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K6PC-5

K6PC-5

产品编号 T27710   CAS 756875-51-1
别名: K6PC5, K6PC 5

K6PC-5 is a ceramide derivative that acts as an activator of sphingosine kinase 1 (SPHK1), inducing a swift and temporary rise in intracellular calcium levels. With its potential applications in skin diseases associated with abnormal keratinocyte function, as well as in studies on neurodegeneration and virus infection, K6PC-5 presents a promising compound for research purposes.

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K6PC-5 Chemical Structure
K6PC-5, CAS 756875-51-1
规格 价格/CNY 货期 数量
1 mg ¥ 347 现货
2 mg ¥ 490 现货
5 mg ¥ 828 现货
10 mg ¥ 1,230 现货
25 mg ¥ 2,480 现货
50 mg ¥ 3,480 现货
100 mg ¥ 4,870 现货
500 mg ¥ 9,830 现货
1 mL * 10 mM (in DMSO) ¥ 892 现货
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
重组蛋白限时优惠
Doxorubicin hydrochloride限时半价
产品目录号及名称: K6PC-5 (T27710)
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纯度: 98.55%
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生物活性
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存储 & 溶解度
参考文献
产品描述 K6PC-5 is a ceramide derivative that acts as an activator of sphingosine kinase 1 (SPHK1), inducing a swift and temporary rise in intracellular calcium levels. With its potential applications in skin diseases associated with abnormal keratinocyte function, as well as in studies on neurodegeneration and virus infection, K6PC-5 presents a promising compound for research purposes.
体外活性 K6PC-5 (1-10 μM; 24 h) increases the involucrin and loricrin levels in a dose-dependent manner in normal human epidermal keratinocytes (NHEKs). K6PC-5 promotes differentiation and proliferation of keratinocytes via intracellular Ca2+ signaling. In addition, K6PC-5 stimulates the phosphorylation of p42/44 extracellular signal-regulated kinase and c-Jun N-terminal kinase[1]. K6PC-5 (1-10 μM; 24 h) promotes fibroblasts proliferation and collagen synthesis in human fibroblasts. K6PC-5 induces intracellular Ca2+ concentration ([Ca2+]i) oscillations in human fibroblasts[2]. K6PC-5 (10, 25, and 50 μM; 48 h) significantly attenuates EBOV-induced infection in EBOV-infected EA.hy926 cells. K6PC-5 significantly reduces the virus titers in supernatants of infected cells and strikingly decreased the amount of VP40 in a concentration-dependent manner[3].
体内活性 在本质上老化的无毛小鼠(56周岁)中,1%的K6PC-5被局部应用2周。这种K6PC-5处理显著增加了真皮成纤维细胞的数量和胶原蛋白的产生。因此,真皮厚度也显著增加[2]。
别名 K6PC5, K6PC 5
分子量 343.5
分子式 C19H37NO4
CAS No. 756875-51-1

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

DMSO: 90 mg/mL (262 mM), Sonication is recommended.

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.9112 mL 14.556 mL 29.1121 mL 72.7802 mL
5 mM 0.5822 mL 2.9112 mL 5.8224 mL 14.556 mL
10 mM 0.2911 mL 1.4556 mL 2.9112 mL 7.278 mL
20 mM 0.1456 mL 0.7278 mL 1.4556 mL 3.639 mL
50 mM 0.0582 mL 0.2911 mL 0.5822 mL 1.4556 mL
100 mM 0.0291 mL 0.1456 mL 0.2911 mL 0.7278 mL

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TargetMol Library Books参考文献

1. Kwon YB, et al. Novel synthetic ceramide derivatives increase intracellular calcium levels and promote epidermal keratinocyte differentiation. J Lipid Res. 2007 Sep;48(9):1936-43. 2. Jong-Kyung Youm, et al. K6PC-5, a sphingosine kinase activator, induces anti-aging effects in intrinsically aged skin through intracellular Ca2+ signaling. J Dermatol Sci. 2008 Aug;51(2):89-102. 3. Imre G, et al. The sphingosine kinase 1 activator, K6PC-5, attenuates Ebola virus infection. iScience. 2021 Mar 5;24(4):102266. 4. Bernacchioni C, et al. The sphingosine kinase activator K6PC-5 stimulates C2C12 myoblast differentiation. Int J Immunopathol Pharmacol. 2011 Jan-Mar;24(1):55-62.
Ceranib-2 CS 2100 Etrasimod SKI V PF-543 Citrate Vibozilimod PF-543 hydrochloride Ozanimod

相关化合物库

该产品包含在如下化合物库中:
GPCR靶点分子库 膜蛋白靶向化合物库 经典已知活性库 已知活性化合物库

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母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。

体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

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您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。

Keywords

K6PC-5 756875-51-1 GPCR/G Protein S1P Receptor K6PC5 K6PC 5 Inhibitor inhibitor inhibit

 

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