
Visomitin
CAS No. 934826-68-3
Visomitin ( SKQ1 bromide | PDTP )
产品货号. M16686 CAS No. 934826-68-3
Visomitin (SKQ1 bromide, PDTP) 是一种线粒体靶向抗氧化剂,可降低跨膜电位和活性氧 (ROS) 的产生。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥348 | 有现货 |
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10MG | ¥551 | 有现货 |
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25MG | ¥1021 | 有现货 |
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50MG | ¥1677 | 有现货 |
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100MG | ¥2957 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Visomitin
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Visomitin (SKQ1 bromide, PDTP) 是一种线粒体靶向抗氧化剂,可降低跨膜电位和活性氧 (ROS) 的产生。
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产品描述Visomitin (SKQ1 bromide, PDTP) is a mitochondria-targeted antioxidant that decreases transmembrane potential and production of reactive oxygen species (ROS); prevents neuronal loss and synaptic damage in a rat model of spontaneous Alzheimer’s disease, slows development of age-related ocular pathologies in murine, porcine, bovine, and canine model systems.(In Vitro):Direct treatment of tumor infiltrating leukocytes with Visomitin (SkQ1) does not influence their cytotoxicity against Panc02 cells. While Visomitin does not affect viability of the cell lines, this drug at 500 nM concentration reduces heavily the proliferation of human PDAC cells.(In Vivo):Regarding systemic angiogenic factors, it is observed in serum of Pancreatic ductal adenocarcinoma (PDAC) bearing mice a decrease in KC in the group of continuous treatment with Visomitin (SkQ1). Treatment of the mice with Visomitin increases the level of VEGF molecules. The amount of MIP1a and prolactin is reduced in all Visomitin treatment groups or after the follow-up treatment, respectively. Also, an increase in the IL-6 and IL-13 amount is found in the Visomitin treated groups. TGF-b amount is decreased in the pretreatment setting. On the contrary, all schemes of the Visomitin treatment decrease the NKT cell percentage. The Visomitin treatment has prolonged the median survival of PDAC-bearing mice, but the difference does not reach the level of significance defined.
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体外实验Direct treatment of tumor infiltrating leukocytes with Visomitin (SkQ1) does not influence their cytotoxicity against Panc02 cells. While Visomitin does not affect viability of the cell lines, this drug at 500 nM concentration reduces heavily the proliferation of human PDAC cells.
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体内实验Regarding systemic angiogenic factors, it is observed in serum of Pancreatic ductal adenocarcinoma (PDAC) bearing mice a decrease in KC in the group of continuous treatment with Visomitin (SkQ1). Treatment of the mice with Visomitin increases the level of VEGF molecules. The amount of MIP1a and prolactin is reduced in all Visomitin treatment groups or after the follow-up treatment, respectively. Also, an increase in the IL-6 and IL-13 amount is found in the Visomitin treated groups. TGF-b amount is decreased in the pretreatment setting. On the contrary, all schemes of the Visomitin treatment decrease the NKT cell percentage. The Visomitin treatment has prolonged the median survival of PDAC-bearing mice, but the difference does not reach the level of significance defined.
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同义词SKQ1 bromide | PDTP
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通路Others
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靶点Other Targets
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受体Others
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研究领域Other Indications
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适应症Other Disease
化学信息
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CAS Number934826-68-3
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分子量617.61
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分子式C36H42BrO2P
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纯度>98% (HPLC)
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溶解度DMSO: ≥29 mg/mL ( < 1 mg/ml refers to the product slightly soluble or insoluble )
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SMILESCC1=C(C(=O)C(=CC1=O)CCCCCCCCCC[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)C.[Br-]
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化学全称(10-(4,5-dimethyl-3,6-dioxocyclohexa-1,4-dien-1-yl)decyl)triphenylphosphonium bromide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Novikova YP, et al. Biochemistry (Mosc). 2014 Oct;79(10):1101-10.
2. Stefanova NA, et al. Aging (Albany NY). 2016 Oct 6;8(11):2713-2733.
3. Skulachev VP, et al. Biochem Biophys Res Commun. 2013 Nov 15;441(2):275-9.
4. Brzheskiy VV, et al. Adv Ther. 2015 Dec;32(12):1263-79.
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