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经验公式（希尔记法）:
C27H39D7O2
化学文摘社编号:
分子量:
409.70
MDL number:
NACRES:
NA.25
UNSPSC Code:
12352100
产品名称
24(R/S)-hydroxycholesterol-d7, Avanti Research™ - A Croda Brand
description
cholest-5-ene-3β,24(R/S)-diol-d7
assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 1 mg (700018P-1mg)
pkg of 1 × 5 mg (700018P-5mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand
shipped in
dry ice
storage temp.
−20°C
Application
24(R/S)-hydroxycholesterol-d7 has been used as an internal standard in the quantification of sterols from biological samples by gas chromatography-mass spectrometry (GC–MS). It has also been used as an internal standard for the quantification of monohydroxycholesterols by MS analysis.
General description
24(R/S)-hydroxycholesterol-d7 is the deuterated form of 24(R/S)-hydroxycholesterol.
Packaging
5 mL Amber Glass Screw Cap Vial (700018P-1mg)
5 mL Amber Glass Screw Cap Vial (700018P-5mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
存储类别
11 - Combustible Solids
法规信息
美国出口管控产品
此项目有
William J Griffiths et al.
Free radical biology & medicine, 59, 69-84 (2012-08-01)
Bile acids, bile alcohols, and hormonal steroids represent the ultimate biologically active products of cholesterol metabolism in vertebrates. However, intermediates in their formation, including oxysterols and cholestenoic acids, also possess known, e.g., as ligands to nuclear and G-protein-coupled receptors, and
Andrea Civra et al.
The Journal of steroid biochemistry and molecular biology, 193, 105424-105424 (2019-07-16)
Oxysterols are cholesterol oxidation derivatives. Those containing an additional hydroxyl group on the side chain of the cholesterol molecule result from a physiological enzymatic synthesis and include the majority of oxysterols present in the circulation. Among these, 25-hydroxycholesterol (25OHC) and
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