Rizatriptan-d6 (benzoate salt)
(Synonyms: 利扎曲坦苯甲酸盐 d6 (苯甲酸盐)) 目录号 : GC48583
An internal standard for the quantification of rizatriptan
Cas No.:1216984-85-8
Sample solution is provided at 25 µL, 10mM.
Rizatriptan-d6 is intended for use as an internal standard for the quantification of rizatriptan by GC- or LC-MS. Rizatriptan is an agonist of the serotonin (5-HT) receptor subtypes 5-HT1B and 5-HT1D (Kis = 4.3 and 10.1 nM, respectively).1 It is selective for 5-HT1B and 5-HT1D receptors over 5-HT1A receptors (Ki = 140 nM). Rizatriptan induces vasoconstriction in isolated human middle meningeal arteries (EC50 = 90 nM).2 In vivo, rizatriptan (50 and 75 mg/kg) reduces head grooming, the number of oculotemporal strokes, eye blinking, and one-eye closures in a Cacna1a mutant transgenic mouse model of migraine.3 Formulations containing rizatriptan have been used in the treatment of migraine.
1.Xu, Y.-C., Schaus, J.M., Walker, C., et al.N-Methyl-5-tert-butyltryptamine: A novel, highly potent 5-HT1D receptor agonistJ. Med. Chem.42(3)526-531(1999) 2.Longmore, J., Razzaque, Z., Shaw, D., et al.Comparison of the vasoconstrictor effects of rizatriptan and sumatriptan in human isolated cranial arteries: Immunohistological demonstration of the involvement of 5-HT1B-receptorsBr. J. Clin. Pharmacol.46(6)577-582(1998) 3.Chanda, M.L., Tuttle, A.H., Baran, I., et al.Behavioral evidence for photophobia and stress-related ipsilateral head pain in transgenic Cacna1a mutant micePain154(8)1254-1262(2013)
Cas No. | 1216984-85-8 | SDF | |
别名 | 利扎曲坦苯甲酸盐 d6 (苯甲酸盐) | ||
Canonical SMILES | OC(C1=CC=CC=C1)=O.[2H]C([2H])([2H])N(C([2H])([2H])[2H])CCC(C2=C3)=CNC2=CC=C3CN4C=NC=N4 | ||
分子式 | C15H13D6N5•C7H6O2 | 分子量 | 397.5 |
溶解度 | DMSO: soluble | 储存条件 | -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 | |||
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1 mg | 5 mg | 10 mg |
1 mM | 2.5157 mL | 12.5786 mL | 25.1572 mL |
5 mM | 0.5031 mL | 2.5157 mL | 5.0314 mL |
10 mM | 0.2516 mL | 1.2579 mL | 2.5157 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。
Quality Control & SDS
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- Purity: >99.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet