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

CHEMBL764539

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

Binding
Inhibition of phosphodiesterase 4
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 4 — Cell-line / Tissue
Curated By Autocuration

Target

Phosphodiesterase 4 (CHEMBL2093863)
Type PROTEIN FAMILY
Organism Homo sapiens

Publication

Synthesis and biological activities of 1-pyridylisoquinoline and 1-pyridyldihydroisoquinoline derivatives as PDE4 inhibitors.
Ukita T, Sugahara M, Terakawa Y, Kuroda T, Wada K, Nakata A, Kikkawa H, Ikezawa K, Naito K.
Bioorg Med Chem Lett (2003) 13 : 2347 -2350
PubMed 12824031 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 8.80 9.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL42126 PICLAMILAST 2.0 1 9.52
CHEMBL544766 1 9.52
CHEMBL554636 1 9.52
CHEMBL553502 1 9.40
CHEMBL542299 1 9.30
CHEMBL556179 1 9.22
CHEMBL536568 1 9.15
CHEMBL543016 1 9.15
CHEMBL539265 1 9.00
CHEMBL542650 1 8.70
CHEMBL545700 1 8.52
CHEMBL553278 1 7.16
CHEMBL63 ROLIPRAM 2.0 1 6.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL42126 PICLAMILAST IC50 = 0.3 nM 9.52
CHEMBL544766 IC50 = 0.3 nM 9.52
CHEMBL554636 IC50 = 0.3 nM 9.52
CHEMBL553502 IC50 = 0.4 nM 9.40
CHEMBL542299 IC50 = 0.5 nM 9.30
CHEMBL556179 IC50 = 0.6 nM 9.22
CHEMBL536568 IC50 = 0.7 nM 9.15
CHEMBL543016 IC50 = 0.7 nM 9.15
CHEMBL539265 IC50 = 1.0 nM 9.00
CHEMBL542650 IC50 = 2.0 nM 8.70
CHEMBL545700 IC50 = 3.0 nM 8.52
CHEMBL553278 IC50 = 70.0 nM 7.16
CHEMBL63 ROLIPRAM IC50 = 500.0 nM 6.30