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Assay Detail

CHEMBL1831858

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

Functional
Antiviral activity against 100 TCID50 wild type HIV1 LAI infected in human PBMC assessed as reduction in viral replication measured on day 7 post infection by reverse transcriptase activity
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Acyclic nucleoside thiophosphonates as potent inhibitors of HIV and HBV replication.
Barral K, Weck C, Payrot N, Roux L, Durafour C, Zoulim F, Neyts J, Balzarini J, Canard B, Priet S, Alvarez K.
Eur J Med Chem (2011) 46 : 4281 -4288
PubMed 21803462 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 4 5.30 5.50

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL484 ADEFOVIR 3.0 1 5.50
CHEMBL483 TENOFOVIR ANHYDROUS 3.0 1 5.47
CHEMBL1830069 1 5.38
CHEMBL1830068 1 4.85

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL484 ADEFOVIR EC50 = 3200.0 nM 5.50
CHEMBL483 TENOFOVIR ANHYDROUS EC50 = 3400.0 nM 5.47
CHEMBL1830069 EC50 = 4200.0 nM 5.38
CHEMBL1830068 EC50 = 14000.0 nM 4.85