Caffeine

目录号: GN10350纯度: >98.00%同义词: 咖啡因,Methyltheobromine, NSC 5036

一种甲基黄嘌呤生物碱。


Caffeine
Cas No.: 58-08-2
规格价格库存数量操作
20mg¥485.00现货
1
10mM (in 1mL DMSO)¥508.00现货
1

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产品描述 Description

Caffeine is a methylxanthine alkaloid naturally found in various plant parts that acts as an antagonist at central adenosine receptors at relevant physiological concentrations (IC50 = ~30 μM).[1],2 It alters fatigue, mood, alertness, motor reaction time, vascular hemodynamics, and pain sensation.[2],[3],[4] Caffeine has also been implicated in carcinogenesis, although the concentrations used to affect cell cycling and apoptosis in the laboratory may not be commonly achieved in vivo.[5]

咖啡因是一种甲基黄嘌呤生物碱,自然存在于各种植物部位中,在相关的生理浓度下(IC50 = ~30 μM)作为中枢腺苷受体的拮抗剂。它改变疲劳、情绪、警觉性、运动反应时间、血管血流动力学和疼痛感觉。咖啡因也被认为与癌症发生有关,尽管实验室用于影响细胞周期和凋亡的浓度可能在体内不常见。

Reference:
[1]. Snyder, S.H., Katims, J.J., Annau, Z., et al. Adenosine receptors and behavioral actions of methylxanthines. Proc. Natl. Acad. Sci. USA 78(5), 3260-3264 (1981).
[2]. Fredholm, B.B., Bättig, K., Holmén, J., et al. Actions of caffeine in the brain with special reference to factors that contribute to its widespread use. Pharmacological Reviews 51(1), 83-133 (1999).
[3]. Carrillo, J.A., and Benitez, J. Clinically significant pharmacokinetic interactions between dietary caffeine and medications. Clinical Pharmacokinetics 39(2), 127-153 (2000).
[4]. Pelligrino, D.A., Xu, H.L., and Vetri, F. Caffeine and the control of cerebral hemodynamics. J.Alzheimers Dis. 20, S51-S62 (2010).
[5]. Bode, A.M., and Dong, Z. The enigmatic effects of caffeine in cell cycle and cancer. Cancer Letters 247(1), 26-39 (2007).

实验参考方法 Experimental Reference Method

Cell experiment [1]:

Cell lines

Patient-derived AC-UPS01 and AC-RMS01 cell lines

Preparation method

The solubility of this compound in DMSO is >10 mM. General tips for obtaining a higher concentration: Please warm the tube at 37℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months.

Reacting condition

0.25, 0.5, 1, 2.5 and 5 mM; 72 h

Applications

Caffeine significantly inhibited the patient-derived UPS and RMS cell lines in a dose-dependent manner with IC50 values of 2.02 ± 0.22 mM and 2.37 ± 0.48 mM, respectively. Addition of 0.3 mM or 0.6 mM VPA to varying concentrations of CAF enhanced efficacy against both the AC-UPS01 and AC-RMS01 cell lines.

Animal experiment [2]:

Animal models

diet-induced obesity (DIO) mice

Dosage form

10 μg per mouse, i.c.v. administration

Application

In diet-induced obesity (DIO) mice, administration of caffeine into mouse brain significantly increased the numbers of c-Fos+ cells in the PVN, Arc and DMH nuclei, suggesting that caffeine stimulated the activities of neurons in the hypothalamic nuclei involved in energy balance control. Caffeine reduced the adipocyte sizes of epididymal white adipose tissue, plasma triglycerides (TG) levels and improved glucose tolerance. Mice gained significantly less body weights than the controls on day 7.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

[1] Igarashi K1,2,3, Kawaguchi K1,2, Kiyuna T1,2, et al. Efficacy In Vitro of Caffeine and Valproic Acid on Patient-Derived Undifferentiated Pleomorphic Sarcoma and Rhabdomyosarcoma Cell Lines. Anticancer Res. 2017 Aug;37(8):4081-4084.

[2] Wu L1, Meng J1, Shen Q1, et al. Caffeine inhibits hypothalamic A1R to excite oxytocin neuron and ameliorate dietary obesity in mice. Nat Commun. 2017 Jun 27;8:15904.

产品文档 Product Documents

Purity:>98.00%

化学性质Chemical Properties

CAS 号
58-08-2
同义词
咖啡因,Methyltheobromine, NSC 5036
化学名
1,3,7-trimethylpurine-2,6-dione
SMILES
CN1C=NC2=C1C(=O)N(C(=O)N2C)C
分子式
C8H10N4O2
分子量
194.19 g/mol
溶解性
0.2mg/mL in ethanol, 3mg/mL in DMSO, 10mg/mL in DMF; 33.3mg/ml in Water(Need ultrasonic)
保存条件
Store at -20°C
General tips
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 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol