HDAC3/6-IN-2

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。

HDAC3/6-IN-2 

HDAC3/6-IN-2 (化合物 15) 是一种有效的 HDAC6HDAC3 抑制剂,其 IC50 的值分别为 0.368 和 0.635 μM。HDAC3/6-IN-2 具有抗肿瘤活性,诱导癌细胞凋亡。HDAC3/6-IN-2 降低了 HDAC6HDAC3 的水平,与乙酰化 H3 和 α- 微管蛋白上调相关

HDAC3/6-IN-2

HDAC3/6-IN-2 Chemical Structure

CAS No. : 2417510-17-7

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生物活性

HDAC3/6-IN-2 (compound 15) is a potent HDAC6 and HDAC3 inhibitor, with IC50 values of 0.368 and 0.635 μM, respectively. HDAC3/6-IN-2 shows antitumor activity, and induces cancer cell apoptosis. HDAC3/6-IN-2 decreases the levels of HDAC6 and HDAC3, associated with upregulation of acetylated H3 and α-tubulin[1].

IC50 & Target

HDAC6

0.368 μM (IC50)

HDAC3

0.635 μM (IC50)

HDAC1

2.512 μM (IC50)

HDAC2

4.830 μM (IC50)

分子量

822.09

Formula

C49H67N5O6

CAS 号

2417510-17-7

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.

参考文献
  • [1]. Huang M, Xie X, Gong P, et al. A 18β-glycyrrhetinic acid conjugate with Vorinostat degrades HDAC3 and HDAC6 with improved antitumor effects. Eur J Med Chem. 2020;188:111991.

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