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Assay Detail

CHEMBL5252950

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Binding
Binding affinity to HIV1 protease assessed as inhibition constant
20
Total Activities
20
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

Human immunodeficiency virus type 1 protease (CHEMBL243)
Type SINGLE PROTEIN
Organism Human immunodeficiency virus 1

Publication

Recent Progress in the Development of HIV-1 Protease Inhibitors for the Treatment of HIV/AIDS.
Ghosh AK, Osswald HL, Prato G.
J Med Chem (2016) 59 : 5172 -5208
PubMed 26799988 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 20 8.25 10.82

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL163 RITONAVIR 4.0 1 10.82
CHEMBL5273591 1 9.96
CHEMBL114 SAQUINAVIR 4.0 1 9.92
CHEMBL5316194 1 9.70
CHEMBL116 AMPRENAVIR 4.0 1 9.22
CHEMBL5278044 1 9.10
CHEMBL5288108 1 8.86
CHEMBL503571 1 8.77
CHEMBL584 NELFINAVIR 4.0 1 8.70
CHEMBL1230747 1 8.40
CHEMBL5287378 1 7.96
CHEMBL5286957 1 7.72
CHEMBL5285510 1 7.40
CHEMBL5274909 1 7.22
CHEMBL5281354 1 7.07
CHEMBL5271732 1 6.87
CHEMBL5287913 1 6.10
CHEMBL5274691 1 4.70
CHEMBL3577575 1 -
CHEMBL1232930 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL163 RITONAVIR Ki = 0.015 nM 10.82
CHEMBL5273591 Ki = 0.11 nM 9.96
CHEMBL114 SAQUINAVIR Ki = 0.12 nM 9.92
CHEMBL5316194 Ki = 0.2 nM 9.70
CHEMBL116 AMPRENAVIR Ki = 0.6 nM 9.22
CHEMBL5278044 Ki = 0.8 nM 9.10
CHEMBL5288108 Ki = 1.39 nM 8.86
CHEMBL503571 Ki = 1.7 nM 8.77
CHEMBL584 NELFINAVIR Ki = 2.0 nM 8.70
CHEMBL1230747 Ki = 4.0 nM 8.40
CHEMBL5287378 Ki = 11.0 nM 7.96
CHEMBL5286957 Ki = 19.0 nM 7.72
CHEMBL5285510 Ki = 40.0 nM 7.40
CHEMBL5274909 Ki = 60.0 nM 7.22
CHEMBL5281354 Ki = 85.0 nM 7.07
CHEMBL5271732 Ki = 135.0 nM 6.87
CHEMBL5287913 Ki = 801.0 nM 6.10
CHEMBL5274691 Ki = 20000.0 nM 4.70
CHEMBL3577575 Ki = 0.0058 nM -
CHEMBL1232930 Ki = 0.0059 nM -