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Assay Detail

CHEMBL656738

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

Functional
Antiviral activity evaluated as the ability to inhibit the replication of HIV-2 in human T-lymphocytic cells (CEM)
14
Total Activities
14
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

cycloSal-Pronucleotides of 2'-fluoro-ara- and 2'-fluoro-ribo-2',3'- dideoxyadenosine as a strategy to bypass a metabolic blockade.
Meier C, Knispel T, Marquez VE, Siddiqui MA, De Clercq E, Balzarini J.
J Med Chem (1999) 42 : 1615 -1624
PubMed 10229630 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 14 5.14 6.58

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL991 STAVUDINE 4.0 1 6.58
CHEMBL295071 1 5.73
CHEMBL2111583 1 5.48
CHEMBL297105 1 5.45
CHEMBL23094 1 5.34
CHEMBL44302 1 5.25
CHEMBL2112391 1 4.90
CHEMBL40874 1 4.89
CHEMBL42392 1 4.60
CHEMBL432291 1 4.52
CHEMBL42467 1 4.50
CHEMBL501916 LODENOSINE 2.0 1 4.40
CHEMBL2114462 1 -
CHEMBL42429 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL991 STAVUDINE EC50 = 260.0 nM 6.58
CHEMBL295071 EC50 = 1850.0 nM 5.73
CHEMBL2111583 EC50 = 3300.0 nM 5.48
CHEMBL297105 EC50 = 3570.0 nM 5.45
CHEMBL23094 EC50 = 4550.0 nM 5.34
CHEMBL44302 EC50 = 5670.0 nM 5.25
CHEMBL2112391 EC50 = 12500.0 nM 4.90
CHEMBL40874 EC50 = 13000.0 nM 4.89
CHEMBL42392 EC50 = 25000.0 nM 4.60
CHEMBL432291 EC50 = 30000.0 nM 4.52
CHEMBL42467 EC50 = 31700.0 nM 4.50
CHEMBL501916 LODENOSINE EC50 = 40000.0 nM 4.40
CHEMBL2114462 EC50 > 250000.0 nM -
CHEMBL42429 EC50 > 250000.0 nM -