Home>>Analytical Standards>>PRL-8-53 (hydrochloride)

PRL-8-53 (hydrochloride) Sale

目录号 : GC44683

An Analytical Reference Standard

PRL-8-53 (hydrochloride) Chemical Structure

Cas No.:51352-87-5

规格 价格 库存 购买数量
10mg
¥428.00
现货

电话:400-920-5774 Email: sales@glpbio.cn

Customer Reviews

Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.

产品文档

Quality Control & SDS

View current batch:

产品描述

PRL-8-53 (hydrochloride) is an analytical reference standard that is categorized as a phenethylamine and a nootropic. This product is intended for research and forensic applications.

Chemical Properties

Cas No. 51352-87-5 SDF
Canonical SMILES CN(CCC1=CC=CC(C(OC)=O)=C1)CC2=CC=CC=C2.Cl
分子式 C18H21NO2•HCl 分子量 319.8
溶解度 DMF: 30 mg/ml,DMSO: 30 mg/ml,Ethanol: 30 mg/ml,PBS (pH 7.2): 10 mg/ml 储存条件 Store at -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。
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。

溶解性数据

制备储备液
1 mg 5 mg 10 mg
1 mM 3.127 mL 15.6348 mL 31.2695 mL
5 mM 0.6254 mL 3.127 mL 6.2539 mL
10 mM 0.3127 mL 1.5635 mL 3.127 mL
  • 摩尔浓度计算器

  • 稀释计算器

  • 分子量计算器

质量
=
浓度
x
体积
x
分子量
 
 
 
*在配置溶液时,请务必参考产品标签上、MSDS / COA(可在Glpbio的产品页面获得)批次特异的分子量使用本工具。

计算

动物体内配方计算器 (澄清溶液)

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
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

Research Update

PRL-8-53: enhanced learning and subsequent retention in humans as a result of low oral doses of new psychotropic agent

Psychopharmacology (Berl) 1978 Apr 11;56(3):249-53.PMID:418433DOI:10.1007/BF00432846

The effect of 3-(2-benzylmethylaminoethyl) benzoic acid methyl ester hydrochloride (PRL-8-53) on learning and on retention of verbal information in human subjects was investigated. Using the serial anticipation method under double-blind conditions it was found that PRL-8-53 causes slight improvement of acquisition. Retinetion of verbal information was found improved to a statistically significant degree (most P values better than 0.01, some better than 0.001). No significant changes were found for either visual reaction time or motor control after drug when compared with placebo values.