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156727-74-1

中文名称 (+)-4-[(ΑR)-Α-((2S,5R)-4-烯丙基-2,5-二甲基-1-哌嗪基)-3-甲氧基苄基]-N,N-二乙基苯酰胺
英文名称 SNC 80
CAS 156727-74-1
分子式 C28H39N3O2
分子量 449.63
MOL 文件 156727-74-1.mol
更新日期 2023/03/20 15:41:23
156727-74-1 结构式 156727-74-1 结构式

基本信息

中文别名
(+)-4-[(ΑR)-Α-((2S,5R)-4-烯丙基-2,5-二甲基-1-哌嗪基)-3-甲氧基苄基]-N,N-二乙基苯酰胺
4-[(R)-[(2S,5R)-2,5-二甲基-4-(2-丙烯-1-基)-1-哌嗪基](3-甲氧基苯基)甲基]-N,N-二乙基苯甲酰胺
英文别名
SNC 80
NIH 10815
(+)-4-[(Ar)-alpha-((2s,5r)-4-allyl-2,5-dimethyl-1-piperazinyl)-3
4-(alpha-(4-allyl-2,5-dimethyl-1-piperazinyl)-3-methoxybenzyl)-N,N-diethylbenzamide
(+)-4-[(AR)-A-((2S,5R)-4-ALLYL-2,5-DIMETHYL-1-PIPERAZINYL)-3-METHOXYBENZYL]-N,N-DIETHYLBENZAM
(+)-4-[(aR)-α-((2S,5R)-4-Allyl-2,5-dimethyl-1-piperazinyl)-3-methoxybenzyl]-N,N-diethylbenzamide
(+)-4-[(αr)-α-((2s,5r)-4-allyl-2,5-dimethyl-1-piperazinyl)-3-methoxybenzyl]-n,n-diethylbenzamide
(+)-4-[(AR)-A-((2S,5R)-4-ALLYL-2,5-DIMETHYL-1-PIPERAZINYL)-3-METHOXYBENZYL]-N,N-DIETHYLBENZAMIDE
(+)-4-[(AR)-ALPHA-((2S,5R)-4-ALLYL-2,5-DIMETHYL-1-PIPERAZINYL)-3-METHOXYBENZYL]-N,N-DIETHYLBENZAMIDE
(+)-4-[(alphaR)-alpha-((2S,5R)-4-Allyl-2,5-dimethyl-1-piperazinyl)-3-methoxybenzyl]-N,N-diethylbenzamide

物理化学性质

熔点122-123°C
沸点564.8±50.0 °C(Predicted)
密度1.040
储存条件Store at RT
溶解度DMSO: soluble
溶解度可溶于DMSO
酸度系数(pKa)7.29±0.10(Predicted)
形态solid
颜色off-white
稳定性冷冻储存
InChIKeyKQWVAUSXZDRQPZ-UMTXDNHDSA-N
SMILESC(N(CC)CC)(=O)C1=CC=C([C@@H](N2C[C@@H](C)N(CC=C)C[C@@H]2C)C2=CC=CC(OC)=C2)C=C1

应用领域

用途1
A highly selective and potent non-peptide 鈭?agonist, 2000-fold selective over u-receptors.

安全数据

WGK Germany3
WGK Germany3

常见问题列表

生物活性
SNC80 (NIH 10815) 是一种有效的,高度选择性的非肽类 δ 阿片 (δ-opioid) 受体激动剂,Ki 为1.78 nM,IC50 为 2.73 nM。SNC80 还以 EC50 为 52.8 nM 来选择性激活 HEK293 细胞中的 μ-δ 异聚体。SNC80 具有抗伤害性,抗痛觉过敏和抗抑郁样作用,并可用于多种头痛症的研究。
靶点

IC50: 2.73 nM (δ-opioid receptor), 5457 nM (μ-opioid receptor)
Ki: 1.78 nM (δ-opioid receptor), 881.5 nM (μ-opioid receptor) and 441.8 nM (κ-opioid receptor)

体外研究

SNC80 selectively activates μ-δ heteromer in HEK293 cells with an EC 50 of 52.8 nM. SNC80 exhibits substantially greater activity in cells coexpressing μ- and δ-opioid receptors than in cells either singly expressing δ-opioid receptors or coexpressing δ- and κ-opioid receptors.

体内研究

SNC80 (10 mg/kg; intraperitoneal injection; once; C57BL6/J mice) treatment significantly attenuated this allodynia caused by overuse of Sumatriptan.

Animal Model: Male and female C57BL6/J mice (20-30g) injected with Sumatriptan
Dosage: 10 mg/kg
Administration: Intraperitoneal injection; once
Result: Significantly attenuated allodynia.
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