SR-4370

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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。

SR-4370  纯度: 98.03%

SR-4370 是一种有效的 HDAC 抑制剂，对 HDAC1，HDAC2，HDAC3，HDAC8 和 HDAC6 的 IC50 值分别为 0.13 μM，0.58 μM，0.006 μM，2.3 μM 和 3.4 μM。

SR-4370

SR-4370 Chemical Structure

CAS No. : 1816294-67-3

规格 价格 是否有货 数量
Free Sample (0.1-0.5 mg)   Apply now  
10 mM * 1 mL in DMSO ￥1760 In-stock
5 mg ￥1600 In-stock
10 mg ￥2700 In-stock
50 mg ￥9500 In-stock
100 mg ￥15000 In-stock
200 mg   询价  
500 mg   询价  

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生物活性

SR-4370 is an inhibitor of HDAC, with IC50s of 0.13 μM, 0.58 μM, 0.006 μM, 2.3 μM, and 3.4 μM for HDAC1, HDAC2, HDAC3, HDAC8, and HDAC6, respectively.

IC50 & Target[1]

HDAC3

6 nM (IC50)

HDAC1

130 nM (IC50)

HDAC2

580 nM (IC50)

HDAC8

2300 nM (IC50)

HDAC6

3400 nM (IC50)

体外研究
(In Vitro)

SR-4370 is an inhibitor of HDAC, with IC50s of 0.13 μM, 0.58 μM, 0.006 μM, 2.3 μM, and 3.4 μM for HDAC1, HDAC2, HDAC3, HDAC8, and HDAC6, respectively. SR-4370 is cytotoxic to the breast cancer cells (MDA-MB-231), with an IC50 of 12.6 μM[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.
分子量

304.33

Formula

C17H18F2N2O
CAS 号

1816294-67-3
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
溶解性数据
In Vitro: 

DMSO : ≥ 150 mg/mL (492.89 mM)

* “≥” means soluble, but saturation unknown.

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 3.2859 mL 16.4295 mL 32.8591 mL
5 mM 0.6572 mL 3.2859 mL 6.5718 mL
10 mM 0.3286 mL 1.6430 mL 3.2859 mL

*

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。
储备液的保存方式和期限：-80°C, 6 months; -20°C, 1 month。-80°C 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。
参考文献

  • [1]. LIAO, Daiqing, et al. HDAC INHIBITOR COMPOUNDS AND METHODS OF TREATMENT. WO 2015153516 A1.

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