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Merck

H9384

Sigma-Aldrich

22 (R)-羟基胆固醇

≥98%

别名:

22α-羟基胆固醇, 5-胆甾烯-3β,22(R)-二醇, 5-胆甾烯3β,22[R]-二醇

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About This Item

经验公式(希尔记法):
C27H46O2
CAS号:
分子量:
402.65
MDL號碼:
分類程式碼代碼:
12352211
eCl@ss:
39023139
PubChem物質ID:
NACRES:
NA.77

品質等級

化驗

≥98%

形狀

powder

運輸包裝

ambient

儲存溫度

room temp

SMILES 字串

[H][C@@]12CC=C3C[C@@H](O)CC[C@]3(C)[C@@]1([H])CC[C@]4(C)[C@H](CC[C@@]24[H])[C@H](C)[C@H](O)CCC(C)C

InChI

1S/C27H46O2/c1-17(2)6-11-25(29)18(3)22-9-10-23-21-8-7-19-16-20(28)12-14-26(19,4)24(21)13-15-27(22,23)5/h7,17-18,20-25,28-29H,6,8-16H2,1-5H3/t18-,20-,21-,22+,23-,24-,25+,26-,27+/m0/s1

InChI 密鑰

RZPAXNJLEKLXNO-GFKLAVDKSA-N

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應用

使用22(R)-羟基胆固醇处理牛主动脉内皮细胞以研究其对自由基产生的影响 以及用于与脂肪酸代谢有关的研究。

生化/生理作用

22(R)-羟基胆固醇是从胆固醇合成孕烯醇酮途径中的一种中间体。据报道它具有神经保护特性并可保护神经元免受β-淀粉样蛋白诱导的细胞死亡。 22(R)-羟基胆固醇可作为肝X受体的配体,该受体可充当甾醇浓度的传感器并调节脂肪酸代谢。

準備報告

22(R)-羟基胆固醇在氯仿中可产生澄清无色的溶液。

相關產品

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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A Chawla et al.
Science (New York, N.Y.), 294(5548), 1866-1870 (2001-12-01)
Cholesterol, fatty acids, fat-soluble vitamins, and other lipids present in our diets are not only nutritionally important but serve as precursors for ligands that bind to receptors in the nucleus. To become biologically active, these lipids must first be absorbed
Lourdes Cruz-Garcia et al.
Comparative biochemistry and physiology. Part A, Molecular & integrative physiology, 160(2), 125-136 (2011-06-04)
The liver X receptor (LXR) has recently been described in salmonids. In mammals, this receptor is already known as a transcriptional factor that regulates diverse aspects of cholesterol, fatty acid and carbohydrate metabolism in various tissues, including muscle. Here we
Cynthia Hong et al.
Journal of lipid research, 52(3), 531-539 (2010-12-29)
Ligand activation of liver X receptors (LXRs) has been shown to impact both lipid metabolism and inflammation. One complicating factor in studies utilizing synthetic LXR agonists is the potential for pharmacologic and receptor-independent effects. Here, we describe an LXR gain-of-function
Kosuke Dodo et al.
Bioorganic & medicinal chemistry, 16(8), 4272-4285 (2008-03-18)
Liver X receptors (LXR), which were originally reported as oxysterol-activated nuclear receptors, were recently found to recognize glucose as a physiological ligand. On this basis, we have already developed novel LXR antagonists based upon alpha-glucosidase inhibitors derived from thalidomide. Here
I L M H Aye et al.
Placenta, 32(2), 183-191 (2011-01-07)
Oxygenated cholesterol metabolites known as oxysterols display potent biological activities ranging from regulation of lipid homeostasis to cytotoxicity. Oxysterols have previously been shown to inhibit the invasion of first trimester trophoblasts, an effect which involves activation of the nuclear liver

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