1. Cell Cycle/DNA Damage Epigenetics
  2. HDAC
  3. G194-0712

G194-0712 是一种选择性组蛋白去乙酰化酶 5 (HDAC5) 激活剂,其 EC50 为 7.96 μM,Kd 为 2.53 μM。G194-0712 可恢复 ACTN4-K417 的去乙酰化及核转位,并上调 CSTA 的表达水平。G194-0712 可加速慢性伤口模型中的伤口闭合,缩小伤口面积与上皮间隙。G194-0712 可用于慢性皮肤伤口的相关研究,如糖尿病伤口、缺血性伤口、放射性损伤伤口。

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G194-0712

G194-0712 Chemical Structure

CAS No. : 1029737-28-7

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

G194-0712 is a selective histone deacetylase 5 (HDAC5) activator with an EC50 of 7.96 μM and a Kd of 2.53 μM. G194-0712 restores ACTN4-K417 deacetylation and nuclear import, and increases CSTA expression. G194-0712 accelerates wound closure in chronic wound models, reducing wound area and epithelial gap. G194-0712 can be used for the research of chronic skin wounds, such as diabetic wounds, ischemic wounds, radiation injury wounds[1].

IC50 & Target[1]

HDAC5

7.96 μM (EC50)

HDAC5

2.53 μM (Kd)

体外研究
(In Vitro)

G194-0712 对 HDAC4、HDAC7 和 HDAC9 表现出的 EC50 值分别为 107.2、100.4 和 111.5 μM[1]

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

体内研究
(In Vivo)

G194-0712 (25 μM;局部给药) 可通过恢复 ACTN4-K417 的去乙酰化、核转运及 CSTA 的表达,缩小 C57BLKS/J-db/db 小鼠的创面面积并减少上皮间隙,进而加速糖尿病小鼠的创面愈合和 C57BL/6J 小鼠缺血性、放射性损伤伤口的愈合[1]

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

Animal Model: C57BLKS/J-db/db (male, 8 weeks old, chronic wound model); C57BL/6J mice (male, 8 weeks old)[1]
Dosage: 25 μM
Administration: Topical application
Result: Reinstated ACTN4-K417 deacetylation and nuclear import.
Increased CSTA expression and reduced wound area at PODs 5, 9, 14, and 18.
Decreased epithelial gap.
分子量

353.85

Formula

C20H20ClN3O

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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产品名称:
G194-0712
目录号:
HY-181126
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