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Assay Detail

CHEMBL699509

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

Binding
Inhibitory concentration of compound against strand transfer of HIV-1 integrase in experiment 1&2
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

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

Publication

Depsides and depsidones as inhibitors of HIV-1 integrase: discovery of novel inhibitors through 3D database searching.
Neamati N, Hong H, Mazumder A, Wang S, Sunder S, Nicklaus MC, Milne GW, Proksa B, Pommier Y.
J Med Chem (1997) 40 : 942 -951
PubMed 9083483 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 4.91 5.36

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL177021 1 5.36
CHEMBL366861 FUMARPROTOCETRARIC ACID 1 5.34
CHEMBL366410 1 5.19
CHEMBL171637 PHYSODIC ACID 1 4.51
CHEMBL113835 1 4.16
CHEMBL367881 (+)-USNIC ACID 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL177021 IC50 = 4400.0 nM 5.36
CHEMBL366861 FUMARPROTOCETRARIC ACID IC50 = 4600.0 nM 5.34
CHEMBL366410 IC50 = 6500.0 nM 5.19
CHEMBL171637 PHYSODIC ACID IC50 = 30900.0 nM 4.51
CHEMBL113835 IC50 = 68500.0 nM 4.16
CHEMBL367881 (+)-USNIC ACID IC50 = 123700.0 nM -