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Dihydrocoumarin (Hydrocoumarin)

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产品名称: Dihydrocoumarin (Hydrocoumarin)
产品型号: GOY-Y3435
产品展商: 谷研
产品文档: 无相关文档
发布时间:2023-05-08

简单介绍

Dihydrocoumarin (Hydrocoumarin)Insoluble in H2O; ≥42.2 mg/mL in EtOH; ≥73.6 mg/mL in DMSO


Dihydrocoumarin (Hydrocoumarin)  的详细介绍

性能参数

产品名称

Dihydrocoumarin (Hydrocoumarin)

规格

100mg

货号

GOY-Y3435

 含量

>98.00%

CAS

119-84-6

别名

N/A

 

 

化学名

N/A

分子式

C9H8O2

分子量

分子量 148.16

溶解度

Insoluble in H2O; ≥42.2 mg/mL in EtOH; ≥73.6 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

Dihydrocoumarin is a compound found in Melilotus officinalis. Dihydrocoumarin is a yeast Sir2p inhibitor. Dihydrocoumarin also inhibits human SIRT1 and SIRT2 with IC50s of 208 μM and 295 μM, respectively[1].

Dihydrocoumarin induces a concentration-dependent inhibition of SIRT1 (IC50 of 208 μM) in an in vitro enzymatic assay. A decrease in SIRT1 deacetylase activity is observed even at micromolar doses (85±5.8 and 73±13.7% activity at 1.6 μM and 8 μM, respectively). The microtubule SIRT2 deacetylase is also inhibited with a similar dose dependency (IC50 of 295 μM)[1].Dihydrocoumarin (1-5 mM) increases cytotoxicity in the TK6 cell line in a dose-dependent manner following a 24-h exposure. Dihydrocoumarin (1-5 mM) increases apoptosis in a dose-dependent manner in the TK6 cell line at the 6-h time point. A 5-mM dose of Dihydrocoumarin increases apoptosis at the 6-h time point in the TK6 cell line[1].Dihydrocoumarin (1-5 mM) increases p53 lysine 373 and 382 acetylation in a dose-dependent manner in the TK6 cell line following a 24-h exposure period[1].

[1]. Olaharski AJ, et al. The flavoring agent Dihydrocoumarin reverses epigenetic silencing and inhibits sirtuindeacetylases. PLoS Genet. 2005 Dec;1(6):e77.

 

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