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Assay Detail

CHEMBL689115

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

Functional
Inhibitory concentration required to inhibit uninfected H9 cell growth by 50%
8
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type H9
Confidence 1 — Organism
Curated By Intermediate

Target

H9 (CHEMBL614806)
Type CELL-LINE
Organism Homo sapiens

Publication

Anti-AIDS agents. Part 47: Synthesis and anti-HIV activity of 3-substituted 3',4'-Di-O-(S)-camphanoyl-(3'R,4'R)-(+)-cis-khellactone derivatives.
Xie L, Allaway G, Wild C, Kilgore N, Lee KH.
Bioorg Med Chem Lett (2001) 11 : 2291 -2293
PubMed 11527717 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 8 4.89 5.50

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL308801 1 5.50
CHEMBL430615 1 5.48
CHEMBL310494 1 5.47
CHEMBL409338 1 4.48
CHEMBL269559 1 4.46
CHEMBL310254 1 4.45
CHEMBL306336 1 4.37
CHEMBL129 ZIDOVUDINE 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL308801 IC50 = 3200.0 nM 5.50
CHEMBL430615 IC50 = 3340.0 nM 5.48
CHEMBL310494 IC50 = 3380.0 nM 5.47
CHEMBL409338 IC50 = 32810.0 nM 4.48
CHEMBL269559 IC50 = 35000.0 nM 4.46
CHEMBL310254 IC50 = 35350.0 nM 4.45
CHEMBL306336 IC50 = 43010.0 nM 4.37
CHEMBL129 ZIDOVUDINE IC50 = 1875000.0 nM -