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AR-42 (OSU-HDAC42)

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产品名称: AR-42 (OSU-HDAC42)
产品型号: GOY-Y1905
产品展商: 谷研
产品文档: 无相关文档
发布时间:2023-04-25

简单介绍

AR-42 (OSU-HDAC42)≥ 15.62 mg/mL in DMSO


AR-42 (OSU-HDAC42)  的详细介绍

性能参数

产品名称

AR-42 (OSU-HDAC42)

规格

10mM (in 1mL DMSO) 2mg 5mg 10mg 50mg

货号

GOY-Y1905

 含量

>98.00%

CAS

935881-37-1

别名

N/A

 

 

化学名

N-hydroxy-4-[[(2S)-3-methyl-2-phenylbutanoyl]amino]benzamide

分子式

C18H20N2O3

分子量

分子 312.36

溶解度

≥ 15.62 mg/mL in DMSO

储存条件

Store at -20°C

General tips

 

用途

仅供科研

价格

电询

详细内容

AR-42 (also known as OSU-HDAC42), a derivative of hydroxamate-tethered phenylbutyrate, is a novel and potent inhibitor of histone deacetylase (HDAC) that potently inhibits the activity of HDAC with 50% inhibition concentration IC50 value of 16 nM and induces histone H3 acetylation, α-tubulin acetylation and p21 up-regulation, which have been considered as the hallmark indicators of HDAC inhibition. AR-42 has been found to modulate several apoptosis inhibitors as well as cell survival regulator, including Akt, Bcl-xL, Bax, Ku70 and surviving, and exert potent antitumor activity against multiple tumor types, such as human prostate and hepatic cancers, at least partially through PI3K/Akt pathway inhibition.

Reference

[1].Matthew L. Bush?, Janet Oblinger?, Victoria Brendel, Griffin Santarelli, Jie Huang, Elena M. Akhmametyeva, Sarah S. Burns, Justin Wheeler, Jeremy Davis, Charles W. Yates, Abhik R. Chaudhury, Samuel Kulp, Ching-Shih Chen, Long-Sheng Chang, D. Bradley Welling, and Abraham Jacob. AR42, a novel histone deacetylase inhibitor, as a potential therapy for vestibular schwannomas and meningiomas. Neuro-Oncology 13(9):983–999, 2011

[2].Aaron M. Sargeant, Robert C. Rengel, Samuel K. Kulp, et al. OSU-HDAC42, a Histone Deacetylase Inhibitor, Blocks Prostate Tumor Progression in the Transgenic Adenocarcinoma of the Mouse Prostate Model Cancer Res 2008;68:3999-4009.

[3].Qiang Lu, Da-Sheng Wang, Chang-Shi Chen, Yuan-Dong Hu, and Ching-Shih Chen. Structure-Based Optimization of Phenylbutyrate-Derived Histone Deacetylase

[4].Inhibitors. J. Med. Chem. 2005, 48, 5530-5535

 

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