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SK1-I

    
≥98%

源叶(MedMol)
V46812 一键复制产品信息
1072443-89-0
C17H27NO2
277.40
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
V46812-1mg
≥98%

¥1590.00

货期:3-5天 - - - -
V46812-5mg
≥98%

¥3500.00

货期:3-5天 - - - -
V46812-10mg
≥98%

¥5800.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: SK1-I (BML-258), an analog of sphingosine, is an isozyme-specific competitive SPHK1 inhibitor with a Ki value of 10 μM. SK1-I shows no activity at SPHK1 PKCα, PKCδ, PKA, AKT1, ERK1, EGFR, CDK2, IKKβ or CamK2β. SK1-I enhances autophagy and has antitumor activity.
靶点: SphK1
体内研究: SK1-I (0-10 μM; 24 hours) attenuates cancer cell growth and survival in a TP53-dependent manner in HCT116 cells and HCT116 cells bearing TP53 null cancer.
SK1-I (0-20 μM; 12 hours) induces more CASP3 cleavage in HCT116 cells, compared to HCT116 cells lacking TP53, leading to a hallmark of apoptosis.
参考文献: 1. Melissa R Pitman, et al. Inhibitors of the sphingosine kinase pathway as potential therapeutics. Curr Cancer Drug Targets. 2010 Jun;10(4):354-67.
2. Santiago Lima, et al. TP53 is required for BECN1- and ATG5-dependent cell death induced by sphingosine kinase 1 inhibition. Autophagy. 2018;14(6):942-957.
3. Fiona H Greig, et al. Requirement for sphingosine kinase 1 in mediating phase 1 of the hypotensive response to anandamide in the anaesthetised mouse. Eur J Pharmacol. 2019 Jan 5;842:1-9.
 
保存条件: -20°C
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.605 ml 18.025 ml 36.049 ml
5 mM 0.721 ml 3.605 ml 7.21 ml
10 mM 0.36 ml 1.802 ml 3.605 ml
50 mM 0.072 ml 0.36 ml 0.721 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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