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Assay Detail

CHEMBL873426

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

Binding
Tested for the inhibition of HIV-2 protease
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Human immunodeficiency virus 2
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Human rhinovirus A protease (CHEMBL2857)
Type SINGLE PROTEIN
Organism Human rhinovirus sp.

Publication

Peptidomimetic inhibitors of human immunodeficiency virus protease (HIV-PR): Design, enzyme binding and selectivity, antiviral efficacy, and cell permeability properties
Sawyer T, Fisher J, Hester J, Smith C, Tomasselli A, Tarpley W, Burton P, Hui J, McQuade T, Conradi R, Bradford V, Liu L, Kinner J, Tustin J, Alexander D, Harrison A, Emmert D, Staples D, Maggiora L, Zhang Y, Poorman R, Dunna B, Rao C, Scarborough P, Lowther W, Craik C, DeCamp D, Moon J, Howe W, Heinrikson R
Bioorg Med Chem Lett (1993) 3 : 819 -824
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 1 7.52 7.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3350189 1 7.52

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3350189 Ki = 30.0 nM 7.52