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24α-methyl Cholesterol Sale

(Synonyms: 菜油甾醇; (24R)-5-Ergosten-3β-ol) 目录号 : GC13431

A phytosterol

24α-methyl Cholesterol Chemical Structure

Cas No.:474-62-4

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1mg
¥410.00
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5mg
¥1,365.00
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Sample solution is provided at 25 µL, 10mM.

Description

24α-methyl Cholesterol is an agonist of liver X receptors (LXR).

Liver X receptors (LXRs) are ligand-dependent transcription factors involved in the transcriptional control of lipid metabolism. LXRs function as nuclear cholesterol sensors that are activated by elevated intracellular cholesterol levels in multiple cell types. Activation of LXRs induces the expression of various genes involved in cholesterol absorption, transport, efflux, and excretion. In addition to their function in lipid metabolism, LXRs have also been found to modulate immune and inflammatory responses in macrophages. LXRα is highly expressed in the liver and at lower levels in the adrenal glands, adipose, intestine, lung, macrophages, and kidney, and LXRβ is ubiquitously expressed [2].

24α-methyl Cholesterol was a phytosterol found in vegetables, nuts, fruits, and seeds that competitively inhibited the absorption of intestinal cholesterol and decreased the transcription of genes important for cholesterol metabolism [3]. 24α-methyl Cholesterol acted as an agonist at liver X receptors (LXR) and suppressed the proliferation of prostate and breast cancer cells [1].

References:
[1] Chuu C P, Kokontis J M, Hiipakka R A, et al.  Modulation of liver X receptor signaling as novel therapy for prostate cancer[J]. Journal of biomedical science, 2007, 14(5): 543-553.
[2] Zelcer N, Tontonoz P.  Liver X receptors as integrators of metabolic and inflammatory signaling[J]. The Journal of clinical investigation, 2006, 116(3): 607-614.
[3] Segura R, Javierre C, Lizarraga M A, et al.  Other relevant components of nuts: phytosterols, folate and minerals[J]. British Journal of Nutrition, 2006, 96(S2): S36-S44.

实验参考方法

Cell experiment:

The effect of campesterol on the viable cell number was assessed by XTT assay. HUVECs were treated with various concentrations (10, 20, 30, 40 and 50 μg/mL) of campesterol and incubated at 37 °C in a humidified incubator for 24 h, a XTT working solution was added to each well. The cells were incubated at 37 °C for 2 h and the optical density was measured using a microplate reader at 450 nm[1].

References:

[1]. Choi JM, et al. Identification of campesterol from Chrysanthemum coronarium L. and its antiangiogenic activities. Phytother Res. 2007 Oct;21(10):954-9.

化学性质

Cas No. 474-62-4 SDF
别名 菜油甾醇; (24R)-5-Ergosten-3β-ol
化学名 (3β,24R)-ergost-5-en-3-ol
Canonical SMILES O[C@H](C1)CC[C@@]2(C)C1=CC[C@]3([H])[C@]2([H])CC[C@@]4(C)[C@@]3([H])CC[C@]4([H])[C@H](C)CC[C@@H](C)C(C)C
分子式 C28H48O 分子量 400.7
溶解度 ≤0.25mg/ml in ethanol; 1mg/ml in dimethyl formamide; 0.8mg/ml in Water (ultrasonic and warming and heat) 储存条件 Store at 2-8°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.4956 mL 12.4782 mL 24.9563 mL
5 mM 0.4991 mL 2.4956 mL 4.9913 mL
10 mM 0.2496 mL 1.2478 mL 2.4956 mL
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