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Assay Detail

CHEMBL4768829

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

Binding
Inhibition of FLT3 expressed in human SEMK2 cells assessed as reduction in FLT3 phosphorylation incubated for 1 hr by immunoblotting analysis
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type SEMK2
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Receptor-type tyrosine-protein kinase FLT3 (CHEMBL1974)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of orally active indirubin-3'-oxime derivatives as potent type 1 FLT3 inhibitors for acute myeloid leukemia.
Jeong P,Moon Y,Lee JH,Lee SD,Park J,Lee J,Kim J,Lee HJ,Kim NY,Choi J,Heo JD,Shin JE,Park HW,Kim YG,Han SY,Kim YC
Eur J Med Chem (2020) 195 : 112205 -112205
PubMed 32272419 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 9.54 9.54

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3301622 GILTERITINIB 4.0 1 9.54

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3301622 GILTERITINIB IC50 = 0.29 nM 9.54