Oxy-16
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 1mg | ¥2498.00 | 10-15工作日发货 | |
| 5mg | ¥8865.00 | 10-15工作日发货 | |
| 10mg | ¥15720.00 | 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
Oxy-16 is an antagonist of hedgehog activity.
Naturally occurring oxysterols that are products of cholesterol oxidation can stimulate the hedgehog (Hh) signaling pathway related to cardiovascular disease and bone formation. Activation of Hh signaling modulates inflammatory responses to additional atherogenic factors including lesion-producing macrophages and enable osteoblast differentiation, which is dependent on the target cell.
In vitro: Oxysterols have been shown to be associated with immunosuppression, apoptosis, atherosclerosis, inflammation, and cholesterol turnover. Other studies aslo indicated that oxysterols were Hedgehog (Hh) signaling pathway activators and had potent osteoinductive properties. Oxy-16, an oxysterol, was identified as a cell permeable oxygenated derivative of cholesterol that might be the end product or intermediate of the cholesterol excretion pathways. Oxy-16 is currently used as a transport form for cholesterol across the blood brain barrier and membranes. The osteogenic differentiation caused by Oxy-16 was cinsidered to be mediated via a Wnt signaling-related, Dkk-1-inhibitable mechanism [1].
In vivo: Up to now, there is no animal in vivo data reported.
Clinical trial: So far, no clinical study has been conducted.
Reference:
[1] Amantea, C. M.,Kim, W.K.,Meliton, V., et al. Oxysterol-induced osteogenic differentiation of marrow stromal cells is regulated by Dkk-1 inhibitable and PI3-kinase mediated signaling. Journal of Cellular Biochemistry 105(2), 424-436 (2008).
产品性质
| 物理外观 | A crystalline solid |
| CAS号 | 596-94-1 |
| 分子式 | C27H46O3 |
| 分子量 | 418.7 |
| 小分子别名 | 20α,22R-Dihydroxycholesterol |
| 化学名称 | cholest-5-ene-3b,20,22R-triol |
| 溶解度 | ≤10mg/ml in ethanol;1.5mg/ml in DMSO;1.5mg/ml in dimethyl formamide |
| SMILES | CC(C)CC[C@H]([C@@](C)([C@@H](CC1)[C@@](C)(CC2)[C@@H]1[C@H]1C2[C@@](C)(CC[C@@H](C2)O)C2=CC1)O)O |
| 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 | 20α,22R-二羟基胆固醇是一种内源性代谢中间体。20α,22R-二羟基胆固醇参与类固醇的生物合成。 |



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