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文件

475838

Sigma-Aldrich

米非司酮

≥99% (titration), solid, progesterone and glucocorticoid receptor antagonist, Calbiochem®

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别名:
米非司酮
经验公式(希尔记法):
C29H35NO2
CAS号:
分子量:
429.59
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77

质量水平

检测方案

≥99% (titration)

形式

solid

制造商/商品名称

Calbiochem®

储存条件

OK to freeze
protect from light

杂质

≤0.1% Steroid substances

颜色

yellow

溶解性

ethanol: 10 mg/mL

运输

ambient

储存温度

2-8°C

InChI

1S/C29H35NO2/c1-5-15-29(32)16-14-26-24-12-8-20-17-22(31)11-13-23(20)27(24)25(18-28(26,29)2)19-6-9-21(10-7-19)30(3)4/h6-7,9-10,17,24-26,32H,8,11-14,16,18H2,1-4H3/t24-,25+,26-,28-,29-/m0/s1

InChI key

VKHAHZOOUSRJNA-GCNJZUOMSA-N

一般描述

一种可渗透细胞的合成类固醇,作为孕激素和糖皮质激素受体的有效拮抗剂。抑制P-糖蛋白(P-gp)功能并下调P-gp介导的抗药性。显示抗血管生成作用并抑制血管内皮生长因子(VEGF)的产生。调节小鼠子宫内膜中Fas和FasL的表达以及前列腺癌细胞中TRAIL的表达。作为一种抗氧化剂,可提供针对CA1锥体细胞中受控皮层撞击(CCI)的神经保护作用,以及对小鼠海马HT22细胞的Aβ-,H2O2-和谷氨酸诱导性的损伤的神经保护作用。
一种可透过细胞的合成类固醇,作为孕激素和糖皮质激素受体的有效拮抗剂。 据报告可抑制P-糖蛋白(P-gp)功能并下调P-gp介导的抗药性。还显示抗血管生成作用并抑制血管内皮生长因子(VEGF)的产生。显示调节小鼠子宫内膜中Fas和FasL的表达以及前列腺癌细胞中TRAIL的表达。作为一种抗氧化剂,据报告可提供针对CA1锥体细胞中受控皮层撞击(CCI)的神经保护作用,以及对小鼠海马HT22细胞的Aβ-,H2O2-和谷氨酸诱导性的损伤的神经保护作用。

生化/生理作用

主要靶标
孕激素和糖皮质激素受体
产物不与ATP竞争。
可逆:否
细胞可渗透性:具有

包装

用惰性气体包装

警告

毒性:致癌/致畸(D)

重悬

复溶后等分并冷冻保存(-20°C)。贮备液在-20°C下可稳定保存至多3个月。

其他说明

McCullers, D.L., et al. 2002.Neuroscience109, 219.
Sidell, N., et al. 2002.Ann.N. Y. Acad.Sci.955, 159.
Gao, F., et al. 2001.Acta Pharmacol.Sin.22, 524.
Hyder, S.M., et al. 2001.Int. J. Cancer92, 469.
Lam, F.C., et al. 2001.J. Neurochem.76, 1121.
Sridhar, S., et al. 2001.Cancer Res.61, 7179.
Behl, C., et al. 1997.Eur. J. Neurosci.9, 912.
Greb, R.R., et al. 1997.Hum.Reprod.12, 1280.
Gruol, D.J., et al. 1994.Cancer Res.54, 3088.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Health hazard

警示用语:

Danger

危险声明

危险分类

Repr. 1B

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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