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Assay Detail

CHEMBL4381714

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

Functional
Antiproliferative activity against human U87 cells assessed as reduction in cell viability after 72 hrs by MTT assay
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type U-87MG ATCC
Confidence 1 — Organism
Curated By Autocuration

Target

U-87 MG (CHEMBL614247)
Type CELL-LINE
Organism Homo sapiens

Publication

Identification of Parthenolide Dimers as Activators of Pyruvate Kinase M2 in Xenografts of Glioblastoma Multiforme in Vivo.
Ding Y, Xue Q, Liu S, Hu K, Wang D, Wang T, Li Y, Guo H, Hao X, Ge W, Zhang Y, Li A, Li J, Chen Y, Zhang Q.
J Med Chem (2020) 63 : 1597 -1611
PubMed 31977207 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 5.18 6.82

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL359744 DOXORUBICIN HYDROCHLORIDE 4.0 1 6.82
CHEMBL4466655 1 5.52
CHEMBL4591115 1 5.51
CHEMBL4298697 1 5.36
CHEMBL4450269 1 5.04
CHEMBL4438521 1 4.97
CHEMBL4543609 1 4.89
CHEMBL4483778 1 4.82
CHEMBL4577179 1 4.79
CHEMBL1085588 1 4.06
CHEMBL4459552 1 -
CHEMBL4448585 1 -
CHEMBL4454912 1 -
CHEMBL4449654 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL359744 DOXORUBICIN HYDROCHLORIDE IC50 = 150.0 nM 6.82
CHEMBL4466655 IC50 = 3030.0 nM 5.52
CHEMBL4591115 IC50 = 3090.0 nM 5.51
CHEMBL4298697 IC50 = 4380.0 nM 5.36
CHEMBL4450269 IC50 = 9130.0 nM 5.04
CHEMBL4438521 IC50 = 10590.0 nM 4.97
CHEMBL4543609 IC50 = 12920.0 nM 4.89
CHEMBL4483778 IC50 = 15070.0 nM 4.82
CHEMBL4577179 IC50 = 16170.0 nM 4.79
CHEMBL1085588 IC50 = 86300.0 nM 4.06
CHEMBL4459552 IC50 > 50000.0 nM -
CHEMBL4448585 IC50 > 50000.0 nM -
CHEMBL4454912 IC50 > 50000.0 nM -
CHEMBL4449654 IC50 > 50000.0 nM -