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Assay Detail

CHEMBL3882685

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

Binding
Inhibition of PDGFRA in human PANC1 cells measured after 4 days by sulforhodamine B assay
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type PANC-1
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Platelet-derived growth factor receptor alpha (CHEMBL2007)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Substituted tricyclic compounds as protein kinase inhibitors
(2008)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 4.88 5.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2103851 AMUVATINIB 2.0 1 5.52
CHEMBL3914378 1 4.80
CHEMBL1642 IMATINIB MESYLATE 4.0 1 4.62
CHEMBL102301 1 4.58
CHEMBL3926830 1 -
CHEMBL3924103 1 -
CHEMBL3966621 1 -
CHEMBL3935261 1 -
CHEMBL456689 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2103851 AMUVATINIB IC50 = 3000.0 nM 5.52
CHEMBL3914378 IC50 = 16000.0 nM 4.80
CHEMBL1642 IMATINIB MESYLATE IC50 = 24000.0 nM 4.62
CHEMBL102301 IC50 = 26600.0 nM 4.58
CHEMBL3926830 IC50 > 50000.0 nM -
CHEMBL3924103 IC50 > 50000.0 nM -
CHEMBL3966621 IC50 > 50000.0 nM -
CHEMBL3935261 IC50 - -
CHEMBL456689 IC50 > 50000.0 nM -