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Key Documents

700052P

Avanti

22(R)-hydroxycholesterol-d7

Avanti Research - A Croda Brand

Sinônimo(s):

25,26,26,26,27,27,27-heptadeuterocholest-5-ene-3β,22R-diol

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About This Item

Fórmula empírica (Notação de Hill):
C27H39O2D7
Número CAS:
Peso molecular:
409.70
Código UNSPSC:
41141804
NACRES:
NA.25

descrição

cholest-5-ene-3β,22(R)-diol-d7

Ensaio

>99% (TLC)

forma

powder

embalagem

pkg of 1 × 1 mg (700052P-1mg)

fabricante/nome comercial

Avanti Research - A Croda Brand

aplicação(ões)

lipidomics
metabolomics

Condições de expedição

dry ice

temperatura de armazenamento

−20°C

Descrição geral

22(R)-hydroxycholesterol is a diastereomer of 22(S)-hydroxycholesterol. It is present in the neonate brain. 22(R)-hydroxycholesterol-d7 is a deuterated form of 22(R)-hydroxycholesterol.

Ações bioquímicas/fisiológicas

22(R)-hydroxycholesterol (22(R)-HC) is a liver X receptor (LXR) ligand and is a key for the receptor activation.. 22(R)-HC promotes mesenchymal stem cell osteogenesis along with other oxysterols. It also regulates cholesterol homeostasis and suppresses prostate tumor progression. Low levels of 22(R)-HC is observed in Alzheimer′s disease and may be implicated in neuroinflammation and neurodegenerative diseases.

Embalagem

5 mL Amber Glass Screw Cap Vial (700052P-1mg)

Informações legais

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Código de classe de armazenamento

11 - Combustible Solids


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The Plant journal : for cell and molecular biology, 82(6), 991-1003 (2015-05-06)
Steroid alkaloids have been shown to elicit a wide range of pharmacological effects that include anticancer and antifungal activities. Understanding the biosynthesis of these molecules is essential to bioengineering for sustainable production. Herein, we investigate the biosynthetic pathway to cyclopamine
Chih-Pin Chuu et al.
Anticancer research, 30(9), 3643-3648 (2010-10-15)
Previously, we and other groups reported that liver X receptor (LXR) agonists T0901317, 22(R)-hydroxycholesterol, and 24(S)-hydroxycholesterol suppressed the proliferation of prostate and breast cancer cells. In this study, we report that T0901317 and 22(R)-hydroxycholesterol treatment inhibited the proliferation of different
Donglin Ma et al.
Biochimie, 103, 101-108 (2014-05-06)
Abnormal lipid metabolism may contribute to the pathogenesis of non-alcoholic steatohepatitis (NASH). The ATP-binding cassette transporter A1 (ABCA1) protein mediates the transport of cholesterol and phospholipids from cells to apolipoprotein A-I (apoA-I) to generate nascent HDL particles. Previous studies revealed

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