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Assay Detail

CHEMBL5620535

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

Binding
Inhibition of recombinant PDE7A1 (130 to 482 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3) using [3H]cAMP as substrate incubated for 15 mins by liquid scintillation method
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

High affinity 3',5'-cyclic-AMP phosphodiesterase 7A (CHEMBL3012)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Advances in the development of phosphodiesterase 7 inhibitors.
Huang JX, Zhu BL, Xu JP, Zhou ZZ.
Eur J Med Chem (2023) 250 : 115194 -115194
PubMed 36796299 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 6.34 6.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5630424 1 6.85
CHEMBL484928 1 6.58
CHEMBL1911416 1 6.09
CHEMBL4756052 1 5.85

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5630424 IC50 = 142.0 nM 6.85
CHEMBL484928 IC50 = 260.0 nM 6.58
CHEMBL1911416 IC50 = 820.0 nM 6.09
CHEMBL4756052 IC50 = 1400.0 nM 5.85