1. Cell Cycle/DNA Damage Epigenetics
  2. HDAC
  3. SE-7552

SE-7552 是 2-(difluoromethyl)-1,3,4-oxadiazole (DFMO) 衍生物,是一种具有口服活性的、高选择性、非异羟肟酸 HDAC6 抑制剂,IC50 为 33 nM。SE-7552 的选择性比所有其他已知的 HDAC 同工酶高 850 倍。SE-7552 能够阻断体内多发性骨髓瘤的生长。SE-7552 在饮食诱导的肥胖小鼠中充当抗肥胖剂。

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SE-7552 Chemical Structure

SE-7552 Chemical Structure

CAS No. : 2243575-79-1

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

SE-7552, a 2-(difluoromethyl)-1,3,4-oxadiazole (DFMO) derivative, is an orally active, highly selective, non-hydroxamate HDAC6 inhibitor with an IC50 of 33 nM. SE-7552 is greater than 850-fold selectivity versus all other known HDAC isozymes. SE-7552 is capable of blocking multiple myeloma growth in vivo. SE-7552 acts as an anti-obesity agent in diet-induced obese mice[1][2].

IC50 & Target[1]

HDAC6

33 nM (IC50)

体内研究
(In Vivo)

SE-7552 (30 mg/kg;单次口服灌胃) 可在小鼠体内增加乙酰化 α-微管蛋白水平超过 24 小时。SE-7552 对 H3 的乙酰化 (抑制 I 类 HDAC 的生物标志物) 没有影响[1]
SE-7552 (10 mg/kg;口服灌胃;每日) 与泊马度胺 (HY-10984;1 mg/kg;每日腹腔注射)联合使用,与单独泊马度胺组相比,在含有人 H929 MM 细胞的小鼠中可显着延迟肿瘤生长,并增强存活率[1]
SE-7552 表现出优异的 PK,小鼠单次口服剂量 5 mg/kg 后的最大暴露量为 597 ng/ml,半衰期为 7.2 小时[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

335.28

Formula

C15H12F3N5O

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献

SE-7552 相关分类

  • 摩尔计算器

  • 稀释计算器

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
SE-7552
目录号:
HY-161305
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