AY 9944,99.71%

产品编号:Bellancom-107420| CAS NO:366-93-8| 分子式:C22H30Cl4N2| 分子量:464.30

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,

货号 包装 价格 库存与货期 购买量 操作
Bellancom-107420
1000.00 杭州 北京(现货)
Bellancom-107420
1700.00 杭州 北京(现货)
Bellancom-107420
3500.00 杭州 北京(现货)
Bellancom-107420
5500.00 杭州 北京(现货)
Bellancom-107420
8800.00 杭州 北京(现货)

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AY 9944

产品介绍 AY 9944 是一种特异的胆固醇生物合成 (cholesterol biosynthesis) 抑制剂。AY 9944 抑制 7- 脱氢胆固醇 Δ7- 还原酶 (DHCR7) 酶,其 IC50 值为 13 nM。AY 9944 引起胆固醇不足和 7DHC 积累。在高剂量下,AY 9944 也可在培养的胚胎中抑制固醇 Δ7-Δ8 异构酶,这会导致胆固醇 8-en-3β-ol 的积累。
生物活性

AY 9944 is a specific cholesterol biosynthesis inhibitor. AY 9944 inhibits the 7-dehydro cholesterol Δ7-reductase (DHCR7) enzyme with an IC50 of 13 nM. AY 9944 causes hypocholesterolemia and accumulation of 7DHC. At high doses, AY 9944 inhibits also in cultured embryos sterol Δ7-Δ8 isomerase, which causes the accumulation of cholest-8-en-3β-ol.

体外研究

AY 9944 (1 μg/mL; 15 h) affects types of free sterol in keratinocytes.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay

Cell Line: Human foreskin keratinocytes
Concentration: 1 μg/mL
Incubation Time: 15 hours
Result: Inhibited the synthesis of cholesterol and desmosterol, but increased 7-dehydrocholesterol and zymosterol synthesis.
体内研究
(In Vivo)

AY 9944 (7.5 mg/kg; i.h. every 6 days once from postnatal day 2 to postnatal day 20) reduces brain cholesterol until 400 days after stop treatment.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Long–Evans hooded rats.
Dosage: 7.5 mg/kg
Administration: Subcutaneous injection; 7.5 mg/kg every 6 days once; from postnatal day 2 to postnatal day 20
Result: Reduced brain cholesterol and increased 7-dehydrocholesterol in all brain regions of rats till the treatment stopped for 400 days and showed a more severe effect on the change of sterols in plasma and liver of female rats.
体内研究

AY 9944 (7.5 mg/kg; i.h. every 6 days once from postnatal day 2 to postnatal day 20) reduces brain cholesterol until 400 days after stop treatment.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Long–Evans hooded rats.
Dosage: 7.5 mg/kg
Administration: Subcutaneous injection; 7.5 mg/kg every 6 days once; from postnatal day 2 to postnatal day 20
Result: Reduced brain cholesterol and increased 7-dehydrocholesterol in all brain regions of rats till the treatment stopped for 400 days and showed a more severe effect on the change of sterols in plasma and liver of female rats.
体内研究

AY 9944 (7.5 mg/kg; i.h. every 6 days once from postnatal day 2 to postnatal day 20) reduces brain cholesterol until 400 days after stop treatment.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Long–Evans hooded rats.
Dosage: 7.5 mg/kg
Administration: Subcutaneous injection; 7.5 mg/kg every 6 days once; from postnatal day 2 to postnatal day 20
Result: Reduced brain cholesterol and increased 7-dehydrocholesterol in all brain regions of rats till the treatment stopped for 400 days and showed a more severe effect on the change of sterols in plasma and liver of female rats.
性状Solid
溶解性数据
In Vitro: 

DMSO : 5 mg/mL (10.77 mM; Need ultrasonic)

H2O : 5 mg/mL (10.77 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.1538 mL 10.7689 mL 21.5378 mL
5 mM 0.4308 mL 2.1538 mL 4.3076 mL
10 mM 0.2154 mL 1.0769 mL 2.1538 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

参考文献

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