1. Anti-infection Metabolic Enzyme/Protease Immunology/Inflammation NF-κB Apoptosis
  2. Bacterial Parasite Reactive Oxygen Species Apoptosis Ferroptosis
  3. Eugenol

Eugenol  (Synonyms: 丁香酚)

目录号: HY-N0337 纯度: 99.99%
COA 产品使用指南 技术支持

Eugenol是丁香中发现的精油,具有抗菌,驱虫和抗氧化活性。 Eugenol也可抑制脂质过氧化。

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Eugenol Chemical Structure

Eugenol Chemical Structure

CAS No. : 97-53-0

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规格 价格 是否有货 数量
10 mM * 1 mL in DMSO ¥550
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100 mg ¥500
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500 mg ¥900
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5 g   询价  

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Customer Review

Other Forms of Eugenol:

  • 生物活性

  • 实验参考方法

  • 纯度 & 产品资料

  • 参考文献

生物活性

Eugenol is an essential oil found in cloves with antibacterial, anthelmintic and antioxidant activity. Eugenol is shown to inhibit lipid peroxidation.

IC50 & Target

Bacterial, Parasite[1]

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
HEK293 EC50
168 μM
Compound: Eugenol
Agonist activity at human TRPA1 expressed in HEK293 cells assessed as increase in calcium influx by Fluo-4-AM dye based fluorescence assay
Agonist activity at human TRPA1 expressed in HEK293 cells assessed as increase in calcium influx by Fluo-4-AM dye based fluorescence assay
[PMID: 30878828]
HEK293 EC50
261 μM
Compound: Eugenol
Agonist activity at human TRPA1 expressed in HEK293 assessed as increase in calcium influx by two electrode voltage clamp method
Agonist activity at human TRPA1 expressed in HEK293 assessed as increase in calcium influx by two electrode voltage clamp method
[PMID: 30878828]
HL-60 IC50
23.7 mM
Compound: Eugenol
Antiproliferative activity against human HL60 cells after 2 days by MTT assay
Antiproliferative activity against human HL60 cells after 2 days by MTT assay
[PMID: 31195168]
PC-3 IC50
1 μM
Compound: Eugenol
Cytotoxicity against human PC3 cells after 72 hrs by CellTiter one aqueous solution assay
Cytotoxicity against human PC3 cells after 72 hrs by CellTiter one aqueous solution assay
[PMID: 31195168]
Peritoneal macrophage EC50
475.76 μM
Compound: 1
Cytotoxicity against BALB/c mouse peritoneal macrophages after 48 hrs by MTT assay
Cytotoxicity against BALB/c mouse peritoneal macrophages after 48 hrs by MTT assay
[PMID: 28826085]
RAW264.7 EC50
20.81 μg/mL
Compound: Eugenol
Antileishmanial activity against intracellular Leishmania infantum chagasi MHOM/BR/00/1669 amastigotes infected in mouse RAW264.7 cells assessed as inhibition of parasite growth after 48 hrs
Antileishmanial activity against intracellular Leishmania infantum chagasi MHOM/BR/00/1669 amastigotes infected in mouse RAW264.7 cells assessed as inhibition of parasite growth after 48 hrs
[PMID: 25281268]
RAW264.7 IC50
527.04 μM
Compound: 1
Cytotoxicity against mouse RAW264.7 cells after 48 hrs by MTT assay
Cytotoxicity against mouse RAW264.7 cells after 48 hrs by MTT assay
[PMID: 28826085]
RAW264.7 EC50
56.13 μg/mL
Compound: Eugenol
Antileishmanial activity against axenically cultured Leishmania infantum chagasi MHOM/BR/00/1669 promastigotes infected in mouse RAW264.7 cells assessed as inhibition of parasite growth after 48 hrs
Antileishmanial activity against axenically cultured Leishmania infantum chagasi MHOM/BR/00/1669 promastigotes infected in mouse RAW264.7 cells assessed as inhibition of parasite growth after 48 hrs
[PMID: 25281268]
体外研究
(In Vitro)

O. gratissimum 和 Eugenol 可有效抑制 H. contortus 卵,可用于处理小反刍动物的胃肠道蠕虫病。在 0.50% 的浓度下,精油和 Eugenol 表现出最大的爬虫抑制作用[1]。Eμgenol 在浓度为 250 μM 时抑制黄嘌呤-黄嘌呤氧化酶系统中超氧阴离子的产生,抑制程度为 50%。Eugenol 还能抑制 70% 的羟基自由基的产生,在浓度为 250 μM 时抑制了 46% 的程度,通过水杨酸盐羟基化为 2,3-二羟基苯甲酸盐测量的 OH 自由基形成。除抗氧化作用外,Eugenol 还通过调节 HPA 轴和脑单胺能通路来防止 RS 诱导的 IBS 样胃肠功能障碍的发展。Eμgenol (50 mg/kg) 减少 80% 的 RS 诱导的粪便颗粒增加,类似于 ondansetron。Eugenol 可减弱 80% 的应激诱导的血浆皮质酮增加,并调节 PFC 和杏仁核中的血清素能系统。Eugenol可减轻压力引起的去甲肾上腺素变化,并增强所有大脑区域的抗氧化防御系统[3]

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

体内研究
(In Vivo)

口服 Eugenol (33 mg/kg) 2 天可显著抑制膝关节水肿,并在处理结束时继续显著减轻。2 天后,经 Eugenol 处理的分枝杆菌关节炎大鼠的爪肿胀明显减轻[4]

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

Clinical Trial
分子量

164.20

Formula

C10H12O2

CAS 号
性状

液体(密度:1.067 g/cm3

颜色

Colorless to light yellow

中文名称

丁香酚;丁香油酚;丁子香酚;丁子香酸;烯丙基甲氧基苯酚;异丁香酚苯乙醚

结构分类
初始来源
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
溶解性数据
细胞实验: 

DMSO 中的溶解度 : ≥ 100 mg/mL (609.00 mM; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

* "≥" means soluble, but saturation unknown.

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 6.0900 mL 30.4499 mL 60.8999 mL
5 mM 1.2180 mL 6.0900 mL 12.1800 mL
查看完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,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,请在6个月内使用,-20°C储存时,请在1个月内使用。

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量
=
浓度
×
体积
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

动物实验:

请根据您的 实验动物和给药方式 选择适当的溶解方案。

以下溶解方案都请先按照 In Vitro 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

  • 方案 一

    请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 3.25 mg/mL (19.79 mM); 澄清溶液

    此方案可获得 ≥ 3.25 mg/mL(饱和度未知)的澄清溶液。

    1 mL 工作液为例,取 100 μL 32.5 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;再向上述体系中加入 50 μL Tween-80,混合均匀;然后再继续加入 450 μL 生理盐水 定容至 1 mL

    生理盐水的配制:将 0.9 g 氯化钠,溶解于 ddH₂O 并定容至 100 mL,可以得到澄清透明的生理盐水溶液。
  • 方案 二

    请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 3.25 mg/mL (19.79 mM); 澄清溶液

    此方案可获得 ≥ 3.25 mg/mL(饱和度未知)的澄清溶液。

    1 mL 工作液为例,取 100 μL 32.5 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。

    2 g SBE-β-CD(磺丁基醚 β-环糊精)粉末定容于 10 mL 的生理盐水中,完全溶解至澄清透明。
动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量
请输入您的动物体内配方组成:
%
DMSO +
+
%
Tween-80 +
%
Saline
如果您的动物是免疫缺陷鼠或者体弱鼠,建议 DMSO 中的在最后工作液体系中的占比尽量不超过 2%。
方案所需 助溶剂 包括:DMSO ,均可在 MCE 网站选购。 Tween 80,均可在 MCE 网站选购。
计算结果
工作液所需浓度 : mg/mL
储备液配制方法 : mg 药物溶于 μL  DMSO(母液浓度为 mg/mL)。
您所需的储备液浓度超过该产品的实测溶解度,以下方案仅供参考,如有需要,请与 MCE 中国技术支持联系。
动物实验体内工作液的配制方法 : 取 μL DMSO 储备液,加入 μL  μL ,混合均匀至澄清,再加 μL Tween 80,混合均匀至澄清,再加 μL 生理盐水
连续给药周期超过半月以上,请谨慎选择该方案。
请确保第一步储备液溶解至澄清状态,从左到右依次添加助溶剂。您可采用超声加热 (超声清洗仪,建议频次 20-40 kHz),涡旋吹打等方式辅助溶解。
纯度 & 产品资料

纯度: 99.99%

参考文献
Cell Assay
[1]

The essential oil and eugenol are diluted in aqueous solution of Tween 20 (0.5%) in the following concentrations: 0.0625, 0.12, 0.25, 0.5 and 1.0% to be used in the egg hatch test[1].

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

Animal Administration
[4]

Rats: The treatment groups of arthritic rats are given either ingwerol (0.33 mL/kg or 33 mg/kg) or eugenol (0.33 mL/kg or 33 mg/kg) orally 1 day prior to the induction of arthritis. This treatment is continued for 26 days on a daily basis. Mycobaterium trated rats receive physiological saline orally[4].

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

参考文献

完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,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,请在6个月内使用,-20°C储存时,请在1个月内使用。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 6.0900 mL 30.4499 mL 60.8999 mL 152.2496 mL
5 mM 1.2180 mL 6.0900 mL 12.1800 mL 30.4499 mL
10 mM 0.6090 mL 3.0450 mL 6.0900 mL 15.2250 mL
15 mM 0.4060 mL 2.0300 mL 4.0600 mL 10.1500 mL
20 mM 0.3045 mL 1.5225 mL 3.0450 mL 7.6125 mL
25 mM 0.2436 mL 1.2180 mL 2.4360 mL 6.0900 mL
30 mM 0.2030 mL 1.0150 mL 2.0300 mL 5.0750 mL
40 mM 0.1522 mL 0.7612 mL 1.5225 mL 3.8062 mL
50 mM 0.1218 mL 0.6090 mL 1.2180 mL 3.0450 mL
60 mM 0.1015 mL 0.5075 mL 1.0150 mL 2.5375 mL
80 mM 0.0761 mL 0.3806 mL 0.7612 mL 1.9031 mL
100 mM 0.0609 mL 0.3045 mL 0.6090 mL 1.5225 mL
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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