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Assay Detail

CHEMBL921483

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Binding
Inhibition of HIV1 integrase
13
Total Activities
13
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 Autocuration

Target

Human immunodeficiency virus type 1 integrase (CHEMBL3471)
Type SINGLE PROTEIN
Organism Human immunodeficiency virus 1

Publication

A refined pharmacophore model for HIV-1 integrase inhibitors: Optimization of potency in the 1H-benzylindole series.
De Luca L, Barreca ML, Ferro S, Iraci N, Michiels M, Christ F, Debyser Z, Witvrouw M, Chimirri A.
Bioorg Med Chem Lett (2008) 18 : 2891 -2895
PubMed 18417342 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 6.38 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL204656 ELVITEGRAVIR 4.0 1 8.40
CHEMBL254316 RALTEGRAVIR 4.0 1 8.05
CHEMBL260185 1 7.22
CHEMBL259011 1 7.10
CHEMBL261541 1 6.72
CHEMBL261714 1 6.57
CHEMBL409643 1 6.52
CHEMBL259012 1 6.07
CHEMBL260398 1 5.91
CHEMBL260619 1 5.71
CHEMBL406929 1 5.34
CHEMBL405652 1 5.32
CHEMBL263887 1 4.07

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL204656 ELVITEGRAVIR IC50 = 4.0 nM 8.40
CHEMBL254316 RALTEGRAVIR IC50 = 9.0 nM 8.05
CHEMBL260185 IC50 = 60.0 nM 7.22
CHEMBL259011 IC50 = 80.0 nM 7.10
CHEMBL261541 IC50 = 190.0 nM 6.72
CHEMBL261714 IC50 = 270.0 nM 6.57
CHEMBL409643 IC50 = 300.0 nM 6.52
CHEMBL259012 IC50 = 860.0 nM 6.07
CHEMBL260398 IC50 = 1240.0 nM 5.91
CHEMBL260619 IC50 = 1960.0 nM 5.71
CHEMBL406929 IC50 = 4600.0 nM 5.34
CHEMBL405652 IC50 = 4760.0 nM 5.32
CHEMBL263887 IC50 = 86080.0 nM 4.07