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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 number:
NACRES:
NA.25
UNSPSC Code:
12352211
assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 1 mg (700029P-1mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand
shipped in
dry ice
storage temp.
−20°C
General description
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.
Application
3β,7β-dihydroxy-5-cholestenoic acid may be used as an authentic diastereoisomer standard in mass spectrometry (MS) experiments.
Biochem/physiol Actions
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.
Packaging
5 mL Amber Glass Screw Cap Vial (700029P-1mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
存储类别
11 - Combustible Solids
Metabolism of non-enzymatically derived oxysterols: clues from sterol metabolic disorders
Griffiths WJ, et al.
Free Radical Biology & Medicine, 144, 124-133 (2019)
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)
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