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Assay Detail

CHEMBL4839014

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

Binding
Inhibition of FYK Y379 mutant phosphorylation in human MDA-MB-231 cells by in-cell western blot assay
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HCT-116
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Identification of Thieno[3,2-<i>d</i>]pyrimidine Derivatives as Dual Inhibitors of Focal Adhesion Kinase and FMS-like Tyrosine Kinase 3.
Cho H, Shin I, Yoon H, Jeon E, Lee J, Kim Y, Ryu S, Song C, Kwon NH, Moon Y, Kim S, Kim ND, Choi HG, Sim T.
J Med Chem (2021) 64 : 11934 -11957
PubMed 34324343 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 6.58 6.58

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4851157 1 6.58
CHEMBL4873104 1 6.58
CHEMBL4846921 1 6.58

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4851157 IC50 = 260.0 nM 6.58
CHEMBL4873104 IC50 = 260.0 nM 6.58
CHEMBL4846921 IC50 = 260.0 nM 6.58