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Merck
CN
所有图片(1)

文件

400091

Sigma-Aldrich

缺氧诱导因子羟化酶抑制剂,DMOG

The HIF-Hydroxylase Inhibitor, DMOG, also referenced under CAS 89464-63-1, controls the biological activity of HIF-Hydroxylase. This small molecule/inhibitor is primarily used for Cell Structure applications.

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别名:
缺氧诱导因子(HIF)羟化酶抑制剂,DMOG, N-(甲氧基乙酰基)-甘氨酸甲酯,二甲基草酰甘氨酸,HIF脯氨酰羟化酶抑制剂I,HIF天冬氨酰β羟化酶抑制剂,HIF天冬氨酰β羟化酶抑制剂
经验公式(希尔记法):
C6H9NO5
CAS号:
分子量:
175.14
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77

质量水平

检测方案

≥98% (HPLC)

制造商/商品名称

Calbiochem®

储存条件

OK to freeze
desiccated (hygroscopic)

颜色

pink-white to peach-white

溶解性

DMSO: 50 mg/mL

运输

ambient

储存温度

2-8°C

InChI

1S/C6H9NO5/c1-11-4(8)3-7-5(9)6(10)12-2/h3H2,1-2H3,(H,7,9)

InChI key

BNJOZDZCRHCODO-UHFFFAOYSA-N

一般描述

一种可渗透细胞的2-OG(2-氧戊二酸酯)类似物,有望作为所有2-OG依赖性双加氧酶的竞争性抑制剂。通过抑制HIF-PH-(HIF-α-脯氨酰羟化酶)催化的ODD(氧依赖性降解域)脯氨酰羟化(分别为HIF-1α和HIF-2α中的Pro564和Pro530)和天冬氨酰/天冬氨酰β羟化酶催化的CAD Asp羟基化(分别为HIF-1α和HIF-2α中的Asn803和Asn851),有效上调常氧HIF-α转录活性(培养物中的有效浓度=1 mM),阻断pVHL(von Hippel-Lindau)泛素连接酶复合物介导的HIF-α降解,同时促进HIF CAD(COOH末端激活域)p300/CBP关联性。还证明,DMOG可增强鼠体内缺血模型肌肉组织中动脉结扎诱导的HIF-1α和FLK的上调(在11天内分别上调100%和40%;8 mg/0.5 ml/动物/腹膜内;q.o.d.)。

警告

毒性:标准处理(A)

重悬

复溶后,等分并冷冻保存(-20°C)。储备溶液在-20°C下可稳定保存至多3个月。

其他说明

Pollard, P.J., et al. 2008.Biochem.J.416, 387.
Chen, H., et al. 2006.Cancer Res.66, 9009.
Milkiewicz, M., et al. 2004.J. Physiol.560, 21.
Lando, D., et al. 2002.Science295, 858.
Jaakkola, P., et al. 2001.Science292, 468.

法律信息

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

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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