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

CHEMBL5719316

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

Binding
Inhibition of AKT in Melphalan Resistant human RPMI-8226 cells assessed as reduction of cell growth incubated for 72 hrs by CellTiter 96 aqueous one solution cell proliferation assay
4
Total Activities
4
Compounds Tested
1
Activity Types
2
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type Melphalan-resistant RPMI-8226 cell
Confidence 5 — Multiple protein complex / RNA
Curated By Autocuration

Target

Serine/threonine-protein kinase AKT (CHEMBL2111353)
Type PROTEIN FAMILY
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 4 5.59 6.56

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
CHEMBL1186409 1 6.56
CHEMBL379218 1 5.81
CHEMBL494089 GSK-690693 1.0 1 5.00
CHEMBL595583 1 5.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1186409 IC50 = 277.0 nM 6.56
CHEMBL379218 IC50 = 1549.8 nM 5.81
CHEMBL494089 GSK-690693 IC50 = 10000.0 nM 5.00
CHEMBL595583 IC50 = 10000.0 nM 5.00