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Assay Detail

CHEMBL1025565

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Binding
Inhibition of wild type HIV1 protease
2
Total Activities
1
Compounds Tested
2
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

A copper(I)-catalyzed 1,2,3-triazole azide-alkyne click compound is a potent inhibitor of a multidrug-resistant HIV-1 protease variant.
Giffin MJ, Heaslet H, Brik A, Lin YC, Cauvi G, Wong CH, McRee DE, Elder JH, Stout CD, Torbett BE.
J Med Chem (2008) 51 : 6263 -6270
PubMed 18823110 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 8.22 8.22
Ki 1 8.57 8.57

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL503571 2 8.57

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL503571 Ki = 2.7 nM 8.57
CHEMBL503571 IC50 = 6.0 nM 8.22