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Assay Detail

CHEMBL772940

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

Binding
Inhibition of HIV-1 Protease activity
13
Total Activities
13
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 Expert

Target

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

Publication

Novel arylsulfonamides possessing sub-picomolar HIV protease activities and potent anti-HIV activity against wild-type and drug-resistant viral strains.
Miller JF, Furfine ES, Hanlon MH, Hazen RJ, Ray JA, Robinson L, Samano V, Spaltenstein A.
Bioorg Med Chem Lett (2004) 14 : 959 -963
PubMed 15013001 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 13 10.05 10.24

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL116 AMPRENAVIR 4.0 1 10.24
CHEMBL5483011 INDINAVIR 3.0 1 10.15
CHEMBL584 NELFINAVIR 4.0 1 9.77
CHEMBL435733 1 -
CHEMBL174779 1 -
CHEMBL171947 1 -
CHEMBL177470 1 -
CHEMBL433973 1 -
CHEMBL367454 1 -
CHEMBL355306 1 -
CHEMBL368496 1 -
CHEMBL353288 1 -
CHEMBL173569 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL116 AMPRENAVIR Ki = 0.057 nM 10.24
CHEMBL5483011 INDINAVIR Ki = 0.07 nM 10.15
CHEMBL584 NELFINAVIR Ki = 0.17 nM 9.77
CHEMBL435733 Ki = 0.00026 nM -
CHEMBL174779 Ki = 0.00052 nM -
CHEMBL171947 Ki = 0.00012 nM -
CHEMBL177470 Ki = 6.1e-05 nM -
CHEMBL433973 Ki = 1.4e-05 nM -
CHEMBL367454 Ki = 5.8e-05 nM -
CHEMBL355306 Ki = 4.8e-05 nM -
CHEMBL368496 Ki = 0.00016 nM -
CHEMBL353288 Ki = 5.4e-05 nM -
CHEMBL173569 Ki = 0.00021 nM -