Theobromine-d6
(Synonyms: 可可碱-D6(二甲基-D6),3,7-Dimethylxanthine-d6) 目录号 : GC48162An internal standard for the quantification of theobromine
Cas No.:117490-40-1
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
- View current batch:
- Purity: >99.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Theobromine-d6 is intended for use as an internal standard for the quantification of theobromine by GC- or LC-MS. Theobromine is a methylxanthine alkaloid and derivative of caffeine that has been found in cocoa beans and has diverse biological activities.1,2,3 It is an adenosine A1 receptor antagonist (IC50s = 200-280 μM in radioligand binding assays using rat brain membranes).2 Theobromine (150 μg/ml) increases AMPK phosphorylation and inhibits adipocyte differentiation, ERK and JNK phosphorylation, and IL-6 and TNF-α production in 3T3-L1 preadipocytes cultured in differentiation medium.1 It inhibits decreases in renal cortex SIRT1 activity and increases in NADPH oxidase-dependent reactive oxygen species (ROS) production, as well as reduces kidney hypertrophy and albuminuria in a spontaneously hypertensive rat model of streptozotocin-induced diabetes when administered at a dose of 5 mg/kg per day.3 Theobromine is toxic to dogs with an LD50 value of 250 to 500 mg/kg.4
1.Jang, Y.J., Koo, H.J., Sohn, E.-H., et al.Theobromine inhibits differentiation of 3T3-L1 cells during the early stage of adipogenesis via AMPK and MAPK signaling pathwaysFood Funct.6(7)2365-2374(2015) 2.Daly, J.W., Butts-Lamb, P., and Padgett, W.Subclasses of adenosine receptors in the central nervous system: Interaction with caffeine and related methylxanthinesCell. Mol. Neurobiol.3(1)69-80(1983) 3.Papadimitriou, A., Silva, K.C., Peixoto, E.B.M.I., et al.Theobromine increases NAD?/Sirt-1 activity and protects the kidney under diabetic conditionsAm. J. Physiol. Renal Physiol.308(3)F209-F225(2015) 4.Lawrence, L.P.Chocolate toxicosisThe 5-minute veterinary consult: Canine and feline(2004)
Cas No. | 117490-40-1 | SDF | |
别名 | 可可碱-D6(二甲基-D6),3,7-Dimethylxanthine-d6 | ||
Canonical SMILES | O=C(C(N(C([2H])([2H])[2H])C=N1)=C1N2C([2H])([2H])[2H])NC2=O | ||
分子式 | C7H2D6N4O2 | 分子量 | 186.2 |
溶解度 | DMF: 10 mg/ml,DMSO: 10 mg/ml,Ethanol: 1 mg/ml,PBS (pH 7.2): 1 mg/ml | 储存条件 | 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℃,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。 |
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 5.3706 mL | 26.8528 mL | 53.7057 mL |
5 mM | 1.0741 mL | 5.3706 mL | 10.7411 mL |
10 mM | 0.5371 mL | 2.6853 mL | 5.3706 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。