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动植物激素
Raloxifene HCl
| 品牌 | 厂商性质 | 产地 | 货期 |
|---|---|---|---|
| 阿拉丁 | 生产商 | 上海 | 现货 |
产品参数
| 货号 | CAS号 | 操作 |
|---|---|---|
| R129396-500mg | 82640-04-8 | 询底价 |
| R129396-25mg | 82640-04-8 | 询底价 |
| R129396-1g | 82640-04-8 | 询底价 |
| R129396-100mg | 82640-04-8 | 询底价 |
产品介绍
- 分子式 C28H27NO4S·HCl
- 分子量510.04
属性
| 溶解性 | Soluble in DMSO (50 mM), methanol, and ethanol (<1 mg/ml at 25 °C). Insoluble in water. |
| 存贮条件 | 储存温度-20°C |
描述
| 应用 | A SERM of ERα and ERβ. |
| 产品介绍 | Raloxifene HCl是estrogen（雌性激素）拮抗剂，抑制人体胞浆醛氧化酶催化的酞嗪氧化活性，IC50为5.7 nM。 |
| 备注 | Raloxifene is estrogen antagonists, inhibits human cytosolic aldehyde oxidase-catalyzed phthalazine oxidation activity with IC50 of 5.7 nM. |
| 生化机理 | Raloxifene hydrochloride is a selective estrogen receptor modulator (SERM), binding to ERα and ERβ. Tissue-dependently blocks or activates estrogen-induced transcription. Exhibits estrogen agonist behavior in bone but acts as an anti-estrogen in breast and uterine tissue. Raloxifene hydrochloride exhibits inhibitory effects of progesterone receptor induction by estrogen in D12 rat hypothalamic cells. Raloxifene hydrochloride is a substrate of Estrogen Receptor. |
| 别名 | 盐酸雷洛昔芬; [6-羟基-2-(4-羟苯基)苯并[b]噻酚-3-基]-[4-[2-(1-哌啶基)乙氧基]-苯基]-甲酮盐酸盐;Raloxifene Hydrochloride;keoxifene;[6-Hydroxy-2-(4-hydroxyphenyl)benzo[b]thien-3-yl][4-[2-(1-piperidinyl)ethoxy]phenyl]-methanone hydrochloride |
Raloxifene HCl信息由上海阿拉丁生化科技股份有限公司为您提供，如您想了解更多关于Raloxifene HCl报价、型号、参数等信息，欢迎来电或留言咨询。
注：该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案，不可用于临床诊断或治疗等相关用途