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首页-小分子抑制剂&激动剂-GPCR-Opioid Receptor-ADL5859
ADL5859

Chemical Structure : ADL5859

CAS No.: 850173-95-4

ADL5859 (ADL-5859, ADL 5859)

货号: PC-43352Not For Human Use, Lab Use Only.

ADL5859 is a potent, selective, orally bioavailable full agonist of δ opioid receptor (DOR) with Ki of 0.84 nM and EC50 of 20 nM.

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

生物&药学活性

ADL5859 is a potent, selective, orally bioavailable full agonist of δ opioid receptor (DOR) with Ki of 0.84 nM and EC50 of 20 nM.
ADL5859 exhibits >1,000-fold selectivity for δ over µ and κ opioid receptors in both receptor binding and in vitro bioassays.
ADL5859 demonstrates analgesic and antidepressive effects in the rat and represent potential drug for chronic pain treatment, significantly reduces inflammatory and neuropathic pain, does not induce either hyperlocomotion or receptor internalization in vivo.

物理化学性质&存储条件

分子量 428.9517
分子式 C24H29ClN2O3
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

Benzamide, N,N-diethyl-4-(5-hydroxyspiro[2H-1-benzopyran-2,4'-piperidin]-4-yl)-, hydrochloride (1:1)

参考文献

1. Le Bourdonnec B, et al. J Med Chem. 2008 Oct 9;51(19):5893-6.

2. Nozaki C, et al. J Pharmacol Exp Ther. 2012 Sep;342(3):799-807.

3. Huang P, et al. Eur J Pharmacol. 2016 Jun 15;781:53-9.

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