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Assay Detail

CHEMBL5710048

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

Binding
Inhibition of SLC34A2-ROS1 fusion protein expressed in human HCC78 cells assessed as inhibition of phosphorylated ROS1 incubated for 1 hr by ELISA analysis
5
Total Activities
5
Compounds Tested
1
Activity Types
2
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HCC78
Confidence 7 — Homologous single protein target
Curated By Autocuration

Target

SLC34A2-ROS1 (CHEMBL4680045)
Type CHIMERIC PROTEIN
Organism Homo sapiens

Publication

PF-06463922 is a potent and selective next-generation ROS1/ALK inhibitor capable of blocking crizotinib-resistant ROS1 mutations.
Zou HY, Li Q, Engstrom LD, West M, Appleman V, Wong KA, McTigue M, Deng YL, Liu W, Brooun A, Timofeevski S, McDonnell SR, Jiang P, Falk MD, Lappin PB, Affolter T, Nichols T, Hu W, Lam J, Johnson TW, Smeal T, Charest A, Fantin VR.
Proc Natl Acad Sci U S A (2015) 112 : 3493 -3498
PubMed 25733882 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 8.00 9.72

Assay Parameters

Parameter Type Value Units Text
EFO_ID EFO_ID - EFO:0003060
EFO_TERM EFO_TERM - non-small cell lung carcinoma

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5712062 1 9.72
CHEMBL601719 CRIZOTINIB 4.0 1 7.29
CHEMBL1230609 FORETINIB 2.0 1 7.00
CHEMBL2403108 CERITINIB 4.0 1 -
CHEMBL1738797 ALECTINIB 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5712062 IC50 = 0.19 nM 9.72
CHEMBL601719 CRIZOTINIB IC50 = 51.0 nM 7.29
CHEMBL1230609 FORETINIB IC50 = 99.0 nM 7.00
CHEMBL2403108 CERITINIB IC50 > 1000.0 nM -
CHEMBL1738797 ALECTINIB IC50 > 1000.0 nM -