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

CHEMBL827094

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

Binding
In vitro inhibition of human Phosphodiesterase 5
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Expert

Target

cGMP-specific 3',5'-cyclic phosphodiesterase (CHEMBL1827)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Spiroquinazolinones as novel, potent, and selective PDE7 inhibitors. Part 1.
Lorthiois E, Bernardelli P, Vergne F, Oliveira C, Mafroud AK, Proust E, Heuze L, Moreau F, Idrissi M, Tertre A, Bertin B, Coupe M, Wrigglesworth R, Descours A, Soulard P, Berna P.
Bioorg Med Chem Lett (2004) 14 : 4623 -4626
PubMed 15324876 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 4.69 5.07

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL185304 1 5.07
CHEMBL185208 1 5.02
CHEMBL427505 1 4.90
CHEMBL184945 1 4.71
CHEMBL185370 1 4.28
CHEMBL361469 1 4.17
CHEMBL185588 1 -
CHEMBL366149 1 -
CHEMBL363084 1 -
CHEMBL427513 1 -
CHEMBL182617 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL185304 IC50 = 8500.0 nM 5.07
CHEMBL185208 IC50 = 9470.0 nM 5.02
CHEMBL427505 IC50 = 12600.0 nM 4.90
CHEMBL184945 IC50 = 19300.0 nM 4.71
CHEMBL185370 IC50 = 52400.0 nM 4.28
CHEMBL361469 IC50 = 68400.0 nM 4.17
CHEMBL185588 IC50 > 101000.0 nM -
CHEMBL366149 IC50 > 67300.0 nM -
CHEMBL363084 IC50 > 101000.0 nM -
CHEMBL427513 IC50 > 50700.0 nM -
CHEMBL182617 IC50 > 84900.0 nM -