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Assay Detail

CHEMBL1025564

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

Functional
Antiviral activity against multidrug-resistant HIV1 with protease V82A, M46I, F53L, V77I, L24I, L63P mutation in human SupT1 cells assessed as viral LTR-driven luciferase activity using TZM-bl cells
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type SUP-T1
Confidence 1 — Organism
Curated By Autocuration

Target

Human immunodeficiency virus 1 (CHEMBL378)
Type ORGANISM
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
EC50 2 6.58 6.58

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL503571 1 6.58
CHEMBL449611 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL503571 EC50 = 260.0 nM 6.58
CHEMBL449611 EC50 > 1000000.0 nM -