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Assay Detail

CHEMBL4385986

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

Binding
Binding affinity to human partial length FLT3 R834Q mutant (V592 to Y969 residues) expressed in HEK293 cells measured after 1 hr by qPCR analysis
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Identification of Pyrrolo[2,3- d]pyrimidine-Based Derivatives as Potent and Orally Effective Fms-like Tyrosine Receptor Kinase 3 (FLT3) Inhibitors for Treating Acute Myelogenous Leukemia.
Yuan X, Chen Y, Zhang W, He J, Lei L, Tang M, Liu J, Li M, Dou C, Yang T, Yang L, Yang S, Wei Y, Peng A, Niu T, Xiang M, Ye H, Chen L.
J Med Chem (2019) 62 : 4158 -4173
PubMed 30939008 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Kd 1 7.99 7.99

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4439404 1 7.99

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4439404 Kd = 10.15 nM 7.99