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Spiperone

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纯度: 99.91%

货号 T0280Cas号 749-02-0

别名 螺哌隆, Spiropitan, Spiroperidol

Spiperone (Spiropitan) 是多巴胺 D2、血清素5-HT1A 和血清素5-HT2A 拮抗剂。它是广泛使用的药理学工具。它具有研究神经系统疾病的潜力。

Spiperone
其他形式的 “Spiperone”:

Spiperone

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Rating icon 很棒

纯度: 99.91%

货号 T0280 别名 螺哌隆, Spiropitan, SpiroperidolCas号 749-02-0

Spiperone (Spiropitan) 是多巴胺 D2、血清素5-HT1A 和血清素5-HT2A 拮抗剂。它是广泛使用的药理学工具。它具有研究神经系统疾病的潜力。

规格价格库存数量
1 mg
¥ 142
现货
5 mg
¥ 287
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10 mg
¥ 407
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25 mg
¥ 658
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50 mg
待询
现货
1 mL x 10 mM (in DMSO)
¥ 387
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产品介绍


Spiperone AI Summary
Spiperone exhibits significant binding affinities and bioactivities across various serotonin and dopamine receptors, as well as other targets. It shows high affinity for the rat 5-hydroxytryptamine 2 receptor (Ki = 1.0 nM) and the dopamine receptor D2 (Ki = 0.045 nM). Additionally, it has moderate to high binding affinity for several other serotonin receptors including 5-HT1A, 5-HT7, and 5-HT2A, with Ki values of 30.0 nM, 19.95 nM, and 1.8 nM, respectively. The compound also exhibits strong inhibitory activity against dopamine D3 and D4 receptors with Ki values of 0.25 nM and 0.33 nM, respectively, and demonstrates potential multi-target activity across dopaminergic and serotonergic systems. Furthermore, Spiperone shows high potency in displacing radioligands from dopamine D2 receptors (IC50 = 0.06 nM) and a significant selectivity towards these receptors compared to others. In terms of adrenergic receptors, it displays notable affinity for the Alpha-1A adrenergic receptor (Ki = 7.2 nM). The compound has demonstrated cardiotoxic effects, such as QTc prolongation in guinea pigs, and exhibits various bioactivities, including inhibition of sodium fluorescein uptake and displacement of [3H]BTX-B from sodium channels. It has also shown antiviral activity, inhibiting SARS-CoV-2 replication in vitro with IC50 values around 20400.0 nM. Overall, the diverse range of bioactivities associated with Spiperone suggests its potential therapeutic applications in neurological disorders, psychiatric conditions, and possibly antiviral treatments, while also highlighting the need for careful consideration of its cardiotoxicity and broad receptor interactions..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Spiperone (Spiropitan) is a spiro butyrophenone analog similar to HALOPERIDOL and other related compounds. It has been recommended in the treatment of SCHIZOPHRENIA.
别名螺哌隆, Spiropitan, Spiroperidol
化学信息
分子量395.47
分子式C23H26FN3O2
CAS No.749-02-0
SmilesFc1ccc(cc1)C(=O)CCCN1CCC2(CC1)N(CNC2=O)c1ccccc1
密度1.1714 g/cm3 (Estimated)
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 25 mg/mL (63.22 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (10.11 mM), Sonication is recommended.
请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM2.5286 mL12.6432 mL25.2864 mL126.4318 mL
5 mM0.5057 mL2.5286 mL5.0573 mL25.2864 mL
10 mM0.2529 mL1.2643 mL2.5286 mL12.6432 mL
20 mM0.1264 mL0.6322 mL1.2643 mL6.3216 mL
50 mM0.0506 mL0.2529 mL0.5057 mL2.5286 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
TargetMol | Animal experiments 比如您的给药剂量是10 mg/kg,每只动物体重20g,给药体积100 μLTargetMol | Animal experiments 一共给药动物10只,您使用的配方为5%TargetMol | reagent DMSO + 30%PEG300 + 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

方案所需的各类助溶剂如: DMSOPEG300 / PEG400Tween 80SBE-β-CD玉米油 等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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