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Assay Detail

CHEMBL972657

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

Binding
Inhibition of HCV 1b isolate BK NS5B Cdelta21 polymerase
16
Total Activities
16
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Discovery of (R)-6-cyclopentyl-6-(2-(2,6-diethylpyridin-4-yl)ethyl)-3-((5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)methyl)-4-hydroxy-5,6-dihydropyran-2-one (PF-00868554) as a potent and orally available hepatitis C virus polymerase inhibitor.
Li H, Tatlock J, Linton A, Gonzalez J, Jewell T, Patel L, Ludlum S, Drowns M, Rahavendran SV, Skor H, Hunter R, Shi ST, Herlihy KJ, Parge H, Hickey M, Yu X, Chau F, Nonomiya J, Lewis C.
J Med Chem (2009) 52 : 1255 -1258
PubMed 19209845 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 16 7.95 8.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL230743 1 8.70
CHEMBL230744 1 8.52
CHEMBL514640 1 8.52
CHEMBL509746 1 8.30
CHEMBL522658 1 8.22
CHEMBL524103 1 8.15
CHEMBL490672 FILIBUVIR 3.0 1 8.15
CHEMBL515872 1 8.10
CHEMBL489476 1 8.10
CHEMBL474322 1 8.00
CHEMBL522458 1 8.00
CHEMBL489295 1 7.92
CHEMBL490671 1 7.80
CHEMBL472914 1 7.06
CHEMBL516051 1 6.85
CHEMBL472913 1 6.75

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL230743 IC50 = 2.0 nM 8.70
CHEMBL230744 IC50 = 3.0 nM 8.52
CHEMBL514640 IC50 = 3.0 nM 8.52
CHEMBL509746 IC50 = 5.0 nM 8.30
CHEMBL522658 IC50 = 6.0 nM 8.22
CHEMBL524103 IC50 = 7.0 nM 8.15
CHEMBL490672 FILIBUVIR IC50 = 7.0 nM 8.15
CHEMBL515872 IC50 = 8.0 nM 8.10
CHEMBL489476 IC50 = 8.0 nM 8.10
CHEMBL474322 IC50 = 10.0 nM 8.00
CHEMBL522458 IC50 = 10.0 nM 8.00
CHEMBL489295 IC50 = 12.0 nM 7.92
CHEMBL490671 IC50 = 16.0 nM 7.80
CHEMBL472914 IC50 = 88.0 nM 7.06
CHEMBL516051 IC50 = 140.0 nM 6.85
CHEMBL472913 IC50 = 180.0 nM 6.75