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C4 Ceramide (d18:1/4:0)

C4 Ceramide (d18:1/4:0)

产品编号 T37564   CAS 74713-58-9
别名: C4 Ceramide (d18:1/4:0), Cer(d18:1/4:0)

C4 Ceramide is a bioactive sphingolipid and cell-permeable analog of naturally occurring ceramides. [1] [2] [3] It inhibits IL-4 production by 16% in EL4 T cells stimulated with phorbol 12-myristate 13-acetate when used at a concentration of 10 μM. [1] C4 Ceramide is cytotoxic to SK-BR-3 and MCF-7/Adr breast cancer cells (IC50s = 15.9 and 19.9 μM, respectively). [2] C4 Ceramide also increases maturation and stability of cystic fibrosis transmembrane conductance regulator (CFTR) proteins bearing the F508 deletion (F508del) mutation, enhances cAMP-activated chloride secretion, and suppresses secretion of IL-8 in primary epithelial cells isolated from patients with cystic fibrosis.[3]

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C4 Ceramide (d18:1/4:0) Chemical Structure
C4 Ceramide (d18:1/4:0), CAS 74713-58-9
规格 价格/CNY 货期 数量
10 mg ¥ 647 待询
50 mg ¥ 1,668 待询
100 mg ¥ 3,029 待询
药物设计专题培训
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
产品目录号及名称: C4 Ceramide (d18:1/4:0) (T37564)
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参考文献
产品描述 C4 Ceramide is a bioactive sphingolipid and cell-permeable analog of naturally occurring ceramides. [1] [2] [3] It inhibits IL-4 production by 16% in EL4 T cells stimulated with phorbol 12-myristate 13-acetate when used at a concentration of 10 μM. [1] C4 Ceramide is cytotoxic to SK-BR-3 and MCF-7/Adr breast cancer cells (IC50s = 15.9 and 19.9 μM, respectively). [2] C4 Ceramide also increases maturation and stability of cystic fibrosis transmembrane conductance regulator (CFTR) proteins bearing the F508 deletion (F508del) mutation, enhances cAMP-activated chloride secretion, and suppresses secretion of IL-8 in primary epithelial cells isolated from patients with cystic fibrosis.[3]
别名 C4 Ceramide (d18:1/4:0), Cer(d18:1/4:0)
分子量 369.58
分子式 C22H43NO3
CAS No. 74713-58-9

存储

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

溶解度

DMSO: 20 mg/mL

Ethanol: 30 mg/mL

DMF: 20 mg/mL

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TargetMol Library Books参考文献

1. Park, J., Li, Q., Chang, Y.T., et al. Inhibitory activity of a ceramide library in interleukin-4 production from activated T cells. Bioorg. Med. Chem. 13(7), 2589-2595 (2005). 2. Crawford, K.W., Bittman, R., Chun, J., et al. Novel ceramide analogues display selective cytotoxicity in drug-resistant breast tumor cell lines compared to normal breast epithelial cells. Cell Mol. Biol. (Noisy-le-grand) 49(7), 1017-1023 (2003). 3. Caohuy, H., Yang, Q., Eudy, Y., et al. Activation of 3-phosphoinositide-dependent kinase 1 (PDK1) and serum- and glucocorticoid-induced protein kinase 1 (SGK1) by short-chain sphingolipid C4-ceramide rescues the trafficking defect of ΔF508-cystic fibrosis transmembrane conductance regulator (ΔF508-CFTR). J. Biol. Chem. 289(52), 35953-35968 (2014).

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Keywords

C4 Ceramide (d18:1/4:0) 74713-58-9 d18:1/4:0 C-4 Ceramide (d18:1/4:0) Cer(d18:1/4:0) C4 Ceramide Inhibitor inhibitor inhibit

 

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