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Dihydrocoumarin/二氢香豆素 {[allProObj[0].p_purity_real_show]}

货号:A521655 同义名: 苯并二氢吡喃-2-酮;1,2-苯并二氢吡喃酮 / Hydrocoumarin; Chroman-2-one

Dihydrocoumarin, a natural product isolated and purified from the leaves of Southern sweet-grass., is widespread used as a flavoring agent in beverages, gelatins, puddings, candy, and other food items. It is also as a fragrance in perfumes, creams, and cosmetics.

Dihydrocoumarin/二氢香豆素 化学结构 CAS号:119-84-6
Dihydrocoumarin/二氢香豆素 化学结构
CAS号:119-84-6
Dihydrocoumarin/二氢香豆素 3D分子结构
CAS号:119-84-6
Dihydrocoumarin/二氢香豆素 化学结构 CAS号:119-84-6
Dihydrocoumarin/二氢香豆素 3D分子结构 CAS号:119-84-6
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Dihydrocoumarin/二氢香豆素 纯度/质量文件 产品仅供科研

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Selisistat ++++

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99%+
Tenovin-3 p53 99%+
3-TYP ++++

SIRT1, IC50: 88 nM

++++

SIRT2, IC50: 92 nM

++++

SIRT3, IC50: 16 nM

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Tenovin-6 ++

SIRT1, IC50: 21 μM

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SIRT2, IC50: 10 μM

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SIRT3, IC50: 67 μM

p53 99%+
SirReal2 +++

SIRT2, IC50: 140 nM

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Thiomyristoyl ++++

SIRT2, IC50: 28 nM

99%+
Et-29 98%
OSS_128167 +

SIRT1, IC50: 1578 μM

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SIRT2, IC50: 751 μM

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SIRT6, IC50: 89 μM

98%
SIRT7 inhibitor 97491 +++

SIRT7, IC50: 325 nM

97%
Nicotinamide 99+%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Dihydrocoumarin/二氢香豆素 生物活性

描述 Dihydrocoumarin (DHC) is an inhibitor of the Sirtuin family of NAD+-dependent deacetylases[3]. Dihydrocoumarin also inhibits human SIRT1 and SIRT2 with IC50s of 208 μM and 295 μM, respectively. The microtubule SIRT2 deacetylase is also inhibited with a similar dose dependency (IC50 of 295 μM). 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. 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[4]. Dihydrocoumarin disrupted heterochromatic silencing and inhibited yeast Sir2p as well as human SIRT1 deacetylase activity. DHC exposure in the human TK6 lymphoblastoid cell line also caused concentration-dependent increases in p53 acetylation and cytotoxicity[4].

Dihydrocoumarin/二氢香豆素 参考文献

[1]Haser K, Wenk HH, Schwab W. Biocatalytic production of dihydrocoumarin from coumarin by Saccharomyces cerevisiae. J Agric Food Chem. 2006 Aug 23;54(17):6236-40.

[2]Olaharski AJ, Rine J, et al. The flavoring agent dihydrocoumarin reverses epigenetic silencing and inhibits sirtuin deacetylases. PLoS Genet. 2005 Dec;1(6):e77.

[3]Jacobi JL, Yang B, Li X, Menze AK, Laurentz SM, Janle EM, Ferruzzi MG, McCabe GP, Chapple C, Kirchmaier AL. Impacts on Sirtuin Function and Bioavailability of the Dietary Bioactive Compound Dihydrocoumarin. PLoS One. 2016 Feb 16;11(2):e0149207

[4]Olaharski AJ, Rine J, Marshall BL, Babiarz J, Zhang L, Verdin E, Smith MT. The flavoring agent dihydrocoumarin reverses epigenetic silencing and inhibits sirtuin deacetylases. PLoS Genet. 2005 Dec;1(6):e77

Dihydrocoumarin/二氢香豆素 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

6.75mL

1.35mL

0.67mL

33.75mL

6.75mL

3.37mL

67.49mL

13.50mL

6.75mL

Dihydrocoumarin/二氢香豆素 技术信息

CAS号119-84-6
分子式C9H8O2
分子量 148.16
SMILES Code O=C1CCC2=CC=CC=C2O1
MDL No. MFCD00006881
别名 苯并二氢吡喃-2-酮;1,2-苯并二氢吡喃酮;氢化肉桂酸内酯;二氢色满酮;二羟基香豆素;苯并二氢吡喃酮;二氢香豆酯;二氢香兰素 ;Hydrocoumarin; Chroman-2-one; DHC
运输蓝冰
InChI Key VMUXSMXIQBNMGZ-UHFFFAOYSA-N
Pubchem ID 660
存储条件

In solvent -20°C:3-6个月-80°C:12个月

溶解方案 请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案一
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