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

Chemical Structure : Sunobinop

CAS No.: 1126793-40-5

Sunobinop

货号: PC-21949Not For Human Use, Lab Use Only.

Sunobinop is a potent and partial agonist of the nociceptin/orphanin FQ peptide receptor (NOP receptor) with Ki of 3.3 nM, EC50 of 4.03 nM.

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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

Sunobinop is a potent and partial agonist of the nociceptin/orphanin FQ peptide receptor (NOP receptor) with Ki of 3.3 nM, EC50 of 4.03 nM.
Sunobinop competitively inhibited [3H]-NOP-1A binding in rat-brain sections with IC50 of 7.7 nM.
Sunobinop does not activate human μ and κ receptors and is a low-affinity, weak partial agonist at human δ receptors.
Sunobinop promotes non-REM sleep in rodents and patients with insomnia.

物理化学性质&存储条件

分子量 435.57
分子式 C26H33N3O3
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

2-Quinoxalinecarboxylic acid, 4-[(3-endo)-9-(3-exo)-bicyclo[3.3.1]non-3-yl-9-azabicyclo[3.3.1]non-3-yl]-3,4-dihydro-3-oxo-

参考文献

1. Whiteside GT, et al. J Clin Invest. 2024 Jan 2;134(1):e171172.

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