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Assay Detail

CHEMBL2388598

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

Functional
Antiviral activity against wild type HIV-1 3B infected in human CEM cells assessed as inhibition of syncytia formation after 4 days by microscopic analysis
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type CCRF-CEM
Confidence 1 — Organism
Curated By Autocuration

Target

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

Publication

Ester prodrugs of acyclic nucleoside thiophosphonates compared to phosphonates: synthesis, antiviral activity and decomposition study.
Roux L, Priet S, Payrot N, Weck C, Fournier M, Zoulim F, Balzarini J, Canard B, Alvarez K.
Eur J Med Chem (2013) 63 : 869 -881
PubMed 23603046 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 4 7.40 7.80

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1538 TENOFOVIR DISOPROXIL 4.0 1 7.80
CHEMBL922 ADEFOVIR DIPIVOXIL 4.0 1 7.35
CHEMBL2386206 1 7.04
CHEMBL2386205 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1538 TENOFOVIR DISOPROXIL EC50 = 16.0 nM 7.80
CHEMBL922 ADEFOVIR DIPIVOXIL EC50 = 45.0 nM 7.35
CHEMBL2386206 EC50 = 92.0 nM 7.04
CHEMBL2386205 EC50 >= 200.0 nM -