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Assay Detail

CHEMBL4397275

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

Binding
Inhibition of humanized C57bl/6 mouse PDE4D7 UCR1 S129D mutant using cAMP as substrate by yeast myokinase/pyruvate kinase/lactate dehydrogenase-coupled fluorescence assay
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Design and Synthesis of Selective Phosphodiesterase 4D (PDE4D) Allosteric Inhibitors for the Treatment of Fragile X Syndrome and Other Brain Disorders.
Gurney ME, Nugent RA, Mo X, Sindac JA, Hagen TJ, Fox D, O'Donnell JM, Zhang C, Xu Y, Zhang HT, Groppi VE, Bailie M, White RE, Romero DL, Vellekoop AS, Walker JR, Surman MD, Zhu L, Campbell RF.
J Med Chem (2019) 62 : 4884 -4901
PubMed 31013090 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 6.88 6.88

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4541964 ZATOLMILAST 3.0 1 6.88

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4541964 ZATOLMILAST IC50 = 133.0 nM 6.88