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8-Hydroxy-DPAT hydrobromide

Synonyms: 8-OH-DPAT hydrobromide, 7-(二丙基氨基)-5,6,7,8-四氢-1-萘酚氢溴酸盐
货号 T22534Cas号 76135-31-4 一键复制产品信息纯度: 99.99%
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8-Hydroxy-DPAT hydrobromide (8-OH-DPAT hydrobromide) 是一种选择性5-HT1A 激动剂,pIC50为 8.19。它对 5-HT1结合位点的亚型有近 1000 倍的选择性。

8-Hydroxy-DPAT hydrobromide

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纯度: 99.99%

货号 T22534Cas号 76135-31-4

别名 8-OH-DPAT hydrobromide, 7-(二丙基氨基)-5,6,7,8-四氢-1-萘酚氢溴酸盐

8-Hydroxy-DPAT hydrobromide (8-OH-DPAT hydrobromide) 是一种选择性5-HT1A 激动剂,pIC50为 8.19。它对 5-HT1结合位点的亚型有近 1000 倍的选择性。

8-Hydroxy-DPAT hydrobromide
其他形式的 “8-Hydroxy-DPAT hydrobromide”:
规格价格库存数量
1 mg
¥ 185
现货
5 mg
¥ 398
现货
10 mg
¥ 663
现货
25 mg
¥ 1,390
现货
50 mg
¥ 2,570
现货
100 mg
¥ 3,870
现货
500 mg
¥ 8,530
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选择批次:
纯度: 99.96%
颜色: 白色至灰色
性状: Solid
资源下载: COA HNMR LCMS产品操作手册

产品介绍


8-Hydroxy-DPAT hydrobromide AI Summary
8-Hydroxy-DPAT hydrobromide exhibits high binding affinity at the 5-hydroxytryptamine 1A receptor, displacing [3H]8-OH-DPAT in rat brain with a Ki value of 3.18 nM, and shows potent dose-dependent effects with an ED50 value of 0.00006 mg/kg for reducing 5-HTP formation in the rat brain's limbic and striatal regions. It induces hypothermia in both Albino Swiss and CD1 mice with notable dose-dependent effects over various time points and displays antidepressant-like activity by reducing immobility time in the forced swimming test. The hypothermic effect is partially counteracted by the 5-HT1A antagonist WAY 100635. Additionally, the compound shows anxiolytic properties in Sprague-Dawley rats, increasing time spent in the open arm of the Elevated Plus Maze (EPM) test at a dose of 0.5 mg/kg. 8-Hydroxy-DPAT hydrobromide is a potent inhibitor of Bloom's syndrome helicase (BLM) with a potency of 223.9 nM and histone lysine methyltransferase G9a with a potency of 22.4 nM. It also serves as a moderate inhibitor of glutaminase (GLS) with a potency of 11220.2 nM and shows activity against Marburg Virus entry with a potency of 35481.3 nM. Despite showing some activity as an agonist of the mouse serotonin receptor 2A, it demonstrates antiviral activity against SARS-CoV-2 by inhibiting cytotoxicity in Caco-2 and VERO-6 cells at a concentration of 10 µM and by inhibiting SARS-CoV-2 3CL-Pro protease by 13.03% at 20 µM. In pharmacokinetics, 8-Hydroxy-DPAT hydrobromide has a half-life of 0.45 hours in Sprague-Dawley rat plasma when administered orally at a dose of 10 mg/kg..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
8-Hydroxy-DPAT hydrobromide (8-OH-DPAT hydrobromide) (8-OH-DPAT hydrobromide) is a potent and selective 5-HT1A agonist with a pIC50 of 8.19. 8-Hydroxy-DPAT hydrobromide has a selectivity of almost 1000 fold for a subtype of the 5-HT1 binding site.
别名
8-OH-DPAT hydrobromide, 7-(二丙基氨基)-5,6,7,8-四氢-1-萘酚氢溴酸盐
化学信息
分子量328.29
分子式C16H26BrNO
CAS No.76135-31-4
SmilesBr.CCCN(CCC)C1CCc2cccc(O)c2C1
密度no data available
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.

实际储存温度请以COA为准

溶解度信息
H2O: Soluble
DMSO: 50 mg/mL (152.3 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM3.0461 mL15.2304 mL30.4609 mL152.3044 mL
5 mM0.6092 mL3.0461 mL6.0922 mL30.4609 mL
10 mM0.3046 mL1.5230 mL3.0461 mL15.2304 mL
20 mM0.1523 mL0.7615 mL1.5230 mL7.6152 mL
50 mM0.0609 mL0.3046 mL0.6092 mL3.0461 mL
100 mM0.0305 mL0.1523 mL0.3046 mL1.5230 mL
该溶液配制表仅适用于固体产品。对于液体产品,请根据标明的浓度或密度计算稀释方案。

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:
比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL, 一共给药动物10只,您使用的配方为 10% DMSO + 40% PEG300 + 5% Tween 80 + 45% Saline / PBS / ddH2O, 那么您的工作液浓度为2 mg/mL
母液配置方法:2 mg 药物溶于 100 μL DMSO ( 母液浓度为 20 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:100 μL DMSO 母液, 添加 400 μL PEG300 混匀澄清, 再加 50 μL Tween 80, 混匀澄清, 再加 450 μL Saline / PBS / ddH2O 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: DMSOPEG300PEG400Tween 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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