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Merck

700053P

Avanti

25-hydroxycholesterol-d6

Avanti Research - A Croda Brand

Sinónimos:

26,26,26,27,27,27-hexadeuterocholest-5-ene-3β,25-diol; 25-hydroxycholest-5-en-3-ol(d6)

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1 MG
MXP 7,927.00

MXP 7,927.00


Fecha estimada de envío14 de mayo de 2025


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1 MG
MXP 7,927.00

About This Item

Fórmula empírica (notación de Hill):
C27H40D6O2
Número de CAS:
Peso molecular:
408.69
Número MDL:
Código UNSPSC:
41141804
NACRES:
NA.25

MXP 7,927.00


Fecha estimada de envío14 de mayo de 2025


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descripción

cholest-5-ene-3β,25-diol-d6

Ensayo

>99% (TLC)

Formulario

powder

envase

pkg of 1 × 1 mg (700053P-1mg)

fabricante / nombre comercial

Avanti Research - A Croda Brand

Condiciones de envío

dry ice

temp. de almacenamiento

−20°C

Descripción general

25-hydroxycholesterol (25HC) is synthesized from cholesterol in the presence of oxygen and enzyme cholesterol 25-hydroxylase and the conversion is dependent on nicotinamide adenine dinucleotide phosphate (NADPH) during toll-like receptor activation. 25HC is catabolized to 7α-hydroxylated sterol.[1] 25-hydroxycholesterol-d6 is the deuterated form of 25-hydroxycholesterol.

Aplicación

25-hydroxycholesterol-d6 has been used as an internal standard:
  • in the quantification of 25-OHC in jejunum samples by liquid chromatography with tandem mass spectrometry (LC-MS-MS)[2]
  • in plasma samples by liquid chromatography-mass spectrometry analysis[3]
  • for calibration curve generation for plasma oxysterol quantification[4]

Acciones bioquímicas o fisiológicas

25-hydroxycholesterol is a liver X receptor ligand.[5] This bioactive lipid regulates immune response and macrophages production from monocytes.[1] 25-HC serves as an antiviral effector and may have therapeutic potential.[6] It reduces cholesterol biosynthesis by inactivating sterol regulatory element binding protein and inhibits HMG-CoA reductase (HMGCR).[6] 25-HC may play a protective role in myocardial ischemia-reperfusion injury by inhibiting apoptosis and regulating mitogen-activated protein kinase (MAPK) pathway.[5]

Envase

5 mL Amber Glass Screw Cap Vial (700053P-1mg)

Información legal

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Código de clase de almacenamiento

11 - Combustible Solids

Punto de inflamabilidad (°F)

No data available

Punto de inflamabilidad (°C)

No data available


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Elizabeth S Gold et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(29), 10666-10671 (2014-07-06)
Cross-talk between sterol regulatory pathways and inflammatory pathways has been demonstrated to significantly impact the development of both atherosclerosis and infectious disease. The oxysterol 25-hydroxycholesterol (25HC) plays multiple roles in lipid biosynthesis and immunity. We recently used a systems biology
Stian Solheim et al.
The Journal of steroid biochemistry and molecular biology, 192, 105309-105309 (2019-02-20)
Oxysterols can contribute to proliferation of breast cancer through activation of the Estrogen Receptors, and to metastasis through activation of the Liver X Receptors. Endogenous levels of both esterified and free sidechain-hydroxylated oxysterols were examined in breast cancer tumours from
Editorial: 25-Hydroxycholesterol: a new life in immunology.
Jeffrey G McDonald et al.
Journal of leukocyte biology, 88(6), 1071-1072 (2010-12-03)
Pallavi Mukherjee et al.
Journal of lipid research, 58(8), 1636-1647 (2017-06-09)
Feeding LDL receptor (LDLR)-null mice a Western diet (WD) increased the expression of IFN-β in jejunum as determined by quantitative RT-PCR (RT-qPCR), immunohistochemistry (IHC), and ELISA (all P < 0.0001). WD also increased the expression of cholesterol 25-hydroxylase (CH25H) as
Ying Liu et al.
Journal of lipid research, 59(3), 439-451 (2018-01-05)
Cholesterol 25-hydroxylase (CH25H) catalyzes the production of 25-hydroxycholesterol (25-HC), an oxysterol that can play an important role in different biological processes. However, the mechanisms regulating CH25H expression have not been fully elucidated. In this study, we determined that CH25H is

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