货号:A723561
同义名:
MitoQ mesylate; MitoQ10 mesylate
Mitoquinone mesylate是一种TPP为基础的、靶向线粒体的抗氧化剂,旨在保护线粒体免受氧化损伤。


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| 描述 | Mitoquinone mesylate, a TPP-derived antioxidant, is specifically designed to target mitochondria for protection against oxidative stress[1]. Mitoquinone, also known as MitoQ, is a mitochondria-focused antioxidant. Optimal dosages for MitoQ and DecylTPP are determined from dose-response trials during 4-hour cold storage. Mitoquinone's protective effects against cold storage damage are initially assessed using MitoSOX Red, a dye that detects mitochondrial superoxide production. NRK cells under cold storage exhibit approximately a two-fold increase in fluorescence, indicating mitochondrial superoxide generation, compared to untreated cells. Mitoquinone significantly shields against cold storage-induced mitochondrial superoxide production, unlike DecylTPP, which fails to provide protection. Mitoquinone treatment substantially lowers mitochondrial superoxide generation, while kidneys treated with DecylTPP show similar mitochondrial superoxide levels to those subjected to cold storage alone[1]. |
| Concentration | Treated Time | Description | References | |
| Platelets | 5 μM | 10 minutes | To evaluate TRAP-6-induced platelet aggregation and P-selectin expression. Results showed that TRAP-6 (5 μM) significantly increased platelet aggregation (88% ± 4.74%), while MitoQ at 5 μM significantly reduced aggregation (58.3% ± 5.1%). TRAP-6-induced P-selectin expression was not affected by MitoQ. | Int J Mol Sci. 2020 Aug 27;21(17):6192. |
| 3T3-L1 adipocytes | 100 nM | 30 min | MitoQ attenuated malonic acid-induced Fgf21, UCP1 and Cidea gene upregulation, suggesting that malonic acid-induced upregulation of FGF21 signalling is partly dependent on malonate altering mitochondrial redox signalling. | Nat Commun. 2025 Jan 2;16(1):170. |
| A549 cells | 1 μM | 24 h | To detect the effect of MitoQ on DEP-induced ROS levels, results showed that MitoQ did not significantly reduce ROS levels. | Environ Pollut. 2022 Jul 15;305:119292. |
| Normal rat kidney (NRK) cells | 100 nM | 48 h | MitoQ scavenged mitochondrial superoxide and prevented the increased protein expression of PGC1α and CORE II following MnSOD knockdown. | Redox Biol. 2014 Jan 23;2:348-57. |
| hASCs | 1 µM | 48 h | Mitoquinone was used to reduce mitochondrial reactive oxygen species (mtROS) and evaluate its effect on IDO activity. Results showed that Mitoquinone significantly reduced the response of P5 hASCs to IFN-γ stimulation, but had a lesser effect on P12 hASCs. | Front Immunol. 2021 Mar 10;12:621744. |
| MLE12 cells | 500 nM | 30 min | To evaluate the role of Mitoquinone in CdCl2-induced pyroptosis in MLE12 cells, the results showed that Mitoquinone significantly reduced CdCl2-induced mitochondrial ROS and the expression of pyroptosis-related proteins. | Cell Commun Signal. 2024 Nov 26;22(1):566. |
| Normal rat kidney (NRK cells) | 100 nM | 48 h | Mitoquinone prevented the increase in mitochondrial superoxide and nitrotyrosine following MnSOD knockdown by scavenging mitochondrial superoxide. | Redox Biol. 2014 Jan 23;2:348-57. |
| Administration | Dosage | Frequency | Description | References | ||
| Mice | CdCl2-induced lung injury model | Intraperitoneal injection | 3 mg/kg | Once daily for 7 days | To evaluate CdCl2-induced lung injury and alveolar epithelial cell pyroptosis, the results showed that CdCl2 exposure significantly increased the lung tissue inflammation score and the expression of pyroptosis-related proteins. | Cell Commun Signal. 2024 Nov 26;22(1):566. |
| Rats | Cardiac metabolism model | Oral | 500 μM | Daily for 2 weeks | MitoQ treatment improved cardiac energetics during Na elevation, reduced lactate and alanine concentrations, and reversed the shift in redox balance. | Nat Commun. 2024 May 20;15(1):4277 |
| Rats | Maternal psychosocial stress model during pregnancy | Intravenous injection | 90 μg/kg | Single injection, lasting 5 days | To investigate the effects of MitoQ-NP on placental oxidative stress induced by maternal psychosocial stress and its impact on offspring behavior and neurobiology. Results showed that MitoQ-NP treatment reduced placental and maternal oxidative stress and prevented anxiety-like behavior and neurobiological changes in male offspring induced by prenatal stress. | Neurobiol Stress. 2020 Nov 29;13:100281 |
| Animal study | Mitoquinone administration markedly mitigates pancreatic edema and neutrophil infiltration. It also causes a dose-dependent rise in serum amylase, nearly doubling at the higher dosage. MitoQ treatment almost doubles lung MPO activity triggered by Caerulein, with a notable increase in serum IL-6 levels at a dosage of 10 mg/kg[2]. |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
1.47mL 0.29mL 0.15mL |
7.37mL 1.47mL 0.74mL |
14.73mL 2.95mL 1.47mL |
|
| CAS号 | 845959-50-4 |
| 分子式 | C38H47O7PS |
| 分子量 | 678.81 |
| SMILES Code | O=C(C(CCCCCCCCCC[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3)=C4C)C(OC)=C(OC)C4=O.CS(=O)([O-])=O |
| MDL No. | MFCD30747833 |
| 别名 | MitoQ mesylate; MitoQ10 mesylate; Mitoquinone (mesylate); Mitoubiquinone mesylate |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 6个月 Pure form Inert atmosphere, 2-8°C |
| 溶解方案 |
DMSO: 105 mg/mL(154.68 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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