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Assay Detail

CHEMBL701163

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

Binding
Inhibition of human immunodeficiency virus-1 (HIV-1) integrase.
8
Total Activities
8
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 integrase (CHEMBL3471)
Type SINGLE PROTEIN
Organism Human immunodeficiency virus 1

Publication

Modeling of the inhibition of retroviral integrases by styrylquinoline derivatives.
Ouali M, Laboulais C, Leh H, Gill D, Desmaële D, Mekouar K, Zouhiri F, d'Angelo J, Auclair C, Mouscadet JF, Le Bret M.
J Med Chem (2000) 43 : 1949 -1957
PubMed 10821707 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 8 5.91 6.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL37869 1 6.52
CHEMBL39092 1 5.62
CHEMBL36586 1 5.60
CHEMBL293788 1 -
CHEMBL418303 1 -
CHEMBL58191 1 -
CHEMBL61800 1 -
CHEMBL58923 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL37869 IC50 = 300.0 nM 6.52
CHEMBL39092 IC50 = 2400.0 nM 5.62
CHEMBL36586 IC50 = 2500.0 nM 5.60
CHEMBL293788 IC50 > 100000.0 nM -
CHEMBL418303 IC50 > 100000.0 nM -
CHEMBL58191 IC50 > 100000.0 nM -
CHEMBL61800 IC50 > 100000.0 nM -
CHEMBL58923 IC50 > 100000.0 nM -