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Assay Detail

CHEMBL691400

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

Binding
Inhibition of HIV-1 Protease
14
Total Activities
14
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

Cyclic sulfone-3-carboxamides as novel P2-ligands for Ro 31-8959 based HIV-1 protease inhibitors
Ghosh AK, Thompson WJ, Munson PM, Liu W, Huff JR
Bioorg Med Chem Lett (1995) 5 : 83 -88
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 6.81 8.04

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL355316 1 8.04
CHEMBL436252 1 7.63
CHEMBL354884 1 7.26
CHEMBL273317 1 7.12
CHEMBL170195 1 7.11
CHEMBL352747 1 7.00
CHEMBL275389 1 6.85
CHEMBL354379 1 6.78
CHEMBL354805 1 6.71
CHEMBL354169 1 6.70
CHEMBL354309 1 6.47
CHEMBL355133 1 6.19
CHEMBL18086 1 5.76
CHEMBL18603 1 5.68

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL355316 IC50 = 9.2 nM 8.04
CHEMBL436252 IC50 = 23.5 nM 7.63
CHEMBL354884 IC50 = 54.7 nM 7.26
CHEMBL273317 IC50 = 76.0 nM 7.12
CHEMBL170195 IC50 = 78.4 nM 7.11
CHEMBL352747 IC50 = 98.8 nM 7.00
CHEMBL275389 IC50 = 140.0 nM 6.85
CHEMBL354379 IC50 = 167.4 nM 6.78
CHEMBL354805 IC50 = 193.0 nM 6.71
CHEMBL354169 IC50 = 200.0 nM 6.70
CHEMBL354309 IC50 = 342.0 nM 6.47
CHEMBL355133 IC50 = 650.0 nM 6.19
CHEMBL18086 IC50 = 1745.0 nM 5.76
CHEMBL18603 IC50 = 2068.0 nM 5.68