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Assay Detail

CHEMBL696614

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

Functional
Concentration required to inhibit HIV-1 replication in acutely infected H9 lymphocytes by 50%
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Confidence 1 — Organism
Curated By Expert

Target

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

Publication

Anti-AIDS agents. 52. Synthesis and anti-HIV activity of hydroxymethyl (3'R,4'R)-3',4'-di-O-(S)-camphanoyl-(+)-cis-khellactone derivatives.
Xie L, Yu D, Wild C, Allaway G, Turpin J, Smith PC, Lee KH.
J Med Chem (2004) 47 : 756 -760
PubMed 14736256 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 15 7.32 9.96

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL161999 1 9.96
CHEMBL431573 1 8.82
CHEMBL423448 1 8.40
CHEMBL430615 1 7.77
CHEMBL349208 1 7.58
CHEMBL310254 1 7.54
CHEMBL269559 1 7.31
CHEMBL310494 1 7.23
CHEMBL351636 1 6.96
CHEMBL165487 1 6.83
CHEMBL350598 1 6.81
CHEMBL129 ZIDOVUDINE 4.0 1 6.73
CHEMBL350133 1 6.26
CHEMBL409338 1 6.17
CHEMBL306336 1 5.43

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL161999 EC50 = 0.11 nM 9.96
CHEMBL431573 EC50 = 1.5 nM 8.82
CHEMBL423448 EC50 = 4.0 nM 8.40
CHEMBL430615 EC50 = 17.0 nM 7.77
CHEMBL349208 EC50 = 26.0 nM 7.58
CHEMBL310254 EC50 = 29.0 nM 7.54
CHEMBL269559 EC50 = 49.0 nM 7.31
CHEMBL310494 EC50 = 59.0 nM 7.23
CHEMBL351636 EC50 = 111.0 nM 6.96
CHEMBL165487 EC50 = 148.0 nM 6.83
CHEMBL350598 EC50 = 156.0 nM 6.81
CHEMBL129 ZIDOVUDINE EC50 = 187.0 nM 6.73
CHEMBL350133 EC50 = 544.0 nM 6.26
CHEMBL409338 EC50 = 677.0 nM 6.17
CHEMBL306336 EC50 = 3670.0 nM 5.43