Endomorphin 1 acetate

CAS: 1276123-71-7 货号: E650817 分子式: C36H42N6O7 分子量: 670.75
有货
级别和纯度: ≥99%
别名
内吗啡肽-1醋酸盐
储存条件
避光,充氩,干燥,-80℃储存
运输条件
特低温运输
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规格
库存
价格
数量
5mg
E650817-5mg
期货 Stock Image
¥550.90
10mg
E650817-10mg
期货 Stock Image
¥770.90
25mg
E650817-25mg
期货 Stock Image
¥1,320.90
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为什么选择此级别

提供 ≥99% 纯度,适用于对基线干扰要求严格的色谱和分析工作流程。

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储存与运输

避光,充氩,干燥,-80℃储存。特低温运输 。请查阅批次 COA 获取详细规格。

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质量文档

SDS、COA、产品数据表及规格说明书均可下载。可通过批号查询获取批次 COA。

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文献证明

在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。

概述


Endomorphin 1 acetate, a high affinity, highly selective agonist of the μ-opioid receptor ( K i : 1.11 nM), displays reasonable affinities for kappa 3 binding sites, with K i value between 20 and 30 nM. Endomorphin 1 acetate has antinociceptive properties.

In Vitro

Endomorphin 1 acetate inhibits Forskolin (1 μM) stimulated cyclic AMP formation with a pIC 50 value of 8.03 in In CHOμ cells . Endomorphin 1 (1-10 μM) acetate increases interleukin-8 secretion in Caco-2 cells. Endomorphin 1 (1 μM) acetate inhibits excitatory transmission in adult rat substantia gelatinosa neurons. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Endomorphin 1 (i.c.v.) acetate shows antinociceptive properties in mice, with an ED 50 value of 6.16 nM. Endomorphin 1 (50 μg/kg, i.v., rats) acetate alleviates myocardial ischemia/reperfusion injury (MIRI) by inhibiting the inflammatory response. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: ICR mice. Dosage: 6.16 nM (ED 50 ) Administration: Intracerebroventricularly (i.c.v.) injection Result: Inhibited dose-dependently the tail-flick response. Animal Model: Rats. Dosage: 50 μg/kg Administration: Intravenously following LAD ligation for 25 min, subsequently the LAD was reperfused for 120 min. Result: Alleviated MIRI by reducing the production of free radicals. Dncreased LDH and CK-MB activities. Increased SOD activity and decreased MDA content. Decreased IL-6 and TNF-α plasma content.

Form:Solid

IC50& Target:μ Opioid Receptor/MOR 1.11 nM (Ki)

规格

别名
内吗啡肽-1醋酸盐
规格或纯度
≥99%
英文名称
Endomorphin 1 acetate
生化机理
醋酸恩多吗啡 1 是一种高亲和力、高选择性的μ-阿片受体激动剂(K i:1.11 nM),对卡帕 3 结合位点具有合理的亲和力,K i 值介于 20 至 30 nM 之间。醋酸内多啡肽 1 具有抗痛觉特性
储存条件
避光,充氩,干燥,-80℃储存
运输条件
特低温运输
作用类型
激动剂
纯度
≥99%
名称和识别符
分子类型
小分子
分子量
670.75

技术文档

📋 安全数据表 (SDS)

全面的危险、操作、储存及法规合规文件。

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✅ 分析证书 (COA)

批次质量数据。输入批号以获取对应 COA。

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📊 产品数据表

产品规格和应用的快速参考摘要。

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🔬 规格说明书

该级别的完整质量属性和验收标准。

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高级数据

化学和物理性质
溶解性
DMSO : 125 mg/mL (186.36 mM; Need ultrasonic)
质检证书(CoA,COO,BSE/TSE 和分析图谱)
C of A & Other Certificates(BSE/TSE, COO):
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溶液计算器