胆固醇-(25R)-5-烯-3β,27-二醇, GPR183 激动剂;肝 X 受体-α 激动剂;肝 X 受体-β 激动剂

LXR激动剂
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库存信息

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库存信息

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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
C130177-5mg
5mg 现货 Stock Image
C130177-10mg
10mg 现货 Stock Image
C130177-25mg
25mg 现货 Stock Image

基本描述

别名 27-羟基胆固醇 | 25(R)-27-羟基胆固醇 | (25R)-26-羟基胆固醇 | (25R)-胆甾-5-烯-3b | 26-二醇 | 27-羟基胆固醇(25R) | 胆甾-5-ene-3β,27-二醇 | 11081825(R)-27-羟基胆固醇
英文别名 27-OHC | (25R) | 110818 | Cholest-5-ene-3-b,27-diol | PD018880 | CHOLEST-5-ENE-3.BETA.,26-DIOL, (25R)- | EX-A7666 | (25R)-26-Hydroxycholesterol | 26-HYDROXYCHOLESTEROL, (25R)- | Cholest-5-ene-3-beta,27-diol | Cholest-5-ene-3beta,27-diol | LMST01010088 | C
规格或纯度 Moligand™, ≥99%
英文名称 cholest-(25R)-5-ene-3β,27-diol
生化机理 LXR激动剂。雌激素受体部分激动剂。\ xa0调节乳腺癌细胞系中的基因表达。
应用 An oxysterol with cholesterol oxidation metabolite properties.
储存温度 -20°C储存
运输条件 超低温冰袋运输
作用类型 激动剂
作用机制 GPR183 激动剂;肝 X 受体-α 激动剂;肝 X 受体-β 激动剂
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产品介绍

27-羟基胆固醇(27-HC)是由胆固醇在肝脏中的甾醇27-羟化酶作用下合成的。在0.15至0.73 μM的循环范围中,它是一种丰富的氧化甾醇。27-HC是胆汁合成的底物

应用:

观察其对肝脏脂质积累的抑制作用;作为乳腺癌细胞系中的肝X受体(LXR)配体;作为液相色谱-串联质谱(LC-MS-MS)法中的对照,量化空肠样品中的25-OHC  

27-hydroxycholesterol (27-HC) is synthesized by cholesterol under the action of sterol 27-hydroxylase in the liver. It is an abundant oxidizing sterol in the cyclic range of 0.15 to 0.73 μM. 27-HC is a substrate for bile synthesis

Product description:

27-Hydroxycholesterol, an oxysterol secreted from macrophages, has been shown to be capable of passing through the blood-brain barrier and entering the circulation via the brain. This compound has been shown to be a cholesterol oxidation metabolite that causes an increase in levels of GADD 153 and caspase-12 in ARPE-19 cells in vitro. 27-Hydroxycholesterol has also been reported to increase levels of Aβ peptide production, reduce mitochondrial membrane potential, and induce nuclear factor κB (NFκB) and heme-oxygenase 1 (HO-1). Overall, 27-Hydroxycholesterol displays apoptotic properties via reactive oxygen species (ROS) generation, glutathione depletion, and inflammation. 27-Hydroxycholesterol is an activator of LXR α and LXR β.
An oxysterol with cholesterol oxidation metabolite properties.

Application:

To observe its inhibitory effect on lipid accumulation in liver. As a liver X receptor (LXR) ligand in breast cancer cell lines; As a control in liquid chromatography-tandem mass spectrometry (LC-MS-MS), 25-OHC in jejunum samples was quantified

AI解读

关联靶点(人)

NR1H2 Tchem 氧固醇受体 LXR-β(Oxysterols receptor LXR-beta) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
NR1H3 Tchem 氧固醇受体 LXR-alpha(Oxysterols receptor LXR-alpha) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
GPR183 Tchem G蛋白偶联受体183(G-protein coupled receptor 183) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
ABL1 Tclin Tyrosine-protein kinase ABL (18331 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GSK3B Tclin Glycogen synthase kinase-3 beta (11785 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CSNK1D Tchem Casein kinase I delta (4546 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NR1H3 Tchem LXR-alpha (2891 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CDK2 Tchem Cyclin-dependent kinase 2 (9050 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AURKA Tchem Serine/threonine-protein kinase Aurora-A (10240 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
U2OS (164939 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BRD4 Tchem Bromodomain-containing protein 4 (13122 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TRIM24 Tchem Transcription intermediary factor 1-alpha (2087 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BRPF1 Tchem Peregrin (2217 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

关联靶点(其它种属)

Mapk1 MAP kinase ERK2 (650 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Fgfr3 Fibroblast growth factor receptor 3 (21 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mycobacterium tuberculosis (203094 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Vero (26788 活性数据)
活性类型 Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

作用机制

作用机制 Action Type target ID Target Name Target Type Target Organism Binding Site Name 参考文献

名称和识别符

PubChem SID 504756957
分子类型 小分子
IUPAC Name (3S,8S,9S,10R,13R,14S,17R)-17-[(2R,6R)-7-hydroxy-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
INCHI InChI=1S/C27H46O2/c1-18(17-28)6-5-7-19(2)23-10-11-24-22-9-8-20-16-21(29)12-14-26(20,3)25(22)13-15-27(23,24)4/h8,18-19,21-25,28-29H,5-7,9-17H2,1-4H3/t18-,19-,21+,22+,23-,24+,25+,26+,27-/m1/s1
InChi Key FYHRJWMENCALJY-YSQMORBQSA-N
Canonical SMILES CC(CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)CO
Isomeric SMILES C[C@H](CCC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)O)C)C)CO
PubChem CID 123976
分子量 402.65

化学和物理性质

溶解性 ≤20mg/ml in ethanol;0.1mg/ml in DMSO;2mg/ml in dimethyl formamide
分子量 402.700 g/mol
XLogP3 7.100
氢键供体数Hydrogen Bond Donor Count 2
氢键受体数Hydrogen Bond Acceptor Count 2
可旋转键计数Rotatable Bond Count 6
精确质量Exact Mass 402.35 Da
单同位素质量Monoisotopic Mass 402.35 Da
拓扑极表面积Topological Polar Surface Area 40.500 Ų
重原子数Heavy Atom Count 29
形式电荷Formal Charge 0
复杂度Complexity 612.000
同位素原子数Isotope Atom Count 0
定义的原子立体中心计数Defined Atom Stereocenter Count 9
未定义的原子立体中心计数Undefined Atom Stereocenter Count 0
定义的键立体中心计数Defined Bond Stereocenter Count 0
未定义的键立体中心计数Undefined Bond Stereocenter Count 0
所有立体化学键的总数The total count of all stereochemical bonds 0
共价键合单元计数Covalently-Bonded Unit Count 1

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批号(Lot Number) 证书类型 日期 货号
K2328422 分析证书 23-11-16 C130177
K2328423 分析证书 23-11-16 C130177
K2328424 分析证书 23-11-16 C130177
K2328425 分析证书 23-11-16 C130177
K2328426 分析证书 23-11-16 C130177

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