DL-threo-PPMP (hydrochloride)
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 25mg | ¥3119.00 | 10-15工作日发货 | |
| 50mg | ¥4439.00 | 10-15工作日发货 | |
| 100mg | ¥5040.00 | 10-15工作日发货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
DL-threo-PPMP (hydrochloride) is an inhibitor of glucosylceramide synthase [1].
Glucosylceramide synthase (GCS) is a pervasive enzyme inherent to intracellular ceramide metabolism. The enzyme has been involved in catalyzing the transfer of glucose to ceramide, which is the principle committed step in glycolipid biosynthesis. GCS has been involved in the cytotoxic response of cancer cells to chemotherapy. Glucosylceramide synthase-based sphingolipids have been identified as important mediators of a variety of cellular functions, including proliferation, differentiation, development, and cell-cell recognition [2].
DL-threo-PPMP was a ceramide analog. DL-threo-PPMP inhibited the activity of glucosylceramide synthase with an IC50 value between 2 and 20 μM. It has been used to study the role of glucosylceramide synthase in cell growth, apoptosis, and autophagy [1].
References:
[1] Lee L, Abe A, Shayman J A. Improved inhibitors of glucosylceramide synthase[J]. Journal of Biological Chemistry, 1999, 274(21): 14662-14669.
[2] Bleicher R J, Cabot M C. Glucosylceramide synthase and apoptosis[J]. Biochimica et biophysica Acta (BBA)-Molecular and Cell Biology of Lipids, 2002, 1585(2): 172-178.
产品性质
| 物理外观 | A crystalline solid |
| CAS号 | 139974-41-7 |
| 分子式 | C29H50N2O3·HCl |
| 分子量 | 511.2 |
| 化学名称 | rel-N-[(1R,2R)-2-hydroxy-1-(4-morpholinylmethyl)-2-phenylethyl]-hexadecanamide, monohydrochloride |
| 溶解度 | ≤10mg/ml in ethanol;20mg/ml in DMSO;5mg/ml in dimethyl formamide |
| SMILES | O=C(CCCCCCCCCCCCCCC)N[C@H](CN1CCOCC1)[C@H](O)C2=CC=CC=C2.Cl |
| 存储条件 | -20°C |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | DL-threo-PPMP 盐酸盐是恶性疟原虫的一种抑制剂。DL-threo-PPMP 盐酸盐通过与模拟鞘磷脂的底物结合,抑制鞘磷脂合成酶的活性。这种抑制作用会导致敏感的鞘磷脂合成酶(SSS)活性迅速下降,选择性地破坏宿主细胞胞质中相互连接的 TVM 管状网络,而且这种抑制作用还会阻碍鞘磷脂合成酶(SSS)的增殖。 DL-threo-PPMP盐酸盐可用于研究疟疾生物学和寻找新的抗疟策略。 |



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