Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL3294392

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

Binding
Inhibition of FLT3 kinase (unknown origin)
12
Total Activities
12
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

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

Publication

Discovery of thienopyrimidine-based FLT3 inhibitors from the structural modification of known IKKβ inhibitors.
Park CH, Lee C, Yang JS, Joe BY, Chun K, Kim H, Kim HY, Kang JS, Lee JI, Kim MH, Han G.
Bioorg Med Chem Lett (2014) 24 : 2655 -2660
PubMed 24813730 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 6.68 7.19

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3290626 1 7.19
CHEMBL3290634 1 7.07
CHEMBL124660 TANDUTINIB 2.0 1 6.99
CHEMBL576982 QUIZARTINIB 4.0 1 6.92
CHEMBL3290631 1 6.88
CHEMBL3290625 1 6.76
CHEMBL3290633 1 6.76
CHEMBL3290628 1 6.68
CHEMBL3290629 1 6.31
CHEMBL3290632 1 6.27
CHEMBL3290627 1 6.17
CHEMBL3290630 1 6.12

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3290626 IC50 = 65.0 nM 7.19
CHEMBL3290634 IC50 = 85.0 nM 7.07
CHEMBL124660 TANDUTINIB IC50 = 102.0 nM 6.99
CHEMBL576982 QUIZARTINIB IC50 = 120.0 nM 6.92
CHEMBL3290631 IC50 = 133.0 nM 6.88
CHEMBL3290625 IC50 = 175.0 nM 6.76
CHEMBL3290633 IC50 = 175.0 nM 6.76
CHEMBL3290628 IC50 = 208.0 nM 6.68
CHEMBL3290629 IC50 = 488.0 nM 6.31
CHEMBL3290632 IC50 = 540.0 nM 6.27
CHEMBL3290627 IC50 = 673.0 nM 6.17
CHEMBL3290630 IC50 = 750.0 nM 6.12