Angiotensin (1-7) (acetate) Ang-(1-7 (acetate))|cas:2855063-75-9|西域试剂

Angiotensin (1-7) (acetate) Ang-(1-7 (acetate)),98.91%

产品编号：Bellancom-12403A| CAS NO：2855063-75-9| 分子式：C₄₃H₆₆N₁₂O₁₃| 分子量：959.06

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货号	价格	库存与货期
Bellancom-12403A	￥520.00	杭州北京（现货）
Bellancom-12403A	￥810.00	杭州北京（现货）
Bellancom-12403A	￥1800.00	杭州北京（现货）
Bellancom-12403A	￥2850.00	杭州北京（现货）

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Angiotensin (1-7) (acetate) Ang-(1-7 (acetate))

产品介绍

Angiotensin 1-7 (Ang-(1-7)) acetate 是肾素-血管紧张素系统 (RAS) 中的一种内源性七肽，由于其在心肌细胞中的抗炎和抗纤维化活性而具有心脏保护作用。Angiotensin 1-7 acetate 抑制纯化的犬血管紧张素转换酶 (ACE) 活性(IC₅₀=0.65 μM)。Angiotensin 1-7 acetate 通过抑制血管紧张素转换酶和释放一氧化氮作为激肽诱导的血管舒张的局部协同调节剂。Angiotensin 1-7 acetate 阻断血管紧张素 Ⅱ 诱导的平滑肌细胞增殖和肥大，对内皮细胞具有抗血管生成和生长抑制作用。

生物活性

Angiotensin 1-7 (Ang-(1-7)) acetate is an endogenous heptapeptide from the renin-angiotensin system (RAS) with a cardioprotective role due to its anti-inflammatory and anti-fibrotic activities in cardiac cells. Angiotensin 1-7 acetate inhibits purified canine ACE activity (IC₅₀=0.65 μM). Angiotensin 1-7 acetate acts as a local synergistic modulator of kinin-induced vasodilation by inhibiting ACE and releasing nitric oxide. Angiotensin 1-7 acetate blocks Ang II-induced smooth muscle cell proliferation and hypertrophy and shows antiangiogenic and growth-inhibitory effects on the endothelium.

体外研究

Angiotensin 1-7 (Ang-(1-7)) inhibits cultured vascular smooth muscle cell growth, whereas equal molar concentration of Ang II stimulates cell growth.
Angiotensin 1-7 (Ang 1-7) abrogates the methylglyoxal-modified albumin (MGA)-stimulated myofibroblast phenotype by inhibiting the chronic stimulation of the TGF-β-ERK pathway in NRK-52E cells^[4].
Angiotensin 1-7 signals through the Mas receptor ( MasR) in opposition to Ang II/angiotensin II type 1 receptor (AT1R), promoting anti-inflammatory,vasodilatory, and neuroprotective effects^[5].

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究

Daily Angiotensin 1-7 (Ang-(1-7)) treatment (0.01-0.06 mg/kg) results in significant amelioration of DSS-induced colitis. Colitis-associated phosphorylation of p38, ERK1/2 and Akt is reduced by Ang 1-7 treatment.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

性状

Solid

溶解性数据

In Vitro:

H₂O : 62.5 mg/mL (65.17 mM; Need ultrasonic)

配制储备液

浓度溶剂体积质量	1 mg	5 mg	10 mg

1 mM	1.0427 mL	5.2134 mL	10.4269 mL
5 mM	0.2085 mL	1.0427 mL	2.0854 mL
10 mM	0.1043 mL	0.5213 mL	1.0427 mL

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液；一旦配成溶液，请分装保存，避免反复冻融造成的产品失效。
储备液的保存方式和期限：-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-80°C 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液，再依次添加助溶剂：

——为保证实验结果的可靠性，澄清的储备液可以根据储存条件，适当保存；体内实验的工作液，建议您现用现配，当天使用；以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比；如在配制过程中出现沉淀、析出现象，可以通过加热和/或超声的方式助溶