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LP-211

    
≥98%

N-(4-Cyanophenylmethyl)-4-(2-diphenyl)-1-piperazinehexanamide

源叶(MedMol)
S87644 一键复制产品信息
1052147-86-0
C30H34N4O
466.62
6-(4-Biphenyl-2-yl-piperazin-1-yl)-hexanoic acid 4-cyano-benzylamide, N-(4-Cyanophenylmethyl)-4-(2-diphenyl)-1-piperazinehexanamide, N-[(4-Cyanophenyl)methyl]-4-[1,1′-biphenyl]-2-yl-1-piperazinehexan
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S87644-5mg
≥98%

¥560.00

10 - - - -
S87644-10mg
≥98%

¥880.00

5 - - - -
S87644-25mg
≥98%

¥1760.00

货期:2-3天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: LP-211 is a selective and blood−brain barrier penetrant 5-HT7 receptor agonist, with a Ki of 0.58 nM, with high selectivity over 5-HT1A receptor (Ki, 188 nM) and D2 receptor (Ki, 142 nM).
靶点: 5-HT7 Receptor:0.58 nM (Ki);5-HT1A Receptor:188 nM (Ki);D2 Receptor:142 nM (Ki);DopamineReceptor; 5-HTReceptor
体外研究: LP-211 is a selective 5-HT7 receptor agonist, with a Ki of 0.58 nM, 324- and 245-fold selectivity over 5-HT1A receptor (Ki, 188 nM) and D2 receptor (Ki, 142 nM). LP-211 shows agonist properties with an EC50 of 0.6 μM
体内研究: LP-211 (10 mg/kg, i.p.) rapidly reaches the systemic circulation in the mouse, with mean Cmax of 0.76 ± 0.32 μg/mL at 30 min. LP-211 (0.003-0.3 mg/kg, i.p.) significantly increases the micturition volume in a dose-dependent manner, and causes significant increases in voiding efficiency in spinal cord-injured (SCI) rats, and such effects can be completely reversed by SB-269970. LP-211 (0.25 and 0.50 mg/kg i.p.) improves consolidation of chamber-shape memory in rats, resulting in significant novelty-induced hyperactivity and recognition
参考文献: 1. Leopoldo M, et al. Structural modifications of N-(1,2,3,4-tetrahydronaphthalen-1-yl)-4-aryl-1-piperazinehexanamides: influence on lipophilicity and 5-HT7 receptor activity. Part III. J Med Chem. 2008 Sep 25;51(18):5813-22. 2. Norouzi-Javidan A, et al. Effect of 5-HT7 receptor agonist, LP-211, on micturition following spinal cord injury in male rats. Am J Transl Res. 2016 Jun 15;8(6):2525-33. eCollection 2016. 3. Beaudet G, et al. LP-211, a selective 5-HT7 receptor agonist, increases novelty-preference and promotes risk-prone behavior in rats. Synapse. 2017 Dec;71(12).
溶解性: Soluble  in  DMSO、Ethanol
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.143 ml 10.715 ml 21.431 ml
5 mM 0.429 ml 2.143 ml 4.286 ml
10 mM 0.214 ml 1.072 ml 2.143 ml
50 mM 0.043 ml 0.214 ml 0.429 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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