Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6173 |
BI 2536
4-[[(7R)-8-环戊基-7-乙基-5,6,7,8-四氢-5-甲基-6-氧代-2-喋啶基]氨基]-3-甲氧基-N-(1-甲基-4-哌啶基)苯甲酰胺 |
Apoptosis; Epigenetic Reader Domain; PLK | Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic |
BI 2536 一种是PLK1和BRD4的双抑制剂,IC50分别为 0.83 和 25 nM。它抑制 IFNB 干扰素 β 基因转录。 | |||
T68463 |
BI-4834
|
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BI-4834 is a potent and selective Polo-like kinase 1 (PLK1) inhibitor. BI-4834 is also analogue (or Me-Too) of BI-2536. In vitro test shows that BI 4834 inhibits PLK1 with IC50=7.6 nm, but with higher selectivity over the related enzyme PLK3 (IC50 198.4 nm) as BI-2536. |