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Assay Detail

CHEMBL650617

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

Functional
Tested for in vitro drug concentration which produces 50% survival of HIV-1 infected CEM cells relative to uninfected untreated controls
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

CCRF-CEM (CHEMBL382)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and antiviral (HIV-1, HBV) activities of 5-halo-6-methoxy(or azido)-5,6-dihydro-3'-fluoro-3'-deoxythymidine diastereomers. Potential prodrugs to 3'-fluoro-3'-deoxythymidine.
Kumar R, Wang L, Wiebe LI, Knaus EE.
J Med Chem (1994) 37 : 3554 -3560
PubMed 7932583 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 9 7.17 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL105318 ALOVUDINE 2.0 1 9.00
CHEMBL129 ZIDOVUDINE 4.0 1 8.52
CHEMBL116767 1 8.49
CHEMBL121850 1 8.43
CHEMBL118427 1 8.28
CHEMBL116319 1 7.84
CHEMBL119051 1 5.26
CHEMBL334183 1 4.42
CHEMBL119448 1 4.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL105318 ALOVUDINE EC50 = 1.0 nM 9.00
CHEMBL129 ZIDOVUDINE EC50 = 3.0 nM 8.52
CHEMBL116767 EC50 = 3.25 nM 8.49
CHEMBL121850 EC50 = 3.75 nM 8.43
CHEMBL118427 EC50 = 5.25 nM 8.28
CHEMBL116319 EC50 = 14.5 nM 7.84
CHEMBL119051 EC50 = 5550.0 nM 5.26
CHEMBL334183 EC50 = 37900.0 nM 4.42
CHEMBL119448 EC50 = 50000.0 nM 4.30