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首页-小分子抑制剂&激动剂-GPCR-5-HT Receptor-LP-211
LP-211

Chemical Structure : LP-211

CAS No.: 1052147-86-0

LP-211 (LP211)

货号: PC-73300Not For Human Use, Lab Use Only.

LP-211 is a potent, selective, and BBB-penetrant 5-HT7 receptor agonist with Ki of 0.58 nM, high selectivity over 5-HT1A receptor (Ki, 188 nM) and D2 receptor (Ki, 142 nM).

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5 mg ¥780 In stock
10 mg ¥1180 In stock
25 mg ¥2180 In stock
50 mg ¥3480 In stock
100 mg Get quote

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

LP-211 is a potent, selective, and brain penetrant 5-HT7 receptor agonist with Ki of 0.58 nM, high selectivity over 5-HT1A receptor (Ki, 188 nM) and D2 receptor (Ki, 142 nM).
LP-211 displays excellent selectivity profile over a panel of 5-HT receptor subtypes.|
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.
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 5-HT7 antagonist SB-269970.

物理化学性质&存储条件

分子量 466.629
分子式 C30H34N4O
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

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

参考文献

1. Hedlund PB, et al. Neurosci Lett. 2010 Aug 30;481(1):12-6.

2. Leopoldo M, et al. J Med Chem. 2008 Sep 25;51(18):5813-22.

3. Speranza L, et al. Neuropharmacology. 2013 Apr;67:155-67.

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