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Assay Detail

CHEMBL897354

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

Functional
Antiviral activity against HIV1 with reverse transcriptase L100I mutation in CEM cells assessed as inhibition of virus-induced giant cell formation
5
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type CCRF-CEM
Confidence 1 — Organism
Curated By Intermediate

Target

Human immunodeficiency virus 1 (CHEMBL378)
Type ORGANISM
Organism Human immunodeficiency virus 1

Publication

Discovery of novel benzimidazolones as potent non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strains.
Barreca ML, Rao A, De Luca L, Iraci N, Monforte AM, Maga G, De Clercq E, Pannecouque C, Balzarini J, Chimirri A.
Bioorg Med Chem Lett (2007) 17 : 1956 -1960
PubMed 17276064 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 5 7.00 8.22

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL234401 1 8.22
CHEMBL234400 1 7.31
CHEMBL223228 EFAVIRENZ 4.0 1 7.24
CHEMBL57 NEVIRAPINE 4.0 1 6.70
CHEMBL393003 1 5.51

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL234401 EC50 = 6.0 nM 8.22
CHEMBL234400 EC50 = 49.0 nM 7.31
CHEMBL223228 EFAVIRENZ EC50 = 57.3 nM 7.24
CHEMBL57 NEVIRAPINE EC50 = 199.0 nM 6.70
CHEMBL393003 EC50 = 3100.0 nM 5.51