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Assay Detail

CHEMBL889567

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

Binding
Inhibition of PKCmu
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Expert

Target

Serine/threonine-protein kinase D1 (CHEMBL3863)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and biological evaluation of 4(5)-(6-alkylpyridin-2-yl)imidazoles as transforming growth factor-beta type 1 receptor kinase inhibitors.
Kim DK, Jang Y, Lee HS, Park HJ, Yoo J.
J Med Chem (2007) 50 : 3143 -3147
PubMed 17552507 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 6.00 6.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL387748 1 6.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL387748 IC50 = 1000.0 nM 6.00