ID: ALA3707977
Type: Binding
Description: Kinase Inhibition Assay: The compound of Example 39, 2-(1H-indol-5-ylamino)-6-(2,4-difluorophenylsulfonyl)-8-methylpyrido[2,3-d]pyrimidin-7(8H)-one, was subjected to a kinase inhibition assay for the kinases. Compounds were tested in 5 dose IC50 mode with 10-fold serial dilution starting at 10 μM. Staurosporine, a known protein kinase inhibitor, was tested in 5-dose IC50 mode with 3-fold serial dilution starting at 20 μM. Reactions were carried out in 10 μM ATP. The results are shown in Table 5. The results show that the compound of Example 39 is a kinase inhibitor highly selective for the kinase Plk2.
Format: BAO_0000357
Organism: Homo sapiens
Target: Ribosomal protein S6 kinase alpha 1(ALA2553)
Document: ALA3639034
BindingDB Source: 6572
Bioactivity
Activity Types for Assay ALA3707977
IC50
Parent Molecular Weight | ALogP | Polar Surface Area |
---|---|---|
417.47 | 4.84 | 4.84 |
452.51 | 4.75 | 4.75 |