Piribedil
(Synonyms: 吡贝地尔; 双哌嘧啶) 目录号 : GC36929
A dopamine receptor agonist
Cas No.:3605-01-4
Sample solution is provided at 25 µL, 10mM.
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Piribedil is a dopamine receptor agonist.1,2,3,4 It binds to dopamine D2, D3, and D4 receptors (IC50s = 1-1,000 nM in radioligand binding assays).1 Piribedil (1 and 10 mg/kg) enhances spontaneous object recognition in young adult rats and attenuates age-related memory impairments in the radial arm maze in mice.2 It reduces immobility time in the forced swim test in mice when administered at doses ranging from 0.63 to 10 mg/kg.3 Piribedil (0.3 mg/kg) decreases the number of premature and delayed responses in a response time test, indicating improved attentional function, in a rat model of Parkinson's disease induced by 6-OHDA when administered in combination with L-DOPA .4
1.Cagnotto, A., Parotti, L., and Mennini, T.In vitro affinity of piribedil for dopamine D3 receptor subtypes, an autoradiographic studyEur. J. Pharmacol.313(1-2)63-67(1996) 2.Marighetto, A., Valerio, S., Philippin, J.N., et al.Comparative effects of the dopaminergic agonists piribedil and bromocriptine in three different memory paradigms in rodentsJ. Psychopharmacol.22(5)511-521(2008) 3.Brocco, M., Dekeyne, A., Papp, M., et al.Antidepressant-like properties of the anti-Parkinson agent, piribedil, in rodents: Mediation by dopamine D2 receptorsBehav. Pharmacol.17(7)559-572(2006) 4.Turle-Lorenzo, N., Maurin, B., Puma, C., et al.The dopamine agonist piribedil with L-DOPA improves attentional dysfunction: Relevance for Parkinson's diseaseJ. Pharmacol. Exp. Ther.319(2)914-923(2006)
| Cas No. | 3605-01-4 | SDF | |
| 别名 | 吡贝地尔; 双哌嘧啶 | ||
| Canonical SMILES | C1(N2CCN(CC3=CC=C(OCO4)C4=C3)CC2)=NC=CC=N1 | ||
| 分子式 | C16H18N4O2 | 分子量 | 298.34 |
| 溶解度 | DMSO: 33.33 mg/mL (111.72 mM) | 储存条件 | Store at 4°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 | 3.3519 mL | 16.7594 mL | 33.5188 mL |
| 5 mM | 0.6704 mL | 3.3519 mL | 6.7038 mL |
| 10 mM | 0.3352 mL | 1.6759 mL | 3.3519 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
- View current batch:
- Purity: >99.50%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet