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Deferiprone (Synonyms: 去铁酮) 纯度: 99.52%
Deferiprone 是唯一口服有活性的铁螯合剂, 用于研究地中海贫血中的输血性铁过载。

Deferiprone Chemical Structure
CAS No. : 30652-11-0
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10 mM * 1 mL in DMSO | ¥550 | In-stock | |
500 mg | ¥500 | In-stock | |
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5 g | ¥700 | In-stock | |
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Deferiprone 相关产品
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生物活性 |
Deferiprone is the only orally active iron-chelating drug to be used therapeutically in conditions of transfusional iron overload. Target: Deferiprone is an orphan drug designed and developed primarily by academic initiatives for the treatment of iron overload in thalassaemia. Deferiprone has been used in several other iron or other metal imbalance conditions and has prospects of wider clinical applications. Deferiprone has high affinity for iron and interacts with almost all the iron pools at the molecular, cellular, tissue and organ levels. Doses of 50-120 mg/kg/day appear to be effective in bringing patients to negative iron balance. Deferiprone increases urinary iron excretion, which mainly depends on the iron load of patients and the dose of the drug. |
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Clinical Trial |
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分子量 |
139.15 |
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Formula |
C7H9NO2 |
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CAS 号 |
30652-11-0 |
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中文名称 |
去铁酮 |
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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:
H2O : 8.33 mg/mL (59.86 mM; Need ultrasonic) DMSO : 7.14 mg/mL (51.31 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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