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- MedChemExpress(MCE)
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- 2025年12月05日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
-20°C, sealed storage, away from moisture
- 英文名：
Mito-Lonidamine
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- 规格：
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥3703.0 |
|---|---|---|---|
| 规格： | 1 mg | 产品价格： | ￥1330.0 |
| 规格： | 5 mg | 产品价格： | ￥3500.0 |
| 规格： | 10 mg | 产品价格： | ￥4200.0 |
| 规格： | 25 mg | 产品价格： | ￥5880.0 |
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Mito-LND
CAS No. : 2361564-49-8
MCE 国际站：Mito-LND
产品活性：Mito-LND (Mito-Lonidamine) 是一种具有口服活性的且靶向线粒体的氧化磷酸化 (oxidative phosphorylation (OXPHOS)) 抑制剂。Mito-LND 抑制线粒体生物能，刺激活性氧 (reactive oxygen species) 的形成，并诱导肺癌细胞自噬细胞死亡。
研究领域：Metabolic Enzyme/Protease | NF-κB | Immunology/Inflammation | Autophagy
作用靶点：Mitochondrial Metabolism | Reactive Oxygen Species | Autophagy
In Vitro: Mito-LND blocks lung cancer growth, migration, and invasion. Mito-LND inhibits cell growth of H2030BrM3 and A549 cells with IC50 values of 0.74 µM and 0.69 µM, respectively.
Mito-LND inhibits mitochondrial complex I and II activities with IC50 values of 1.2 µM and 2.4 µM, respectively in H2030BrM3 cells.
Mito-LND (1 µM) increases ROS generation in H2030BrM3 lung cancer cells. Mito-LND potently induces mitochondrial ROS generation in H2030BrM3 lung cancer cells.
Mito-LND (2 µM) decreases the levels of phosphorylated AKT. Mito-LND also decreases the phosphorylation of P70S6K and other energy-sensing proteins in both the parental and metastatic lung cancer cell lines, indicating that Mito-LND specifically downregulates mTOR signaling.
In Vivo: Mito-LND (7.5 µmol/kg; oral gavage; 5 days per week; for 3 consecutive weeks) treatment markedly enhanced potency against both lung cancer progression and metastasis.
Mito-LND also decreases the rate of growth of A549 tumor xenografts.
Mito-LND treatment shows a marked decrease in lung cancer brain metastasis in NOD/SCID mice bearing H2030BrM3 cells.
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文献和实验就如上新手进阶要点总结之后，笔者总结了一下免疫荧光需要特别关注的细节，以期作出更完美的图片效果。1、了解及预测蛋白的定位例如：下图使用肺动脉内皮细胞（ BPAE）观察线粒体的显色，采用 405nm，488nm，561nm 的激光，100x NA 1.49 的物镜对细胞内线粒体的分布进行简单的观察，此图可见，单纯的 mito-tracker 并不能清晰看见线粒体内部的结构和蛋白相关关系，因此，明确蛋白定位，根据所需分辨率选择显微镜、相应的荧光蛋白和探针非常重要。比如研究者应大致预测观察目标是存在
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重新生成的，但具体的机制尚不清楚。 当beclin-1被活化后，胞浆中先形成很多个membrane source（自噬体膜发生中心），在它们不断扩展的过程中（phagophore到autolysosome），VMP1蛋白由内质网和高尔基体转位到自噬体膜上（VMP1又叫TMEM49，已知唯一与自噬有关的跨膜蛋白），同时，MAP1-LC3由胞浆型（即LC3-I）转位到自噬体膜（即LC3-II），LC3这一转变过程可被Western Blot和荧光显微镜检测到，现已成为监测自噬
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