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Assay Detail

CHEMBL5719621

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

Binding
Inhibition of IGF1R in human U-266 cells assessed as reduction of cell growth incubated for 72 hrs by CellTiter 96 aqueous one solution cell proliferation assay
3
Total Activities
3
Compounds Tested
1
Activity Types
2
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type U-266
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Insulin-like growth factor 1 receptor (CHEMBL1957)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Small molecule inhibitor screen identifies synergistic activity of the bromodomain inhibitor CPI203 and bortezomib in drug resistant myeloma.
Siegel MB, Liu SQ, Davare MA, Spurgeon SE, Loriaux MM, Druker BJ, Scott EC, Tyner JW.
Oncotarget (2015) 6 : 18921 -18932
PubMed 26254279 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 5.13 5.37

Assay Parameters

Parameter Type Value Units Text
EFO_ID EFO_ID - EFO:0001378
EFO_TERM EFO_TERM - multiple myeloma

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL399021 1 5.37
CHEMBL464552 1 5.01
CHEMBL466397 1 5.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL399021 IC50 = 4240.6 nM 5.37
CHEMBL464552 IC50 = 9773.4 nM 5.01
CHEMBL466397 IC50 = 10000.0 nM 5.00