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Merck
CN

SML1840

Sigma-Aldrich

YK-3-237

别名:

B-[2-methoxy-5-[(1E)-3-oxo-3-(3,4,5-trimethoxyphenyl)-1-propen-1-yl]phenyl]-boronic acid

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关于此项目

经验公式(希尔记法):
C19H21BO7
化学文摘社编号:
分子量:
372.18
UNSPSC代码:
12352200
NACRES:
NA.77
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方案

≥98% (HPLC)

质量水平

表单

powder

颜色

white to beige

溶解性

DMSO: 25 mg/mL, clear

储存温度

2-8°C

生化/生理作用

YK-3-237 is an activator of sirtuin-1 (SIRT1).
YK-3-237 is an activator of sirtuin-1 (SIRT1). YK-3-237 showed anti-proliferative activity toward triple-negative breast cancer, inducing G2/M cell cycle arrest and apoptosis. In a study on renal fibrosis, YK-3-237 caused enhanced expression of α-SMA and fibronectin, suggesting that long-term use of SIRT1 activators may increase the risk or progression of chronic kidney disease.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Yong Weon Yi et al.
Oncotarget, 4(7), 984-994 (2013-07-13)
Many types of mutations in tumor suppressor p53 are oncogenic through gain-of-function. Therefore, targeting mutant p53 (mtp53) is a promising therapeutic approach to fight against many types of cancers. We report here a small molecule compound YK-3-237 that reduces acetylation
Murugavel Ponnusamy et al.
The Journal of pharmacology and experimental therapeutics, 354(2), 142-151 (2015-05-30)
Although activation of sirtuin-1 (SIRT1) has been shown to protect the kidney from acute injury, its role in renal fibrosis remains controversial since both inhibition and activation of SIRT1 have been reported to attenuate renal fibrosis. To resolve this conflict

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