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Assay Detail

CHEMBL3789428

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

Binding
Inhibition of GST-tagged recombinant human full length PI4K3beta expressed in insect cells preincubated for 15 mins followed by addition of cold ATP/gamma32P-ATP measured after 30 mins in presence of MgCl2
10
Total Activities
10
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 Structural Characterization of Potent and Selective Inhibitors of Phosphatidylinositol 4 Kinase IIIβ.
Rutaganira FU, Fowler ML, McPhail JA, Gelman MA, Nguyen K, Xiong A, Dornan GL, Tavshanjian B, Glenn JS, Shokat KM, Burke JE.
J Med Chem (2016) 59 : 1830 -1839
PubMed 26885694 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 8.05 8.44

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3786230 1 8.44
CHEMBL3787013 1 8.38
CHEMBL3786633 1 8.36
CHEMBL3787634 1 8.28
CHEMBL3785630 1 8.26
CHEMBL3785311 1 8.15
CHEMBL3786159 1 7.80
CHEMBL1229535 1 7.77
CHEMBL3787054 1 7.64
CHEMBL3785694 1 7.44

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3786230 IC50 = 3.6 nM 8.44
CHEMBL3787013 IC50 = 4.2 nM 8.38
CHEMBL3786633 IC50 = 4.4 nM 8.36
CHEMBL3787634 IC50 = 5.3 nM 8.28
CHEMBL3785630 IC50 = 5.5 nM 8.26
CHEMBL3785311 IC50 = 7.0 nM 8.15
CHEMBL3786159 IC50 = 16.0 nM 7.80
CHEMBL1229535 IC50 = 17.0 nM 7.77
CHEMBL3787054 IC50 = 23.0 nM 7.64
CHEMBL3785694 IC50 = 36.0 nM 7.44