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Assay Detail

CHEMBL963394

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

Functional
Growth inhibition of human BxPC3 cells after 72 hrs by MTS assay
16
Total Activities
16
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type BXPC-3
Confidence 1 — Organism
Curated By Autocuration

Target

BXPC-3 (CHEMBL614530)
Type CELL-LINE
Organism Homo sapiens

Publication

From a natural product lead to the identification of potent and selective benzofuran-3-yl-(indol-3-yl)maleimides as glycogen synthase kinase 3beta inhibitors that suppress proliferation and survival of pancreatic cancer cells.
Gaisina IN, Gallier F, Ougolkov AV, Kim KH, Kurome T, Guo S, Holzle D, Luchini DN, Blond SY, Billadeau DD, Kozikowski AP.
J Med Chem (2009) 52 : 1853 -1863
PubMed 19338355 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 16 5.38 6.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL523435 1 6.05
CHEMBL489043 1 6.05
CHEMBL522760 1 6.00
CHEMBL483465 ELRAGLUSIB 2.0 1 6.00
CHEMBL489407 1 5.70
CHEMBL522590 1 5.30
CHEMBL482632 1 5.22
CHEMBL491859 1 5.16
CHEMBL259850 1 4.85
CHEMBL522751 1 4.48
CHEMBL490860 1 4.38
CHEMBL102714 SB-216763 1 -
CHEMBL489422 1 -
CHEMBL484685 1 -
CHEMBL483669 1 -
CHEMBL491647 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL523435 IC50 = 900.0 nM 6.05
CHEMBL489043 IC50 = 900.0 nM 6.05
CHEMBL522760 IC50 = 1000.0 nM 6.00
CHEMBL483465 ELRAGLUSIB IC50 = 1000.0 nM 6.00
CHEMBL489407 IC50 = 2000.0 nM 5.70
CHEMBL522590 IC50 = 5000.0 nM 5.30
CHEMBL482632 IC50 = 6000.0 nM 5.22
CHEMBL491859 IC50 = 7000.0 nM 5.16
CHEMBL259850 IC50 = 14000.0 nM 4.85
CHEMBL522751 IC50 = 33000.0 nM 4.48
CHEMBL490860 IC50 = 42000.0 nM 4.38
CHEMBL102714 SB-216763 IC50 - -
CHEMBL489422 IC50 - -
CHEMBL484685 IC50 > 50000.0 nM -
CHEMBL483669 IC50 > 50000.0 nM -
CHEMBL491647 IC50 > 50000.0 nM -