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Assay Detail

CHEMBL3870402

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

Binding
Inhibition of protease domain lacking Hepatitis C virus genotype 1b (con1) C-terminal His-tagged NS3 helicase ATP hydrolysis activity using ATP as substrate preincubated followed by substrate addition measured after 15 mins in presence of poly U RNA by malachite green-based assay
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Hepatitis C virus (isolate Con1)
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Computer-aided identification, synthesis and evaluation of substituted thienopyrimidines as novel inhibitors of HCV replication.
Bassetto M, Leyssen P, Neyts J, Yerukhimovich MM, Frick DN, Brancale A.
Eur J Med Chem (2016) 123 : 31 -47
PubMed 27474921 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 4.85 5.29

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL275938 AURINTRICARBOXYLIC ACID 1 5.29
CHEMBL3974381 1 4.40
CHEMBL3923582 1 -
CHEMBL3905109 1 -
CHEMBL3924826 1 -
CHEMBL3965951 1 -
CHEMBL3910781 1 -
CHEMBL3986658 1 -
CHEMBL3938439 1 -
CHEMBL3962118 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL275938 AURINTRICARBOXYLIC ACID IC50 = 5100.0 nM 5.29
CHEMBL3974381 IC50 = 40000.0 nM 4.40
CHEMBL3923582 IC50 > 1000000.0 nM -
CHEMBL3905109 IC50 > 1000000.0 nM -
CHEMBL3924826 IC50 - -
CHEMBL3965951 IC50 - -
CHEMBL3910781 IC50 = 780000.0 nM -
CHEMBL3986658 IC50 > 1000000.0 nM -
CHEMBL3938439 IC50 = 333000.0 nM -
CHEMBL3962118 IC50 - -