1. Cell Cycle/DNA Damage Epigenetics Apoptosis
  2. HDAC Apoptosis
  3. HDAC-IN-46

HDAC-IN-46 (compound 12c) 是一种有效的 HDAC 抑制剂,对 HDAC1HDAC6IC50 分别为 0.21 μM 和 0.021 μM。HDAC-IN-46 在 MDA-MB-231 细胞中上调 p-p38,下调 Bcl-xL 和 cyclin D1。HDAC-IN-46诱导细胞周期 G2 期阻滞和细胞凋亡 (apoptosis)。HDAC-IN-46 可用于研究三阴性乳腺癌 (TNBC)。

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HDAC-IN-46 Chemical Structure

HDAC-IN-46 Chemical Structure

CAS No. : 2562386-85-8

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

HDAC-IN-46 (compound 12c) is a potent HDAC inhibitor with an IC50 value of 0.21 μM and 0.021 μM for HDAC1 and HDAC6, respectively. HDAC-IN-46 upregulates p-p38, and downregulates Bcl-xL and cyclin D1 in MDA-MB-231 cells. HDAC-IN-46 induces significant G2 phase arrest and apoptosis. HDAC-IN-46 can be used for researching triple-negative breast cancer (TNBC)[1].

IC50 & Target[1]

HDAC1

0.21 μM (IC50)

HDAC6

0.021 μM (IC50)

体外研究
(In Vitro)

HDAC-IN-46 (compound 12c) has antiproliferative activity against MDA-MB-231, A549 and MCF-7 with IC50s of 88.46±10.5 μM, 83.34 ± 15.5 μM and 21.4±3.7 μM, respectively[1].
HDAC-IN-46 (5, 12.5 and 25 μM; 24 h) causes concentration-dependent upregulation of p-p38 and downregulation of Bcl-xL and cyclin D1 in MDA-MB-231 cells[1].
HDAC-IN-46 (12.5 and 25 μM; 48 h) induces significant G2 phase arrest and apoptosis[1].

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

Western Blot Analysis[1]

Cell Line: MDA-MB-231 cells
Concentration: 5, 12.5 and 25 μM
Incubation Time: 24 h
Result: Caused concentration-dependent upregulation of p-p38 and downregulation of Bcl-xL and cyclin D1.

Cell Cycle Analysis[1]

Cell Line: MDA-MB-231 cells
Concentration: 12.5 and 25 μM
Incubation Time: 48 h
Result: Induced significant G2 phase arrest and apoptosis.
分子量

438.53

Formula

C22H30N8O2

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
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HDAC-IN-46
目录号:
HY-150597
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