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目录:MedChemExpress LLC>>生化试剂>> alpha-Mangostin | MCE

alpha-Mangostin | MCE
  • alpha-Mangostin | MCE
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  • 品牌 MedChemExpress (MCE)
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更新时间:2023-06-08 11:35:07浏览次数:147评价

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CAS 6147-11-1 纯度 99.64%
分子量 410.46 分子式 C₂₄H₂₆O₆
供货周期 现货 规格 10 mg
货号 HY-N0328 应用领域 医疗卫生,化工,生物产业,制药/生物制药
alpha-Mangostin | MCEalpha-Mangostin (α-Mangostin) is a dietary xanthone with broad biological activities, such as antioxidant, anti-allergic, antiviral, antibacterial, anti-inflammatory and anticancer effects. It is an inhibitor of mutant IDH1 (<b>IDH1-R132H</b>) with a <b>K<sub>i</sub></b> of 2.85 μM.

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alpha-Mangostin

CAS No. : 6147-11-1

产品活性:alpha-Mangostin (α-Mangostin) is a dietary xanthone with broad biological activities, such as antioxidant, anti-allergic, antiviral, antibacterial, anti-inflammatory and anticancer effects. It is an inhibitor of mutant IDH1 (IDH1-R132H) with a Ki of 2.85 μM.

研究领域:Immunology/Inflammation  |  NF-κB  |  Metabolic Enzyme/Protease  |  Apoptosis  |  Anti-infection

作用靶点:Reactive Oxygen Species  |  Apoptosis  |  Bacterial  |  Fungal  |  Virus Protease

结构分类:酚类  |  多酚类  |  酚类  |  氧杂蒽酮

来源:植物  |  其他科

In Vitro: alpha-Mangostin (α-Mangostin) exhibits a selective inhibitory effect on IDH1-R132H, but not on IDH1. alpha-Mangostin (α-Mangostin) competitively inhibits the binding of alpha-mangostin (α-KG) to IDH1-R132H. The structure–relationship study reveals that alpha-Mangostin (α-Mangostin) exhibits the strongest core inhibitor structure. alpha-Mangostin (α-Mangostin) selectively promotes demethylation of 5-methylcytosine (5mC) and histone H3 trimethylated lysine residues in IDH1 (+/R132H) MCF10A cells. Cell proliferation significantly decreases in a dose-dependent manner in the cells treated with alpha-mangostin. Alpha-mangostin also increases the levels of Bax (pro-apoptotic), cleaved caspase-3, cleaved caspase-9 and cleaved-poly(ADP-ribose) polymerase (PARP). alpha-Mangostin (α-Mangostin) significantly inhibits light-induced degeneration of photoreceptors and 200 μM H2O2-induced apoptosis of RPE cells. 200 μM H2O2-induced generation of reactive oxygen species (ROS) and light-induced generation of malondialdehyde (MDA) are suppressed by alpha-Mangostin (α-Mangostin).

In Vivo: alpha-Mangostin (α-Mangostin) reduces risk of liver fibrosis through the decrease in p53 expression as compared to the TAA_DMSO treatment. The serum levels of the liver enzymes AST and ALT after treatment with α-mangostin decrease as compared to DMSO alone.

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