上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。
PD150606 纯度: 98.19%
PD 150606 是一个选择性的,有细胞渗透性的非肽 calpain 抑制剂,对 μ-calpains 和 m-calpains 作用的 Ki 分别为 0.21 μM 和 0.37 μM,有神经保护活性。
PD150606 Chemical Structure
CAS No. : 179528-45-1
规格 | 价格 | 是否有货 | 数量 |
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Free Sample (0.1-0.5 mg) | Apply now | ||
10 mM * 1 mL in DMSO | ¥726 | In-stock | |
5 mg | ¥660 | In-stock | |
10 mg | ¥1100 | In-stock | |
25 mg | ¥2300 | In-stock | |
50 mg | ¥4100 | In-stock | |
100 mg | ¥7400 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
* Please select Quantity before adding items.
PD150606 相关产品
•相关化合物库:
- Covalent Screening Library Plus
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生物活性 |
PD 150606 is a selective, cell-permeable non-peptide calpain inhibitor with Ki values of 0.21 μM and 0.37 μM for μ- and m-calpains respectively, which is neuroprotective[1]. |
IC50 & Target |
Ki: 0.21 μM (μ-calpains), 0.37 μM (m-calpains)[1] |
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体外研究 (In Vitro) |
PD150606 interacts with both calcium-binding domains (μ- and m-calpains) of Calpain[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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分子量 |
306.12 |
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Formula |
C9H7IO2S |
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CAS 号 |
179528-45-1 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) |
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溶解性数据 |
In Vitro:
DMSO : ≥ 28 mg/mL (91.47 mM) * “≥” means soluble, but saturation unknown. 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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