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Assay Detail

CHEMBL932292

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

Binding
Inhibition of human ERG
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Publication

Design and synthesis of bicyclic pyrimidinones as potent and orally bioavailable HIV-1 integrase inhibitors.
Muraglia E, Kinzel O, Gardelli C, Crescenzi B, Donghi M, Ferrara M, Nizi E, Orvieto F, Pescatore G, Laufer R, Gonzalez-Paz O, Di Marco A, Fiore F, Monteagudo E, Fonsi M, Felock PJ, Rowley M, Summa V.
J Med Chem (2008) 51 : 861 -874
PubMed 18217703 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 4.70 4.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL408479 1 4.70
CHEMBL408962 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL408479 IC50 = 20000.0 nM 4.70
CHEMBL408962 IC50 > 10000.0 nM -