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Meclizine dihydrochloride (NSC28728) 是一种组胺 H1 拮抗剂,用于治疗妊娠期间的晕动病、眩晕和恶心以及放射病。它是小鼠组成型雄甾烷受体激动剂,是人 CAR 的反向激动剂。它可透过血脑屏障,可用于多聚谷氨酰胺毒性障碍方面的研究。

Meclizine dihydrochloride (NSC28728) 是一种组胺 H1 拮抗剂,用于治疗妊娠期间的晕动病、眩晕和恶心以及放射病。它是小鼠组成型雄甾烷受体激动剂,是人 CAR 的反向激动剂。它可透过血脑屏障,可用于多聚谷氨酰胺毒性障碍方面的研究。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 50 mg | ¥ 298 | In stock | |
| 100 mg | ¥ 418 | In stock | |
| 5 g | ¥ 798 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 460 | In stock |
Meclizine dihydrochloride 相关产品
| 产品描述 | Meclizine dihydrochloride (NSC28728) is a histamine H1 antagonist used in the treatment of motion sickness, vertigo, and nausea during pregnancy and radiation sickness. |
| 体外活性 | Meclizine以CAR依赖的方式增加小鼠CAR靶基因的表达. |
| 体内活性 | Meclizine在体外实验中,剂量依赖性增加mCAR反式激活,激活激素受体共激活因子1与受体的结合。相反,Meclizine在来源于小鼠的只表达hCAR,不表达mCAR的肝脏细胞中,抑制hCAR转录激活和鲁米那诱导的CAR下游基因(包括细胞色素p450 单氧酶2B10、CYP3A11以及CYP1A2)的表达。Meclizine是小鼠CAR激动剂配体(组成型雄甾烷受体),人类CAR的反向激动剂。 |
| 细胞实验 | HepG2 cells are cultured in 24-well dishes with DMEM supplemented with 10% charcoal-stripped calf serum. Cells are transfected using calcium phosphate with 100 ng of receptor expression vectors, 300 ng of luciferase reporter plasmids, and 100 ng of pSV2-β-galactosidase as internal control of transfection efficiency. Drugs are added 12 h after transfection, and cells are incubated for an additional 24 h. The cell lysate is assayed for luciferase activity and normalized to β-galactosidase activity.(Only for Reference) |
| 别名 | 盐酸美克洛嗪, NSC28728, Meclozine dihydrochloride, Meclizine 2HCl |
| 分子量 | 463.87 |
| 分子式 | C25H27ClN2·2HCl |
| CAS No. | 1104-22-9 |
| Smiles | c1(cc(ccc1)C)CN1CCN(C(c2ccc(cc2)Cl)c2ccccc2)CC1.Cl.Cl |
| 密度 | 1.159g/cm3 |
| 存储 | keep away from moisture | 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 | DMSO: 15 mg/mL (32.34 mM), Sonication is recommended. | |||||||||||||||||||||||||
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DMSO
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