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Assay Detail

CHEMBL996238

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Binding
Inhibition of HIV1 protease
8
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Human immunodeficiency virus 1
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Protease (CHEMBL2366517)
Type SINGLE PROTEIN
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
Ki 8 10.05 10.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL729 LOPINAVIR 4.0 1 10.85
CHEMBL163 RITONAVIR 4.0 1 10.47
CHEMBL168640 PPL-100 1.0 1 10.44
CHEMBL1163 ATAZANAVIR 4.0 1 10.41
CHEMBL114 SAQUINAVIR 4.0 1 10.10
CHEMBL116 AMPRENAVIR 4.0 1 9.93
CHEMBL584 NELFINAVIR 4.0 1 9.51
CHEMBL5483011 INDINAVIR 3.0 1 8.71

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL729 LOPINAVIR Ki = 0.014 nM 10.85
CHEMBL163 RITONAVIR Ki = 0.034 nM 10.47
CHEMBL168640 PPL-100 Ki = 0.036 nM 10.44
CHEMBL1163 ATAZANAVIR Ki = 0.039 nM 10.41
CHEMBL114 SAQUINAVIR Ki = 0.08 nM 10.10
CHEMBL116 AMPRENAVIR Ki = 0.117 nM 9.93
CHEMBL584 NELFINAVIR Ki = 0.306 nM 9.51
CHEMBL5483011 INDINAVIR Ki = 1.945 nM 8.71