM 5.81
CHEMBL468848 EC50 = 1780.0 nM 5.75