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Assay Detail

CHEMBL877269

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

ADMET
Concentration which results in 50% survival of uninfected untreated control C8166 cells (cytotoxicity of the compound)
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type ADMET
Organism Homo sapiens
Cell Type C8166
Confidence 1 — Organism
Curated By Intermediate

Target

C8166 (CHEMBL614533)
Type CELL-LINE
Organism Homo sapiens

Publication

Quinoxalinylethylpyridylthioureas (QXPTs) as potent non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors. Further SAR studies and identification of a novel orally bioavailable hydrazine-based antiviral agent.
Campiani G, Aiello F, Fabbrini M, Morelli E, Ramunno A, Armaroli S, Nacci V, Garofalo A, Greco G, Novellino E, Maga G, Spadari S, Bergamini A, Ventura L, Bongiovanni B, Capozzi M, Bolacchi F, Marini S, Coletta M, Guiso G, Caccia S.
J Med Chem (2001) 44 : 305 -315
PubMed 11462972 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 4.54 4.77

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL108221 1 4.77
CHEMBL58711 TIVIRAPINE 2.0 1 4.30
CHEMBL129 ZIDOVUDINE 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL108221 IC50 = 17000.0 nM 4.77
CHEMBL58711 TIVIRAPINE IC50 = 50000.0 nM 4.30
CHEMBL129 ZIDOVUDINE IC50 > 100000.0 nM -