Domperidone-d6
(Synonyms: 多潘立酮 d6) 目录号 : GC47262An internal standard for the quantification of domperidone
Cas No.:1329614-18-7
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
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- Purity: >99.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Domperidone-d6 is intended for use as an internal standard for the quantification of domperidone by GC- or LC-MS. Domperidone is a dopamine D2 receptor antagonist (Ki = 0.3 nM in CHO cells expressing the rat receptor).1,2 It is selective for dopamine D2 over D3 receptors (Ki = 9.5 nM).1 Domperidone (0.5-5 µg/kg) inhibits dipropyl dopamine-induced femoral vasodilation in dogs, indicating dopamine D2 receptor antagonist activity, and has no effect on dopamine-induced vasodilation in the renal vascular bed in dogs when administered at doses up to 5 mg/kg, indicating a lack of activity at dopamine D1 receptors.2 Domperidone (0.5 mg/kg) prevents dopamine-induced decreases in gastric antral motility induced by pentagastrin in dogs.3 It inhibits apomorphine-induced emesis in dogs (ED50 = 0.031 mg/kg, p.o.).4 Domperidone also increases serum levels of prolactin in male rats.5
1.Sokoloff, P., Giros, B., Martres, M.P., et al.Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neurolepticsNature137(6289)146-151(1990) 2.Kohli, J.D., Glock, D., and Goldberg, L.I.Selective DA2 versus DA1 antagonist activity of domperidone in the peripheryEur. J. Pharmacol.89(1-2)137-141(1983) 3.Bech, K., Hovendal, C.P., and Andersen, D.Effect of dopamine on pentagastrin-stimulated gastric antral motility in dogs with gastric fistulaScand. J. Gastroenterol.17(1)103-107(1982) 4.Niemegeers, C.J.E.Antiemetic specificity of dopamine antagonistsPsychopharmacology (Berl).78(3)210-213(1982) 5.Meltzer, H.Y., Simonovic, M., and So, R.Effects of a series of substituted benzamides on rat prolactin secretion and 3H-spiperone binding to bovine anterior pituitary membranesLife Sci.32(25)2877-2886(1983)
Cas No. | 1329614-18-7 | SDF | |
别名 | 多潘立酮 d6 | ||
Canonical SMILES | ClC1=CC=C2C(NC(N2C3CCN(C([2H])([2H])C([2H])([2H])C([2H])([2H])N4C(C=CC=C5)=C5NC4=O)CC3)=O)=C1 | ||
分子式 | C22H18ClD6N5O2 | 分子量 | 432 |
溶解度 | DMSO: slightly soluble,Methanol: slightly soluble | 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。 |
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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 | 2.3148 mL | 11.5741 mL | 23.1481 mL |
5 mM | 0.463 mL | 2.3148 mL | 4.6296 mL |
10 mM | 0.2315 mL | 1.1574 mL | 2.3148 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。
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