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Assay Detail

CHEMBL701804

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

Binding
Potency of compound was tested against HIV-1- containing integrase mutations (NL4-3)
1
Total Activities
1
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

Design and synthesis of 8-hydroxy-[1,6]naphthyridines as novel inhibitors of HIV-1 integrase in vitro and in infected cells.
Zhuang L, Wai JS, Embrey MW, Fisher TE, Egbertson MS, Payne LS, Guare JP, Vacca JP, Hazuda DJ, Felock PJ, Wolfe AL, Stillmock KA, Witmer MV, Moyer G, Schleif WA, Gabryelski LJ, Leonard YM, Lynch JJ, Michelson SR, Young SD.
J Med Chem (2003) 46 : 453 -456
PubMed 12570367 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 1 6.85 6.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL32865 1 6.85

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL32865 EC50 = 140.0 nM 6.85