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Devimistat (Synonyms: CPI-613) 纯度: 99.59%
Devimistat (CPI-613) 是一种线粒体代谢抑制剂。Devimistat 是一种 lipoic acid拮抗剂,能阻断线粒体能量代谢,诱导多种癌细胞凋亡。
Devimistat Chemical Structure
CAS No. : 95809-78-2
规格 | 价格 | 是否有货 | 数量 |
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10 mM * 1 mL in DMSO | ¥770 | In-stock | |
5 mg | ¥700 | In-stock | |
10 mg | ¥880 | In-stock | |
50 mg | ¥2550 | In-stock | |
100 mg | ¥4350 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
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Devimistat 相关产品
•相关化合物库:
- Drug Repurposing Compound Library Plus
- Clinical Compound Library Plus
- Bioactive Compound Library Plus
- Apoptosis Compound Library
- Metabolism/Protease Compound Library
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- Neurodegenerative Disease-related Compound Library
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- Rare Diseases Drug Library
生物活性 |
Devimistat (CPI-613) is a mitochondrial metabolism inhibitor. Devimistat is a lipoic acid antagonist that abrogates mitochondrial energy metabolism to induce apoptosis in various cancer cells[1]. |
IC50 & Target |
mitochondrial metabolism[1] |
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体外研究 (In Vitro) |
Devimistat induces apoptosis of GPM-2 gastric cancer cells. Devimistat targets the altered form of mitochondrial energy metabolism utilized by tumor cells. The change in mitochondrial enzyme activities and cellular redox status induced by devimistat leads to cell death, including apoptosis[1]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only. |
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Clinical Trial |
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分子量 |
388.59 |
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Formula |
C22H28O2S2 |
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CAS 号 |
95809-78-2 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 100 mg/mL (257.34 mM; Need ultrasonic) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 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,建议您现用现配,当天使用; 以下溶剂前显示的百
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参考文献 |
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