PD-168077 maleate 促销 ≥98%
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| 包装规格: | 100mg in glass bottle |
| 溶解性: | 溶于DMSO(150mg/mL 超声) |
| 产品描述: | 基本信息 产品编号: P11012 产品名称: PD-168077 maleate CAS: 630117-19-0 储存条件 粉末 -20℃ 四年 分子式: C24H26N4O5 溶于液体 -80℃ 6个月 分子量: 450.49 -20℃ 1个月 化学名: Benzamide,N-[[4-(2-cyanophenyl)-1-piperazinyl]methyl]-3-methyl-,(2Z)-2-butenedioate (1:1);PD 168077 maleate Solubility (25°C): 体外: DMSO Ethanol Water 体内(现配现用): <1mg/ml表示微溶或不溶。 普西唐提供的所有化合物浓度为内部测试所得,实际溶液度可能与公布值有所偏差,属于正常的批间细微差异现象。 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。 制备储备液 浓度 溶液体积 质量 1mg 5mg 10mg 1mM 2.2198mL 11.0990mL 22.1981mL 5mM 0.4440mL 2.2198mL 4.4396mL 10mM 0.2220mL 1.1099mL 2.2198mL 生物活性 产品描述 一个选择性的多巴胺 D4 受体激动剂,其 Ki 值为 9nM。 靶点 Ki:9nM (Dopamine D4 receptor) 体外研究 PD-168077 is one of the first agents to be identified as putative selective D4 agonists.It shows>100-fold selectivity over other members of the D2-like receptor family and over their D1-like counterparts;PD-168077 shows a 20-fold selectivity over α1,andα2, a 45-fold selectivity over 5-HT1A,and a 460-fold selectivity over 5-HT2A receptors;PD-168077 evidences intrinsic activity at the D4 receptor in terms of quinpirole-like inhibition of forskolin-stimulated cAMP accumulation or stimulation of [3H]thymidine uptake in CHO cells expressing the human D4 receptor.In the PD-168077-treated cell,p-CaMKII exhibits a significantly increased clustering at synaptic sites,as indicated by the enhanced colocalization with PSD-95. 体内研究 PD-168077 (0.2-25.0mg/kg) dose-dependently induces locomotion,which takes an unusual and characteristic”shuffling”form with uncoordinated movements together with yawning,and episodes of myoclonic jerking;grooming, and rearing are reduced. |
| 保存条件: | -20℃ |
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