Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL891424

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

Functional
Antiviral activity against HIV1 RT 181C mutant assessed as inhibition of viral-induced cytopathicity in MT4 cells by MTT method
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Human immunodeficiency virus 1
Cell Type MT4
Confidence 1 — Organism
Curated By Intermediate

Target

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

Publication

Structure-activity relationship in the 3-iodo-4-phenoxypyridinone (IOPY) series: The nature of the C-3 substituent on anti-HIV activity.
Benjahad A, Oumouch S, Guillemont J, Pasquier E, Mabire D, Andries K, Nguyen CH, Grierson DS.
Bioorg Med Chem Lett (2007) 17 : 712 -716
PubMed 17157017 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 7.26 8.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL223228 EFAVIRENZ 4.0 1 8.70
CHEMBL233664 1 7.70
CHEMBL234283 1 7.70
CHEMBL233452 1 7.50
CHEMBL397934 1 7.40
CHEMBL395522 1 7.40
CHEMBL233663 1 7.30
CHEMBL234077 1 7.20
CHEMBL234282 1 7.00
CHEMBL233662 1 6.80
CHEMBL233453 1 6.80
CHEMBL234285 1 6.80
CHEMBL234284 1 6.10

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL223228 EFAVIRENZ IC50 = 1.99 nM 8.70
CHEMBL233664 IC50 = 19.9 nM 7.70
CHEMBL234283 IC50 = 19.9 nM 7.70
CHEMBL233452 IC50 = 31.6 nM 7.50
CHEMBL397934 IC50 = 39.8 nM 7.40
CHEMBL395522 IC50 = 39.8 nM 7.40
CHEMBL233663 IC50 = 50.1 nM 7.30
CHEMBL234077 IC50 = 63.1 nM 7.20
CHEMBL234282 IC50 = 100.0 nM 7.00
CHEMBL233662 IC50 = 158.0 nM 6.80
CHEMBL233453 IC50 = 158.0 nM 6.80
CHEMBL234285 IC50 = 158.0 nM 6.80
CHEMBL234284 IC50 = 794.0 nM 6.10