| CAS: | 138-14-7 | ||||||||||||
| 分子式: | C25H48N6O8.CH4O3S | ||||||||||||
| 分子量: | 656.79 | ||||||||||||
| 英文名称: |
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| 用途: | Deferoxamine mesylate is the mesylate salt of Deferoxamine, which forms iron complexes and is used as a chelating agent. |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||||||||||||||
| D875507 | MACKLIN | 甲磺酸去铁胺 | ≥92.5% | 128元/25mg; 358元/100mg; 966元/500mg; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
储存:-20℃ 状态:白色到灰白色粉末 | |||||||||||||||||||||||||||||||||||||||||||||||
| D873692 | MACKLIN | 甲磺酸去铁胺 | ≥98% | 58元/5mg; 185元/25mg; 395元/100mg; 1110元/500mg; 1619元/1g; 6599元/5g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
储存:-20℃ 状态:白色到灰白色固体 | |||||||||||||||||||||||||||||||||||||||||||||||
| 454081 | J&K | Deferoxamine mesylate salt | 97% | 465元/250MG; 1559元/1G; 5456元/5G; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
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| C46177 | Alfa Aesar | Deferoxamine mesylate | 95% | 4104元/1g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
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| 252750 | Millipore | Deferoxamine Mesylate-CAS 138-14-7-Calbiochem | Parenteral iron chelating agent. Commonly used in therapy as a chelator of ferric iron in disorders of iron overload. | 1877.44元/1 G; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 Parenteral iron chelating agent. Commonly used in therapy as a chelator of ferric iron in disorders of iron overload. Completely protects against dopamine-induced cell death. Has also been shown to interfere with hydroxyl radical formation, which mediates tissue damage in several disease states. Shows anti-proliferative effect on vascular smooth muscle cells in vitro and in vivo. Can also inhibit the oxidative chemistry of peroxynitrite by reaction of the hydroxamic acid moieties with trans-peroxynitrous acid. 包装 1 g in Plastic ampoule 警告 Toxicity: Harmful & Carcinogenic / Teratogenic (E) 其他说明 Bergeron, R.J., et al. 1996. J. Med. Chem. 39, 1575. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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| D9533 | Sigma-Aldrich | Deferoxamine mesylate salt | ≥92.5% (TLC), powder | 1649.92元/1 g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
产品说明 生化/生理作用 去铁胺被用作一个缺氧模拟物质去稳定低氧诱导因子1 (HIF-1)。 去铁胺通过抑制以HIF-1为靶点的脯氨酰羟化酶(PHDs)降解来稳定HIF-1。 去铁胺的抑制机制可能是通过Fe2+ 与酶活性所需的PHD活性位点的螯合作用而实现的。 基本信息
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| D0160000 | Deferoxamine mesylate salt | European Pharmacopoeia (EP) Reference Standard | 1572.27元/ ; | 展开 | |||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 本产品按照发行药典的发行和规定提供。支持本产品的所有信息,包括安全数据表和任何产品信息传单,都是在发行药典的授权下开发和发布的。 如需进一步信息和支持,请访问现行药典网站。 生化/生理作用 一种铁螯合剂,常用于研究细胞增殖和凋亡。 体外 和 体内 实验均显示其对血管平滑肌细胞具有抗增殖作用,并抑制G1期细胞的增殖。 据报道,它也诱导p53。 通过螯合铁诱导HL-60细胞凋亡。 经过1μM去铁胺处理48小时后,DNA明显断裂。 细胞经1μM去铁胺处理仅24小时后发生凋亡;48小时后观察到核坍塌。 一些研究表明,它具有抗氧化性能,并保护细胞免受H2O2诱导的损伤。 包装 单位数量:30 mg。随时可能改变。产品按照发行药典的规定交付。有关当前单位数量,请访问EDQM对照品目录。 注意 请参见 由EDQM提供的SDS。。 其他说明 可能适用相应的销售限制。 基本信息
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| Y0001934 | Deferoxamine for system suitability | European Pharmacopoeia (EP) Reference Standard | 1548.8元/ ; | 展开 | |||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia. 生化/生理作用 一种铁螯合剂,常用于研究细胞增殖和凋亡。 体外 和 体内 实验均显示其对血管平滑肌细胞具有抗增殖作用,并抑制G1期细胞的增殖。 据报道,它也诱导p53。 通过螯合铁诱导HL-60细胞凋亡。 经过1μM去铁胺处理48小时后,DNA明显断裂。 细胞经1μM去铁胺处理仅24小时后发生凋亡;48小时后观察到核坍塌。 一些研究表明,它具有抗氧化性能,并保护细胞免受H2O2诱导的损伤。 包装 Unit quantity: 15 mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue. 其他说明 Sales restrictions may apply. 基本信息
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| PHR3411 | Supelco | Deferoxamine mesylate | certified reference material, pharmaceutical secondary standard | 2000.81元/500 mg; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards 生化/生理作用 一种铁螯合剂,常用于研究细胞增殖和凋亡。 体外 和 体内 实验均显示其对血管平滑肌细胞具有抗增殖作用,并抑制G1期细胞的增殖。 据报道,它也诱导p53。 通过螯合铁诱导HL-60细胞凋亡。 经过1μM去铁胺处理48小时后,DNA明显断裂。 细胞经1μM去铁胺处理仅24小时后发生凋亡;48小时后观察到核坍塌。 一些研究表明,它具有抗氧化性能,并保护细胞免受H2O2诱导的损伤。 分析说明 These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available. 其他说明 This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis. 附注 To see an example of a Certificate of Analysis for this material enter LRAA6959(changes by product) in the Documents slot below. This is an example certificate only and may not be the lot that you receive. 基本信息
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| 1166003 | USP | Deferoxamine mesylate | United States Pharmacopeia (USP) Reference Standard | 3231.47元/300 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. 生化/生理作用 一种铁螯合剂,常用于研究细胞增殖和凋亡。 体外 和 体内 实验均显示其对血管平滑肌细胞具有抗增殖作用,并抑制G1期细胞的增殖。 据报道,它也诱导p53。 通过螯合铁诱导HL-60细胞凋亡。 经过1μM去铁胺处理48小时后,DNA明显断裂。 细胞经1μM去铁胺处理仅24小时后发生凋亡;48小时后观察到核坍塌。 一些研究表明,它具有抗氧化性能,并保护细胞免受H2O2诱导的损伤。 分析说明 These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind. 其他说明 USP issued SDS can be found here. 基本信息
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| BP987 | Desferrioxamine mesilate | British Pharmacopoeia (BP) Reference Standard | 1916.08元/30 MG; | 展开 | |||||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia. 生化/生理作用 一种铁螯合剂,常用于研究细胞增殖和凋亡。 体外 和 体内 实验均显示其对血管平滑肌细胞具有抗增殖作用,并抑制G1期细胞的增殖。 据报道,它也诱导p53。 通过螯合铁诱导HL-60细胞凋亡。 经过1μM去铁胺处理48小时后,DNA明显断裂。 细胞经1μM去铁胺处理仅24小时后发生凋亡;48小时后观察到核坍塌。 一些研究表明,它具有抗氧化性能,并保护细胞免受H2O2诱导的损伤。 包装 Unit quantity: 30 mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity please visit British Pharmacopoeia 其他说明 Sales restrictions may apply. 基本信息
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