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HDACs/mTOR Inhibitor 1 纯度: 98.21%
HDACs/mTOR Inhibitor 1 是组蛋白去乙酰酶抑制剂 (HDAC) 和哺乳动物雷帕霉素 (mTOR) 的双重抑制剂,有潜力用于恶性血液病的研究,其对 HDAC1、HDAC6、mTOR 和 PI3Kα 的 IC50 值分别为 0.19 nM、1.8 nM、1.2 nM 和 >500 nM。HDACs/mTOR Inhibitor 1 能够引起 G0/G1 期的细胞阻滞,诱导肿瘤细胞凋亡,在体内毒性较低。
HDACs/mTOR Inhibitor 1 Chemical Structure
CAS No. : 2271413-06-8
规格 | 价格 | 是否有货 | 数量 |
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10 mM * 1 mL in DMSO | ¥5610 | In-stock | |
5 mg | ¥4500 | In-stock | |
10 mg | ¥7500 | In-stock | |
50 mg | ¥22500 | In-stock | |
100 mg | ¥33500 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
* Please select Quantity before adding items.
HDACs/mTOR Inhibitor 1 相关产品
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生物活性 |
HDACs/mTOR Inhibitor 1 is a dual Histone Deacetylases (HDACs) and mammalian target of Rapamycin (mTOR) target inhibitor for treating hematologic malignancies, with IC50s of 0.19 nM, 1.8 nM, 1.2 nM and >500 nM for HDAC1, HDAC6, mTOR and PI3Kα, respectively. HDACs/mTOR Inhibitor 1 stimulates cell cycle arrest in G0/G1 phase and induce tumor cell apoptosis with low toxicity in vivo[1]. |
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IC50 & Target |
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分子量 |
566.65 |
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Formula |
C28H38N8O5 |
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CAS 号 |
2271413-06-8 |
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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 : 32.5 mg/mL (57.35 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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