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Skp2 Inhibitor C1
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Skp2 Inhibitor C1图片
CAS NO:432001-69-9
规格:98%
分子量:465.34
包装与价格:
包装价格(元)
100mg电议
200mg电议
10mg电议
50mg电议

产品介绍
Skp2 Inhibitor C1(SKPin C1)是特异的Skp2介导的p27降解抑制剂。
CAS:432001-69-9
分子式:C18H13BrN2O4S2
分子量:465.34
纯度:98%
存储:Store at -20°C

Background:

Skp2 Inhibitor C1(SKPin C1) is a specific small molecule inhibitor of Skp2-mediated p27 degradation, selectively inhibited Skp2-mediated p27 degradation by reducing p27 binding through key compound-receptor contacts.IC50 value: Target: Skp2 inhibitor; p27 regulatorin vitro: T47D cells treated with C1 (5 μM for 16 hours) displayedan increase in G1 phase (p< 0.0001) and a decrease in S phase (p< 0.0001), correlating with p27 protein induction. In contrast, MCF-7 cells responded to C1 with a significant reduction in G1 phase (35%, p< 0.0001) and an increase in G2-M phase (43%, p< 0.0001). This G1 reduction and G2/M arrest is dose dependent on C1 (Figure 5C right; p< 0.001 and p< 0.01, respectively) and correlates with increased p27 protein levels (Figure 5E left, S4A top right) [1].




[1]. Wu L, et al. Specific small molecule inhibitors of Skp2-mediated p27 degradation. Chem Biol. 2012 Dec 21;19(12):1515-24. [2]. Pavlides SC, et al. Inhibitors of SCF-Skp2/Cks1 E3 ligase block estrogen-induced growth stimulation and degradation of nuclear p27kip1: therapeutic potential for endometrial cancer. Endocrinology. 2013 Nov;154(11):4030-45.