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Assay Detail

CHEMBL832835

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

Binding
Inhibition of human Phosphodiesterase 5; IC50 range 0.03-0.3 nM
1
Total Activities
1
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

New pyrazolo[1',5':1,6]pyrimido[4,5-d]pyridazin-4(3H)-ones as potent and selective PDE5 inhibitors.
Feixas J, Giovannoni MP, Vergelli C, Gavaldà A, Cesari N, Graziano A, Dal Piaz V.
Bioorg Med Chem Lett (2005) 15 : 2381 -2384
PubMed 15837329 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 9.52 9.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL139998 1 9.52

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL139998 IC50 = 0.3 nM 9.52