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。
SNDX-5613 纯度: 98.59%
SNDX-5613 是一种有效的特异性 Menin-MLL 抑制剂,结合 Ki 为 0.149 nM,细胞实验中,抑制 Menin-MLL 的 IC50 为 10-20 nM。SNDX-5613 可用于 MLL 基因重排的急性白血病研究,包括急性淋巴细胞白血病 (ALL) 和急性髓细胞白血病 (AML)。
SNDX-5613 Chemical Structure
CAS No. : 2169919-21-3
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 | ¥2776 | In-stock | |
5 mg | ¥2000 | In-stock | |
10 mg | ¥3500 | In-stock | |
25 mg | ¥7000 | In-stock | |
50 mg | ¥11000 | In-stock | |
100 mg | 询价 | ||
200 mg | 询价 |
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SNDX-5613 相关产品
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生物活性 |
SNDX-5613 is a potent and specific Menin-MLL inhibitor with a binding Ki of 0.149 nM and a cell based IC50 of 10-20 nM. SNDX-5613 can be used for the research of MLL-rearranged (MLL-r) acute leukemias, including acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML)[1]. |
IC50 & Target |
Menin-MLL[1] |
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体内研究 (In Vivo) |
SNDX-5613 shows in vivo plasma IC50 of 53 nM. SNDX-5613 treatment provides significant survival benefit and leukemic control in aggressive MOLM-13 disseminated xenografts[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 |
630.82 |
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Formula |
C32H47FN6O4S |
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CAS 号 |
2169919-21-3 |
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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 : 41.67 mg/mL (66.06 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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