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Naringin Dihydrochalcone.

(Synonyms: 柚皮苷二氢查尔酮; Naringin DC)
目录号: PC19168 纯度: ≥98%
Naringin Dihydrochalcone是由柚皮苷衍生的人造甜味剂。 柚皮苷是从番茄,葡萄柚和许多其他柑橘类水果中获得的主要黄烷酮糖苷。
CAS No. :18916-17-1
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中文名称
Naringin Dihydrochalcone.
中文别名
柚皮苷二氢查尔酮;柚皮甙二氢查尔酮;柚皮苷二氢查耳酮;4-(2,4-二氟苯基)哌啶;柚苷二氢查耳酮;柚皮甙二氢查尔酮 Naringin dihydrochalcone;柚皮甙二氢查尔酮,Naringin dihydrochalcone,植物提取物,标准品,对照品;柚皮甙二氢查尔酮对照品;柚皮苷二氢查尔酮 标准品;柚皮苷二氢查尔酮(柚皮甙二氢查尔酮);柚皮苷二氢查尔酮对照品;高级糖精;西仑吉肽;柚苷二氢查尔酮;柚皮甙二氢查耳酮;柚皮甙二氢査尔酮;柚皮甙二氢查尔酮.柚苷二氢;柚皮苷二氢查尔酮(标准品)
英文名称
Naringin Dihydrochalcone
英文别名
Naringin dihydrochalcone;NARINGIN DIHYDOROCHALCONE;NAGINGINDIHYDROCHALCONE;Naringin DC;NARINGINDIHYDROHALCONE;1-[4-[[2-O-(6-Deoxy-L-mannopyranosyl)-D-glucopyranosyl]oxy]-2,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)-1-propanone;Senior saccharin;2,6-dihydroxyphenyl]-3-(4-hydroxyphenyl);Naringin dihydrochal;Naringin Dihydrochalcone(Naringin DC);Naringin-dihydro-chalkon;2,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)-;Senior saccharin;ranosyl)- β-D-glucopyranosyl]oxy]-;1-Propanone, 1-[4-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-2,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)-;1-[4-[(2S,3R,4S,5R,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyl
Cas No.
18916-17-1
分子式
C27H34O14
分子量
582.55
包装储存
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
详情描述

Naringin Dihydrochalcone是由柚皮苷衍生的人造甜味剂。 柚皮苷是从番茄,葡萄柚和许多其他柑橘类水果中获得的主要黄烷酮糖苷。

生物活性

Naringin Dihydrochalcone is an artificial sweetener derived from naringin. Naringin is a major flavanone glycoside obtained from tomatoes, grapefruits, and many other citrus fruits. Naringin exhibits biological properties such as antioxidant, anti-inflammatory, and antiapoptotic activities. Naringin suppresses NF-κB signaling pathway.

性状

Solid

IC50 & Target[1][2]

NF-κB

 

体外研究(In Vitro)

Naringin suppresses NF-κ B signaling pathway activation. Naringenin inhibits high glucose-induced proliferation, inflammatory reaction and oxidative stress injury in HBZY-1 cells. Naringin inhibits AGS cancer cell proliferation in a dose- and time-dependent manner. Phosphorylation of PI3K and its activated downstream targets p-Akt and p-mTOR are significantly decreased at 2 mM in Naringin-treated AGS cells. Naringin induces autophagic cell death in AGS cells. Naringin activated the autophagy related protein in AGS cells. Naringin protects PC12 cells from 3-NP neurotoxicity. The lactate dehydrogenase release is decreased upon naringin treatment in 3-NP-induced PC12 cells. Naringin treatment enhances the antioxidant defense by increasing the activities of enzymatic antioxidants and the level of reduced glutathione.

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

体内研究(In Vivo)

Treatment with naringin significantly alleviates renal injury in diabetic rats and increases diabetic rats body weight significantly. Administration of naringin effectively alleviates the collagen deposition and renal interstitial fibrosis in diabetic rats. Treatment with naringin could result in decreased levels of ROS and MDA and increased activities of SOD and GSH-Px. Oral administration of naringin significantly improves the learning and memory abilities. Naringin significantly enhances insulin signaling pathway.

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

运输条件

Room temperature or refrigerated transportation.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
结构分类
来源
参考文献
溶解度数据
体外研究: 

DMSO : ≥ 100 mg/mL (171.66 mM)

* "≥" means soluble, but saturation unknown.

配制储备溶液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.7166 mL 8.5830 mL 17.1659 mL
5 mM 0.3433 mL 1.7166 mL 3.4332 mL
10 mM 0.1717 mL 0.8583 mL 1.7166 mL
*

产品不同,其溶解度不同。建议根据产品选择合适的溶剂配制储备溶液;配成溶液后,建议分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,建议在 6 个月内使用,-20°C 储存时,建议在 1 个月内使用。

体内研究:

建议根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都建议先按照 体外研究 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,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制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

  • 1.

    建议依照次序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 10 mg/mL (17.17 mM); Clear solution

    此方案可获得 ≥ 10 mg/mL (17.17 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 100.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH?O 中,得到澄清透明的生理盐水溶液
  • 2.

    建议依照次序添加每种溶剂: 10% DMSO    90% corn oil

    Solubility: ≥ 10 mg/mL (17.17 mM); Clear solution

    此方案可获得 ≥ 10 mg/mL (17.17 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 100.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

  • 3.

    建议依照次序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (4.29 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (4.29 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液中,混合均匀。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
*
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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