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SZL P1-41
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。
SZL P1-41图片
CAS NO:222716-34-9
包装与价格:
包装价格(元)
10mM (in 1mL DMSO)询价
5mg询价
10mg询价
25mg询价
50mg询价
100mg询价

SZL P1-41 是一种特异性 Skp2 抑制剂,与 Skp2 的 F-box 结构域结合以阻止 Skp1 结合和 Skp2 SCF 复合物的形成。 SZL P1-41 与 Skp2 缺乏一样,会增强 p27 介导的细胞凋亡/衰老,同时削弱 Akt 驱动的糖酵解。抗肿瘤活性。
Cas No.222716-34-9
化学名3-(benzo[d]thiazol-2-yl)-6-ethyl-7-hydroxy-8-(piperidin-1-ylmethyl)-4H-chromen-4-one
Canonical SMILESCCC1=CC(C(C(C2=NC3=CC=CC=C3S2)=CO4)=O)=C4C(CN5CCCCC5)=C1O
分子式C24H24N2O3S
分子量420.52
溶解度DMSO: 5 mg/mL (11.89 mM),DMF: 1 mg/ml,Ethanol: 0.3 mg/ml
储存条件Store at -20℃
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

SZL P1-41 is a specific Skp2 inhibitor, binds to the F-box domain of Skp2 to prevent Skp1 association and Skp2 SCF complex formation. SZL P1-41, like Skp2 deficiency, augments p27-mediated apoptosis/senescence, while it impairs Akt-driven glycolysis. Anti-tumor activities[1][2].

SZL P1-41 (5-20μM; 24 hours) induces endogenous p27 protein expression in PC3 cells and also induced expression of p21, another Skp2 substrate[1].

SZL P1-41 (40-80 mg/kg; i.p.) displays a potent effect on inhibiting prostate and lung tumor growth in Nude mice bearing A549 and PC3 tumor xenografts[1].

References:
[1]. Chan CH et al. Pharmacological inactivation of Skp2 SCF ubiquitin ligase restricts cancer stem cell traits and cancer progression. Cell. 2013 Aug 1;154(3):556-68.
[2]. Chan CH, et al. Skp2: a dream target in the coming age of cancer therapy. Cell Cycle. 2014;13(5):679-80.

 
 
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