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Assay Detail

CHEMBL653197

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

Functional
Concentration which produces a 50% survival of HIV-1 infected cells relative to uninfected control CEM-SS cells (in vitro anti-HIV activity)
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type CEM-SS
Confidence 1 — Organism
Curated By Intermediate

Target

CEM-SS (CHEMBL614548)
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
EC50 9 8.28 9.33

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL105916 1 9.33
CHEMBL110091 1 8.74
CHEMBL129 ZIDOVUDINE 4.0 1 8.72
CHEMBL107099 1 8.72
CHEMBL418833 1 8.54
CHEMBL107535 1 8.28
CHEMBL320557 1 7.89
CHEMBL418812 1 7.20
CHEMBL316514 1 7.07

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL105916 EC50 = 0.47 nM 9.33
CHEMBL110091 EC50 = 1.8 nM 8.74
CHEMBL129 ZIDOVUDINE EC50 = 1.9 nM 8.72
CHEMBL107099 EC50 = 1.9 nM 8.72
CHEMBL418833 EC50 = 2.9 nM 8.54
CHEMBL107535 EC50 = 5.2 nM 8.28
CHEMBL320557 EC50 = 13.0 nM 7.89
CHEMBL418812 EC50 = 63.0 nM 7.20
CHEMBL316514 EC50 = 85.0 nM 7.07