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Assay Detail

CHEMBL5337346

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

Binding
Inhibition of N-terminal HA-tagged recombinant wild-type human MLK3 overexpressed in HEK293A cells preincubated for 10 mins followed by [gamma-32P]ATP addition measured after 20 mins by immunoblot analysis
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HEK293-A
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Mitogen-activated protein kinase kinase kinase 11 (CHEMBL2708)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, synthesis of new 3H-imidazo[4,5-b]pyridine derivatives and evaluation of their inhibitory properties as mixed lineage kinase 3 inhibitors.
Yoon HR, Balupuri A, Lee J, Lee C, Son DH, Jeoung RG, Kim KA, Choi S, Kang NS.
Bioorg Med Chem Lett (2024) 101 : 129652 -129652
PubMed 38346577 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 8.30 8.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL281948 K-252A 1 8.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL281948 K-252A IC50 = 5.0 nM 8.30