
C16 Ceramide
CAS No. 24696-26-2
C16 Ceramide ( —— )
产品货号. M34959 CAS No. 24696-26-2
C16-Ceramide 是一种天然小分子,通过直接选择性结合激活 p53。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥315 | 有现货 |
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10MG | ¥476 | 有现货 |
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25MG | ¥931 | 有现货 |
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50MG | ¥1400 | 有现货 |
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100MG | ¥2050 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称C16 Ceramide
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述C16-Ceramide 是一种天然小分子,通过直接选择性结合激活 p53。
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产品描述C16-Ceramide is a natural small molecule activating p53 through the direct and selective binding.
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体外实验C16-Ceramide interacts with p53 within its core domain. p53 forms complex with natural C16-Ceramide in the cell.C16-Ceramide (2.5-50 μM; 0-48 h) strongly decreased HCT116 cell viability in a time- and concentration-dependent manner.C16-Ceramide (12 μM; 48 h) induces apoptosis through Btf (Bcl-2-associated transcription factor) in HCT116 cells.C16-ceramide (12 μM; 0-6 h) and Btf expression up-regulate p53 and BAX expression. C16-ceramide down-regulates Mdm2 expression via Btf.Cell Viability Assay Cell Line:HCT116 cells Concentration:2.5, 5, 10, 12, 20, 50 μM Incubation Time:0-48 h Result:Strongly decreased cell viability in a time- and concentration-dependent manner.Western Blot Analysis Cell Line:HCT116 cells Concentration:12 μM Incubation Time:1, 3 and 6 h Result:Increased PARP cleavage, decreased pro-caspase 3. Decreased the levels of stratifin and stathmin, increased the expression of prohibitin and Btf. RNAi-mediated Btf depletion also partially inhibited BAX expression after the treatment. Significantly decreased luciferase activity and Mdm2 protein expression levels.
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体内实验——
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同义词——
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通路Apoptosis
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靶点p53
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受体p53
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研究领域——
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适应症——
化学信息
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CAS Number24696-26-2
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分子量537.9
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分子式C34H67NO3
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纯度>98% (HPLC)
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溶解度In Vitro:?Ethanol 中的溶解度 : 20 mg/mL (37.18 mM; warming and heat to 60°C) DMF 中的溶解度 : 20 mg/mL (37.18 mM; 超声助溶 (<60°C))
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SMILESCCCCCCCCCCCCCCCC(=O)NC(CO)C(O)C=CCCCCCCCCCCCCC
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Fekry B, et al. C16-ceramide is a natural regulatory ligand of p53 in cellular stress response. Nat Commun. 2018 Oct 8;9(1):4149.?