Halobetasol Propionate
CAS No. 66852-54-8
Halobetasol Propionate ( BMY-30056 | CGP-14458 | Ulobetasol propionate )
产品货号. M18974 CAS No. 66852-54-8
丙酸卤倍他索是卤倍他索的丙酸盐形式,卤倍他索是一种合成皮质类固醇,具有抗炎、止痒和血管收缩活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥116 | 有现货 |
|
| 10MG | ¥159 | 有现货 |
|
| 25MG | ¥253 | 有现货 |
|
| 50MG | ¥358 | 有现货 |
|
| 100MG | ¥523 | 有现货 |
|
| 200MG | ¥771 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥126 | 有现货 |
|
生物学信息
-
产品名称Halobetasol Propionate
-
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
-
产品简述丙酸卤倍他索是卤倍他索的丙酸盐形式,卤倍他索是一种合成皮质类固醇,具有抗炎、止痒和血管收缩活性。
-
产品描述Halobetasol Propionate 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.
-
体外实验——
-
体内实验——
-
同义词BMY-30056 | CGP-14458 | Ulobetasol propionate
-
通路GPCR/G Protein
-
靶点Histamine Receptor
-
受体PLA2
-
研究领域Others-Field
-
适应症——
化学信息
-
CAS Number66852-54-8
-
分子量484.96
-
分子式C25H31ClF2O5
-
纯度>98% (HPLC)
-
溶解度DMSO : ≥ 35 mg/mL; 72.17 mM
-
SMILESC(=O)(CC)O[C@@]1([C@H](C[C@H]2[C@@H]3C[C@@H](C4=CC(=O)C=C[C@@]4([C@]3([C@H](C[C@]12C)O)F)C)F)C)C(=O)CCl
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Mohandas S, et al. Indian J Dermatol Venereol Leprol, 2009, 75(2), 186-187.
产品手册
关联产品
-
MK-0249
MK-0249 是一种新型强效选择性组胺 H3 反向激动剂。
-
Meclizine dihydrochl...
Meclizine 是一种组胺 H1 受体拮抗剂,用于治疗恶心和晕动病,具有抗组胺、抗毒蕈碱和抗氧化磷酸化特性。
-
Astemizole
Astemizole (R 43512) 是一个长效的二代抗组胺活性分子,是常用的抗过敏活性分子,是组胺 H1 受体 (histamine H1-receptor) 的拮抗剂,IC50 值为 4 nM。Astemizole 同时还具有hERG K+ 通道的阻断活性,IC50 值为 0.9 nM。Astemizole 还具有抗胆碱能和止痒作用。
021-51111890
购物车()
sales@molnova.cn

