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Assay Detail

CHEMBL996239

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

Functional
Antiviral activity against wild type HIV1 NL4-3 infected in MT4 cells after 6 days by MTT assay
8
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type MT4
Confidence 1 — Organism
Curated By Autocuration

Target

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

Publication

In vitro antiviral activity and cross-resistance profile of PL-100, a novel protease inhibitor of human immunodeficiency virus type 1.
Dandache S, Sévigny G, Yelle J, Stranix BR, Parkin N, Schapiro JM, Wainberg MA, Wu JJ.
Antimicrob Agents Chemother (2007) 51 : 4036 -4043
PubMed 17638694 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 8 7.63 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1163 ATAZANAVIR 4.0 1 8.40
CHEMBL114 SAQUINAVIR 4.0 1 7.92
CHEMBL168640 PPL-100 1.0 1 7.80
CHEMBL729 LOPINAVIR 4.0 1 7.72
CHEMBL584 NELFINAVIR 4.0 1 7.54
CHEMBL116 AMPRENAVIR 4.0 1 7.29
CHEMBL163 RITONAVIR 4.0 1 7.21
CHEMBL5483011 INDINAVIR 3.0 1 7.17

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1163 ATAZANAVIR EC50 = 4.0 nM 8.40
CHEMBL114 SAQUINAVIR EC50 = 12.0 nM 7.92
CHEMBL168640 PPL-100 EC50 = 16.0 nM 7.80
CHEMBL729 LOPINAVIR EC50 = 19.0 nM 7.72
CHEMBL584 NELFINAVIR EC50 = 29.0 nM 7.54
CHEMBL116 AMPRENAVIR EC50 = 51.0 nM 7.29
CHEMBL163 RITONAVIR EC50 = 61.0 nM 7.21
CHEMBL5483011 INDINAVIR EC50 = 67.0 nM 7.17