基本信息
产品编号: |
C70262 |
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产品名称: |
Cineole |
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CAS: |
470-82-6 |
储存条件 |
粉末 |
室温 |
四年 |
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分子式: |
溶于液体 |
-20℃ |
两年 |
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分子量 |
154.25 |
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化学名: |
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Solubility (25°C): |
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体外:
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DMSO |
≥ 120mg/mL (777.96mM) |
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Ethanol |
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Water |
30mg/mL (194.4895mM; Need ultrasonic) |
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体内(现配现用): |
1.请依序添加每种溶剂:10% DMSO→40% PEG300→5% Tween-80→45% saline Solubility: ≥ 3.5mg/mL (22.69mM); Clear solution |
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此⽅案可获得 ≥ 3.5mg/mL (22.69mM,饱和度未知) 的澄清溶液。 以 1mL ⼯作液为例,取 100μL 35.0mg/mL 的澄清 DMSO 储备液加到 400μL PEG300 中,混合均匀;向上述体系中加⼊ 50μL Tween-80,混合均匀;然后继续加⼊ 450μL ⽣理盐⽔定容⾄ 1mL。 |
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2.请依序添加每种溶剂:10% DMSO→90% (20% SBE-β-CD in saline) Solubility: ≥ 3.5mg/mL (22.69mM); Clear solution |
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此⽅案可获得 ≥ 3.5mg/mL (22.69mM,饱和度未知) 的澄清溶液。 以 1mL ⼯作液为例,取 100μL 35.0mg/mL 的澄清 DMSO 储备液加到 900μL 20% 的 SBE-β-CD ⽣理盐⽔⽔溶液中,混合均匀。 |
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3.请依序添加每种溶剂:10% DMSO→90% corn oil Solubility: ≥ 3.5mg/mL (22.69mM); Clear solution |
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此⽅案可获得 ≥ 3.5mg/mL (22.69mM,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 1mL ⼯作液为例,取 100μL 35.0mg/mL 的澄清 DMSO 储备液加到 900μL ⽟⽶油中,混合均匀。 |
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<1mg/ml表示微溶或不溶。 |
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普西唐提供的所有化合物浓度为内部测试所得,实际溶液度可能与公布值有所偏差,属于正常的批间细微差异现象。 |
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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。 |
制备储备液
浓度
溶液体积 质量 |
1mg |
5mg |
10mg |
1mM |
6.4830mL |
32.4149mL |
64.8298mL |
5mM |
1.2966mL |
6.4830mL |
12.9660mL |
10mM |
0.6483mL |
3.2415mL |
6.4830mL |
生物活性
产品描述 |
Eucalyptol 是 5-HT3 受体, 钾通道, TNF-α 和 IL-1β 的抑制剂。 |
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靶点 |
5-HT3 Receptor |
IL-1β |
TNF-α |
potassium channel |
体外研究 |
Eucalyptol inhibits 5-HT-evoked currents in oocytes expressing 5-HT3 receptors with an IC50 of 258μM. Eucalyptol (Cin) treatment significantly decreases the ROS level in Aβ25-35 treated cells in a dose dependent manner. Eucalyptol treatment significantly decreases the NO level in Aβ25-35 treated cells in a dose dependent manner (p<0.01). Eucalyptol treatment also significantly decreases IL-1βlevel in Aβ25-35 treated cells in a dose dependent manner (p<0.01) as compare to Aβ25-35 treated PC12 cells. IL-6 level is also attenuated by Eucalyptol in dose dependent manner (p<0.01) as compare to Aβ25-35 treated cells |
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体内研究 |
Results show that male and female rats treated with Eucalyptol (CIN) at the highest doses, 500 and 1000mg/kg, have shown lower body weight than control group from the 7th to 50th day of treatment. The administration of Eucalyptol significantly reduces body weight gain of male rats (Eucalyptol 500 and 1000mg/kg) and female rats (Eucalyptol 1000mg/kg) in the first week of treatment. However, this reduction is followed by an increase in body weight of rats males and females treated with all doses of the second week until the end of treatment. For male rats, there is a significant increase of 6.93% in mean corpuscular volume (MCV) (Eucalyptol 1000mg/kg) and of 43.54 and 38.98% in the platelet count (Eucalyptol 500 and 1000mg/kg, respectively) and a decrease of 6.74 and 6.67% in mean corpuscular hemoglobin concentration (MCHC) (Eucalyptol 500 and 1000mg/kg) and mean platelet volume (MPV) of 10.40, 10.60 and 15.73% (Eucalyptol 100, 500 and 1000mg/kg, respectively), when compare to the control group |
推荐实验方法(仅供参考)
Cell Assay |
The protective dose of Eucalyptol (Cineole) is determined by MTT dye-uptake method. In brief, cells (1×104 per well) are seeded in 96-well tissue culture plates and allowed to adhere for 24 h in CO2 incubator at 37°C. Cells are differentiated for the indicated time period. Thereafter, the medium is replaced with the medium containing Eucalyptol (0 to 10μM) in different experiments for a period up to 24 h. Tetrazolium bromide salt (5mg/mL of stock in PBS) 10μL/well is added in 100mL of cell suspension and plate is incubated for 4 h. At the end of incubation period, the reaction mixture is carefully taken out and 200μL of DMSO is added to each well by pipetting up and down several times until the content gets homogenized. The plates are kept on rocker shaker for 10 min at room temperature and then read at 550nm using microplate reader |
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Animal Administration |
Swiss mice are used in this experiment. The animals are randomly divided into two groups (n=5) and fasted overnight with free access to water. The group control receives a 1% Tween-80 aqueous solution (0.1mL/10 g) and the other group is treated with Eucalyptol a single 2000mg/kg dose by oral route. The animals are observed at 30, 60, 120, 180 and 240 min after oral treatment and daily for 14 days. Behavioral changes, weight, food and water consumption, clinical signs of toxicity or mortality are recorded daily |
本计算器可帮助您计算出特定溶液中溶质的质量、溶液浓度和体积之间的关系,公式为:
质量 (g) = 浓度 (mol/L) x 体积 (L) x 分子量 (g/mol)
摩尔浓度计算公式
用本工具协助配置特定浓度的溶液,使用的计算公式为:
开始浓度 x 开始体积 = 最终浓度 x 最终体积
稀释公式
稀释公式一般简略地表示为:C1V1 = C2V2 ( 输入 输出 )