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Assay Detail

CHEMBL1226044

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

Binding
Inhibition of human PDE4B
17
Total Activities
17
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

3',5'-cyclic-AMP phosphodiesterase 4B (CHEMBL275)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

The discovery and synthesis of highly potent subtype selective phosphodiesterase 4D inhibitors.
Aspiotis R, Deschênes D, Dubé D, Girard Y, Huang Z, Laliberté F, Liu S, Papp R, Nicholson DW, Young RN.
Bioorg Med Chem Lett (2010) 20 : 5502 -5505
PubMed 20709547 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 7.42 9.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL372575 1 9.30
CHEMBL198432 1 8.64
CHEMBL1224717 1 8.13
CHEMBL1223687 1 8.06
CHEMBL1224653 1 7.97
CHEMBL1223686 1 7.82
CHEMBL1223621 1 7.36
CHEMBL1221434 1 7.35
CHEMBL1223685 1 7.24
CHEMBL1224721 1 7.06
CHEMBL1224718 1 7.06
CHEMBL1223620 1 7.03
CHEMBL1223619 1 7.02
CHEMBL1223618 1 6.92
CHEMBL1223684 1 6.43
CHEMBL1224719 1 6.41
CHEMBL1224720 1 6.38

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL372575 IC50 = 0.5 nM 9.30
CHEMBL198432 IC50 = 2.3 nM 8.64
CHEMBL1224717 IC50 = 7.4 nM 8.13
CHEMBL1223687 IC50 = 8.7 nM 8.06
CHEMBL1224653 IC50 = 10.7 nM 7.97
CHEMBL1223686 IC50 = 15.3 nM 7.82
CHEMBL1223621 IC50 = 43.3 nM 7.36
CHEMBL1221434 IC50 = 45.0 nM 7.35
CHEMBL1223685 IC50 = 57.6 nM 7.24
CHEMBL1224721 IC50 = 86.5 nM 7.06
CHEMBL1224718 IC50 = 87.0 nM 7.06
CHEMBL1223620 IC50 = 92.7 nM 7.03
CHEMBL1223619 IC50 = 96.3 nM 7.02
CHEMBL1223618 IC50 = 120.0 nM 6.92
CHEMBL1223684 IC50 = 369.0 nM 6.43
CHEMBL1224719 IC50 = 389.0 nM 6.41
CHEMBL1224720 IC50 = 418.0 nM 6.38