您的购物车当前为空
别名 卤倍他索丙酸酯, 卤贝他索丙酸酯, Ulobetasol propionate, Halobetasol Propionate, CGP-14458, BMY-30056
Halobetasol propionate (BMY-30056) 是一种在皮肤外使用的合成类固醇,具有抗炎,止痒和收缩血管的活性。


为众多的药物研发团队赋能,
让新药发现更简单!
Halobetasol propionate (BMY-30056) 是一种在皮肤外使用的合成类固醇,具有抗炎,止痒和收缩血管的活性。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 5 mg | ¥ 122 | 待询 | |
| 10 mg | ¥ 167 | 待询 | |
| 25 mg | ¥ 272 | 待询 | |
| 50 mg | ¥ 385 | 待询 | |
| 100 mg | ¥ 581 | 待询 | |
| 200 mg | ¥ 857 | 待询 | |
| 1 mL x 10 mM (in DMSO) | ¥ 133 | 待询 |
| 产品描述 | Halobetasol propionate (BMY-30056) is the propionate salt form of halobetasol, a synthetic corticosteroid with anti-inflammatory, antipruritic, and vasoconstrictor activities. Halobetasol, a topical steroid, diffuses across cell membranes to interact with cytoplasmic corticosteroid receptors located in both the dermal and intradermal cells, thereby activating gene expression of anti-inflammatory proteins mediated via corticosteroid receptor response element. Specifically, this agent induces phospholipase A2 inhibitory proteins, which inhibit the release of arachidonic acid, thereby inhibiting the biosynthesis of potent mediators of inflammation, such as prostaglandins and leukotrienes. As a result, halobetasol reduces edema, erythema, and pruritus through its cutaneous effects on vascular dilation and permeability. |
| 体外活性 | Halobetasol propionate通过诱导磷脂酶A2抑制蛋白(统称为lipocortins)来发挥作用。这些蛋白质通过抑制其共同前体花生四烯酸的释放,控制了如前列腺素和白三烯这类强烈炎症介质的生物合成。花生四烯酸从膜磷脂质中通过磷脂酶A2释放。最初的相互作用是由于该化合物与细胞质糖皮质激素受体结合。结合受体后,新形成的受体-配体复合体转移到细胞核中,在目标基因的启动子区域的许多糖皮质激素反应元件(GRE)上结合。与DNA结合的受体然后与基本转录因子互动,从而增加特定目标基因表达。[1] |
| 别名 | 卤倍他索丙酸酯, 卤贝他索丙酸酯, Ulobetasol propionate, Halobetasol Propionate, CGP-14458, BMY-30056 |
| 分子量 | 484.96 |
| 分子式 | C25H31ClF2O5 |
| CAS No. | 66852-54-8 |
| Smiles | CCC(=O)O[C@@]1([C@@H](C)CC2C3C[C@H](F)C4=CC(=O)C=CC4(C)[C@@]3(F)C(O)CC12C)C(=O)CCl |
| 密度 | 1.31 g/cm3 |
| 颜色 | White |
| 物理性状 | Solid |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||||||||||||
| 溶解度信息 | H2O: < 1 mg/mL (insoluble or slightly soluble) Ethanol: 36 mg/mL (74.23 mM), Sonication is recommended. DMSO: 90 mg/mL (185.58 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||||||||||||
| 体内实验配方 | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 3.3 mg/mL (6.8 mM), Sonication is recommended. 请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。 | ||||||||||||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||||||||||||
Ethanol/DMSO
DMSO
| |||||||||||||||||||||||||||||||||||||||||
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
对于不同动物的给药剂量换算,您也可以参考 更多