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Assay Detail

CHEMBL876992

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

Binding
Inhibition of Phosphodiesterase 3
5
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Phosphodiesterase 3 (CHEMBL2094125)
Type PROTEIN FAMILY
Organism Homo sapiens

Publication

Fused pyrimidine based inhibitors of phosphodiesterase 7 (PDE7): synthesis and initial structure-activity relationships.
Kempson J, Pitts WJ, Barbosa J, Guo J, Omotoso O, Watson A, Stebbins K, Starling GC, Dodd JH, Barrish JC, Felix R, Fischer K.
Bioorg Med Chem Lett (2005) 15 : 1829 -1833
PubMed 15780616 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 5.39 6.24

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL362451 1 6.24
CHEMBL100503 1 5.53
CHEMBL192 SILDENAFIL 4.0 1 5.16
CHEMBL183726 1 4.63
CHEMBL63 ROLIPRAM 2.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL362451 IC50 = 580.0 nM 6.24
CHEMBL100503 IC50 = 2970.0 nM 5.53
CHEMBL192 SILDENAFIL IC50 = 7000.0 nM 5.16
CHEMBL183726 IC50 = 23300.0 nM 4.63
CHEMBL63 ROLIPRAM IC50 > 10000.0 nM -