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Merck
CN

700029P

Avanti

3β,7β-dihydroxy-5-cholestenoic acid

Avanti Research - A Croda Brand

别名:

(25R)-cholest-5-en-26-oic acid, 3β,7β-hydroxy

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关于此项目

经验公式(希尔记法):
C27H44O4
化学文摘社编号:
分子量:
432.64
MDL编号:
UNSPSC代码:
12352211
NACRES:
NA.25
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方案

>99% (TLC)

表单

powder

包装

pkg of 1 × 1 mg (700029P-1mg)

制造商/商品名称

Avanti Research - A Croda Brand

运输

dry ice

储存温度

−20°C

一般描述

3β,7β-dihydroxy-5-cholestenoic acid (3β,7β-diHCA) is associated with plasma and is a C27 acid. 3β,7β-diHCA is synthesized from 3β-hydroxy-7-oxocholest-5-en-(25R)26-oic acid (3βH,7O-CA) by the action of the enzyme hydroxysteroid 11-β dehydrogenase 1.

应用

3β,7β-dihydroxy-5-cholestenoic acid may be used as an authentic diastereoisomer standard in mass spectrometry (MS) experiments.

生化/生理作用

3β,7β-dihydroxy-5-cholestenoic acid (3β,7β-diHCA) levels are elevated in Niemann-Pick type C (NPC) disease and Niemann-Pick (NP) disease type B disorders. It elicits toxicity to oculomotor neurons.

包装

5 mL Amber Glass Screw Cap Vial (700029P-1mg)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

储存分类代码

11 - Combustible Solids


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Sterolomics in biology, biochemistry, medicine
Griffiths WJ and Wang Y
TrAC, Trends in Analytical Chemistry, 115280-115280 (2018)
Charge-tagging liquid chromatography-mass spectrometry methodology targeting oxysterol diastereoisomers
Griffiths WJ, et al.
Chemistry and Physics of Lipids, 207, 69-80 (2017)
Metabolism of non-enzymatically derived oxysterols: clues from sterol metabolic disorders
Griffiths WJ, et al.
Free Radical Biology & Medicine, 144, 124-133 (2019)

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