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- 详细信息
- 文献和实验
- 技术资料
- CAS号:
1354707-41-7
- 规格:
1mg/1mLx10mM(inDMSO)/5mg/10mg/25mg/50mg/100mg/200mg
| 规格: | 1mg | 产品价格: | ¥242.0 |
|---|---|---|---|
| 规格: | 1mLx10mM(inDMSO) | 产品价格: | ¥582.0 |
| 规格: | 5mg | 产品价格: | ¥529.0 |
| 规格: | 10mg | 产品价格: | ¥856.0 |
| 规格: | 25mg | 产品价格: | ¥1720.0 |
| 规格: | 50mg | 产品价格: | ¥2784.0 |
| 规格: | 100mg | 产品价格: | ¥3968.0 |
| 规格: | 200mg | 产品价格: | ¥5488.0 |
Product Introduction
Bioactivity
| 名称 | Mitochonic acid 5 |
| 描述 | Mitochonic acid 5 (MA-5) is a derivative of the plant hormone indole-3-acetic acid. Mitochonic acid 5 binds mitochondria and ameliorates renal tubular and cardiac myocyte damage.It has been shown to improve survival of fibroblasts from patients with mitochondrial diseases. |
| 细胞实验 | TNFα was used to induce inflammatory injury in mouse microglial BV-2 cells with and without prior MA-5 treatment. Cellular apoptosis was assessed using the MTT and TUNEL assays. Mitochondrial functions were evaluated via mitochondrial membrane potential JC-1 staining, ROS flow cytometry analysis, mPTP opening assessment, and immunofluorescence of cyt-c. Mitophagy was examined using western blots and immunofluorescence. The pathways analysis was carried out using western blots and immunofluorescence with a pathway blocker[1]. |
| 体外活性 | 使用MA-5处理通过上调自噬作用减少了线粒体凋亡。提高的自噬作用降解了受损的线粒体,打断了线粒体凋亡,中和了ROS过度产生,并提高了细胞的能量产生。我们还发现MA-5通过MAPK-ERK-Yap信号通路调控自噬作用是受到Bnip3的控制。抑制该信号通路或降低Bnip3表达阻止了MA-5对线粒体稳态的有益效果,并增加了微胶质细胞凋亡[1]。 |
| 存储条件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | DMSO : 120 mg/mL (364.41 mM), Sonication is recommended. 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 3.3 mg/mL (10.02 mM), Sonication is recommended. |
| 关键字 | Mitochonic acid-5 | Mitochonic acid5 | Mitochonic acid 5 | MitochondrialMetabolism | Mitochondrial Metabolism | MA5 | MA 5 | Inhibitor | inhibit |
| 相关产品 | L-Histidine | Sodium Molybdate | (-)-Epigallocatechin Gallate | Ciprofloxacin monohydrochloride | Rotenone | Imeglimin hydrochloride | Phenoxyethanol | 4'-Hydroxychalcone | 1-Hexanol | Phosphocreatine disodium | 4-Pentenoic acid | Ciprofloxacin hydrochloride monohydrate |
| 相关库 | Lipid Metabolism Compound Library | Bioactive Compound Library | Bioactive Compounds Library Max | Metabolism Compound Library | Mitochondria-Targeted Compound Library | Fluorochemical Library | Anti-Aging Compound Library | Natural Product Library | Glycometabolism Compound Library | Cuproptosis Compound Library | Natural Product Library for HTS | Covalent Inhibitor Library |
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文献和实验为 D. C. Aldridgi等( 1971)在植物病菌 Lasi-odiplodia theobromae的培养液中所发现的植物生长抑制物质,在未成熟的菜豆种子、栗叶等一些高等植物中也含有此物质。具有脱落酸 12— 14的生长阻抑活性。在南瓜种子中有与其相近的化合物葫芦酸( cucurbic acid),具有类似的生长阻抑活性。
异柠檬酸 isocitric acid柠檬酸的异构体,虽然量少,但广泛存在于生物界。在落地生根属( Bryophyllum)等多汁植物的叶、或悬钩子类中特别多,生物能够利用的是 D型。是三羧酸循环中的一个成分。柠檬酸在鸟头酸酶的作用下可逆地生成异柠檬酸和顺鸟头酸。在异柠檬酸脱氢酶( EC1. 1. 1. 41)的作用下变成 a-酮戊二酸,在异柠檬酸裂合酶( isocitrate lyase, EC4. 1. 3. 1)的作用下变成琥珀酸与乙醛
CH2 ICOOH,亦称一碘醋酸。熔点 82— 83℃。具有按下列方式与带有 SH基的物质结合的性质。 因此以 -SH为活性基的酶,例如醇脱氢酶、琥珀酸脱氢酶、 3-磷酸甘油醛脱氢酶和象 CoA那样的作用与- SH有关系的物质,可被碘乙酸特异地且不可逆地抑制。因此这一化合物对于发酵、糖酵解、肌肉收缩等也显示强抑制作用。
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